PUBLICACIÓN

Isolation of new nonconditional Saccharomyces cerevisiae mutants defective in asparagine-linked glycosylation

ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Mañas, P., Olivero, I., Avalos, M., Hernández, L.M.

1997 Glycobiology

CITAS

23

DOI

10.1093/glycob/7.4.487

EID

2-s2.0-0342979677

ISSN

0959-6658

BIBTEX

@article{Hernandez1997,title = {Isolation of new nonconditional Saccharomyces cerevisiae mutants defective in asparagine-linked glycosylation},journal = {Glycobiology},year = {1997},volume = {7},number = {4},pages = {487-497},author = {Ma{\~n}as, P. and Olivero, I. and Avalos, M. and Hern{\'a}ndez, L.M.}}

AUTORES DE LA UEX

Luis Miguel Hernández Martín

OTRAS PUBLICACIONES DE INTERÉS

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Genetic Improvement Of Torulaspora Delbrueckii For Wine Fermentation: Eliminating Recessive Growth-Retarding Alleles And Obtaining New Mutants Resistant To So2, Ethanol, And High Co2 Pressure
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Computational Screening Of New Orthogonal Metal-Free Dipolar Cycloadditions Of Mesomeric Betaines
Genetic Improvement Of Torulaspora Delbrueckii For Wine Fermentation: Eliminating Recessive Growth-Retarding Alleles And Obtaining New Mutants Resistant To So2, Ethanol, And High Co2 Pressure
Computational Screening Of New Orthogonal Metal-Free Dipolar Cycloadditions Of Mesomeric Betaines
On The Dual Reactivity Of A Janus-Type Mesoionic Dipole: Experiments And Theoretical Validation
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On The Dual Reactivity Of A Janus-Type Mesoionic Dipole: Experiments And Theoretical Validation
Mechanistic Studies Of 1,3-Dipolar Cycloadditions Of Bicyclic Thioisomünchnones With Alkenes. A Computational Rationale Focused On Donor-Acceptor Interactions
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Prebiotic-Like Condensations Of Cyanamide And Glyoxal: Revisiting Intractable Biotars
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Prebiotic-Like Condensations Of Cyanamide And Glyoxal: Revisiting Intractable Biotars
On The Plausibility Of Pseudosugar Formation In Cometary Ices And Oxygen-Rich Tholins
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Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
Effects Of New Torulaspora Delbrueckii Killer Yeasts On The Must Fermentation Kinetics And Aroma Compounds Of White Table Wine
Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
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Pseudo-Cyclic Structures Of Mono- And Di-Azaderivatives Of Malondialdehydes. Synthesis And Conformational Disentanglement By Computational Analyses
Effects Of New Torulaspora Delbrueckii Killer Yeasts On The Must Fermentation Kinetics And Aroma Compounds Of White Table Wine
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Stepwise Formation Of 1,3-Diazolium-4-Thiolates By Münchnone Cycloadditions: Promising Candidates For Nonlinear Optics
Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures
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Hydrazones From Hydroxy Naphthaldehydes And N-Aminoheterocycles: Structure And Stereodynamics
Identification Of The Mnn3 Gene Of Saccharomyces Cerevisiae
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Identification Of The Mnn3 Gene Of Saccharomyces Cerevisiae
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Schiff Bases From Tris And Formylpyridines: Structure And Mechanistic Rationale Aided By Dft Calculations
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Schiff Bases From Tris And Formylpyridines: Structure And Mechanistic Rationale Aided By Dft Calculations
An Anomeric Effect Drives The Regiospecific Ring-Opening Of 1,3-Oxazolidines Under Acetylating Conditions
Schiff Bases From Tris And Formylpyridines: Structure And Mechanistic Rationale Aided By Dft Calculations
An Anomeric Effect Drives The Regiospecific Ring-Opening Of 1,3-Oxazolidines Under Acetylating Conditions
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Unusual Aryl Migration In A Mesomeric Betaine In The Solid And Liquid State: Mechanistic Insights Into The Snar Reaction
Homochirality And Chemical Evolution: New Vistas And Reflections On Recent Models
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A New Model For Mapping The Peptide Backbone: Predicting Proton Chemical Shifts In Proteins
Homochirality And Chemical Evolution: New Vistas And Reflections On Recent Models
A New Model For Mapping The Peptide Backbone: Predicting Proton Chemical Shifts In Proteins
Schiff Bases From D-Glucosamine And Aliphatic Ketones
A New Model For Mapping The Peptide Backbone: Predicting Proton Chemical Shifts In Proteins
Schiff Bases From D-Glucosamine And Aliphatic Ketones
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Schiff Bases From D-Glucosamine And Aliphatic Ketones
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Thionation Of Mesoionics With Isothiocyanates: Evidence Supporting A Four-Step Domino Process And Ruling Out A [2 + 2] Mechanism
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Thionation Of Mesoionics With Isothiocyanates: Evidence Supporting A Four-Step Domino Process And Ruling Out A [2 + 2] Mechanism
An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine
Thionation Of Mesoionics With Isothiocyanates: Evidence Supporting A Four-Step Domino Process And Ruling Out A [2 + 2] Mechanism
An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine
A Family Of Hydrogels Based On Ureido-Linked Aminopolyol-Derived Amphiphiles And Bolaamphiphiles: Synthesis, Gelation Under Thermal And Sonochemical Stimuli, And Mesomorphic Characterization
An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine
A Family Of Hydrogels Based On Ureido-Linked Aminopolyol-Derived Amphiphiles And Bolaamphiphiles: Synthesis, Gelation Under Thermal And Sonochemical Stimuli, And Mesomorphic Characterization
Stepwise Cycloadditions Of Mesoionic Systems: Thionation Of Thioisomunchnones By Isothiocyanates
A Family Of Hydrogels Based On Ureido-Linked Aminopolyol-Derived Amphiphiles And Bolaamphiphiles: Synthesis, Gelation Under Thermal And Sonochemical Stimuli, And Mesomorphic Characterization
Stepwise Cycloadditions Of Mesoionic Systems: Thionation Of Thioisomunchnones By Isothiocyanates
Chiral N-Acyloxazolidines: Synthesis, Structure, And Mechanistic Insights
Stepwise Cycloadditions Of Mesoionic Systems: Thionation Of Thioisomunchnones By Isothiocyanates
Chiral N-Acyloxazolidines: Synthesis, Structure, And Mechanistic Insights
Genome-Wide Expression Profile Of The Mnn2δ Mutant Of Saccharomyces Cerevisiae
Chiral N-Acyloxazolidines: Synthesis, Structure, And Mechanistic Insights
Genome-Wide Expression Profile Of The Mnn2δ Mutant Of Saccharomyces Cerevisiae
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Genome-Wide Expression Profile Of The Mnn2δ Mutant Of Saccharomyces Cerevisiae
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
Greener Media In Chemical Synthesis And Processing
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
Greener Media In Chemical Synthesis And Processing
A One-Pot Domino Reaction In Constructing Isoorotate Bases And Their Nucleosides
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A One-Pot Domino Reaction In Constructing Isoorotate Bases And Their Nucleosides
Synthesis Of Sugar Isocyanates And Their Application To The Formation Of Ureido-Linked Disaccharides
A One-Pot Domino Reaction In Constructing Isoorotate Bases And Their Nucleosides
Synthesis Of Sugar Isocyanates And Their Application To The Formation Of Ureido-Linked Disaccharides
A Genome-Wide Screen For Saccharomyces Cerevisiae Nonessential Genes Involved In Mannosyl Phosphate Transfer To Mannoprotein-Linked Oligosaccharides
Synthesis Of Sugar Isocyanates And Their Application To The Formation Of Ureido-Linked Disaccharides
A Genome-Wide Screen For Saccharomyces Cerevisiae Nonessential Genes Involved In Mannosyl Phosphate Transfer To Mannoprotein-Linked Oligosaccharides
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
A Genome-Wide Screen For Saccharomyces Cerevisiae Nonessential Genes Involved In Mannosyl Phosphate Transfer To Mannoprotein-Linked Oligosaccharides
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
Exploiting Synthetic Chemistry With Mesoionic Rings: Improvements Achieved With Thioisomünchnones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
Exploiting Synthetic Chemistry With Mesoionic Rings: Improvements Achieved With Thioisomünchnones
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Exploiting Synthetic Chemistry With Mesoionic Rings: Improvements Achieved With Thioisomünchnones
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Identification Of Low-Dye-Binding (Ldb) Mutants Of Saccharomyces Cerevisiae
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Identification Of Low-Dye-Binding (Ldb) Mutants Of Saccharomyces Cerevisiae
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Identification Of Low-Dye-Binding (Ldb) Mutants Of Saccharomyces Cerevisiae
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Symmetry Breaking: An Epistemological Note
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Symmetry Breaking: An Epistemological Note
Symmetry Breaking By Spontaneous Crystallization - Is It The Most Plausible Source Of Terrestrial Handedness We Have Long Been Looking For? - A Reappraisal
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The Ldb1 Mutant Of Saccharomyces Cerevisiae Is Defective In Pmr1p, The Yeast Secretory Pathway/golgi Ca2+/mn2+-Atpase
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
The Ldb1 Mutant Of Saccharomyces Cerevisiae Is Defective In Pmr1p, The Yeast Secretory Pathway/golgi Ca2+/mn2+-Atpase
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism
1,3-Dipolar Cycloaddition Of 2-Dialkylaminothioisomünchnones With Aliphatic Aldehydes: Synthesis Of Β-Lactams And Thiiranes, Structure Elucidation, And Rationale For Chemoselective Fragmentation Of Cycloadducts
Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism
1,3-Dipolar Cycloaddition Of 2-Dialkylaminothioisomünchnones With Aliphatic Aldehydes: Synthesis Of Β-Lactams And Thiiranes, Structure Elucidation, And Rationale For Chemoselective Fragmentation Of Cycloadducts
Conformation Of Secondary Amides. A Predictive Algorithm That Correlates Dft-Calculated Structures And Experimental Proton Chemical Shifts
1,3-Dipolar Cycloaddition Of 2-Dialkylaminothioisomünchnones With Aliphatic Aldehydes: Synthesis Of Β-Lactams And Thiiranes, Structure Elucidation, And Rationale For Chemoselective Fragmentation Of Cycloadducts
Conformation Of Secondary Amides. A Predictive Algorithm That Correlates Dft-Calculated Structures And Experimental Proton Chemical Shifts
What Does Elementary Chirality Have To Do With Neutrinos?
Conformation Of Secondary Amides. A Predictive Algorithm That Correlates Dft-Calculated Structures And Experimental Proton Chemical Shifts
What Does Elementary Chirality Have To Do With Neutrinos?
Experimental And Theoretical Insights Regarding The Cycloaddition Reaction Of Carbohydrate-Based 1,2-Diaza-1,3-Butadienes And Acrylonitrile. A Model Case For The Behavior Of Chiral Azoalkenes And Unsymmetric Olefins
What Does Elementary Chirality Have To Do With Neutrinos?
Experimental And Theoretical Insights Regarding The Cycloaddition Reaction Of Carbohydrate-Based 1,2-Diaza-1,3-Butadienes And Acrylonitrile. A Model Case For The Behavior Of Chiral Azoalkenes And Unsymmetric Olefins
Novel Acid-Catalyzed Rearrangement Of Tetrahydro-1,2,3,4-Tetrazines: Unexpected Formation Of Glycosazones
Experimental And Theoretical Insights Regarding The Cycloaddition Reaction Of Carbohydrate-Based 1,2-Diaza-1,3-Butadienes And Acrylonitrile. A Model Case For The Behavior Of Chiral Azoalkenes And Unsymmetric Olefins
Novel Acid-Catalyzed Rearrangement Of Tetrahydro-1,2,3,4-Tetrazines: Unexpected Formation Of Glycosazones
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Novel Acid-Catalyzed Rearrangement Of Tetrahydro-1,2,3,4-Tetrazines: Unexpected Formation Of Glycosazones
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Can We Predict The Conformational Preference Of Amides?
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Can We Predict The Conformational Preference Of Amides?
Carbohydrates As Chiral Controllers: Synthesis Of Dihydrothieno[2,3-C]furanones
Can We Predict The Conformational Preference Of Amides?
Carbohydrates As Chiral Controllers: Synthesis Of Dihydrothieno[2,3-C]furanones
A Cycloaddition Strategy For The Synthesis Of Thiirane-Containing Glycomimetics
Carbohydrates As Chiral Controllers: Synthesis Of Dihydrothieno[2,3-C]furanones
A Cycloaddition Strategy For The Synthesis Of Thiirane-Containing Glycomimetics
Synergic Effect Of Vicinal Stereocenters In [3 + 2] Cycloadditions Of Carbohydrate Azadipolarophiles And Mesoionic Dipoles: Origin Of Diastereofacial Selectivity
A Cycloaddition Strategy For The Synthesis Of Thiirane-Containing Glycomimetics
Synergic Effect Of Vicinal Stereocenters In [3 + 2] Cycloadditions Of Carbohydrate Azadipolarophiles And Mesoionic Dipoles: Origin Of Diastereofacial Selectivity
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
Synergic Effect Of Vicinal Stereocenters In [3 + 2] Cycloadditions Of Carbohydrate Azadipolarophiles And Mesoionic Dipoles: Origin Of Diastereofacial Selectivity
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
Conjugate Additions Of Heteronucleophiles To Enones And Alkynoates. A 'benign By Design' Functionalization Of Heteroaromatics
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
Conjugate Additions Of Heteronucleophiles To Enones And Alkynoates. A 'benign By Design' Functionalization Of Heteroaromatics
Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone-Alkene Cycloaddition Reaction
Conjugate Additions Of Heteronucleophiles To Enones And Alkynoates. A 'benign By Design' Functionalization Of Heteroaromatics
Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone-Alkene Cycloaddition Reaction
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone-Alkene Cycloaddition Reaction
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
The First Density Functional Study On The [4 + 2]-Cycloaddition Reactions Of 1,2-Diaza-1,3-Butadiene With Alkenes
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
The First Density Functional Study On The [4 + 2]-Cycloaddition Reactions Of 1,2-Diaza-1,3-Butadiene With Alkenes
Computational Studies On The Bf3-Catalyzed Cycloaddition Of Furan With Methyl Vinyl Ketone: A New Look At Lewis Acid Catalysis
The First Density Functional Study On The [4 + 2]-Cycloaddition Reactions Of 1,2-Diaza-1,3-Butadiene With Alkenes
Computational Studies On The Bf3-Catalyzed Cycloaddition Of Furan With Methyl Vinyl Ketone: A New Look At Lewis Acid Catalysis
Diastereoselective Cycloadditions Of 1,3-Thiazolium-4-Olates With Chiral 1,2-Diaza-1,3-Butadienes
Computational Studies On The Bf3-Catalyzed Cycloaddition Of Furan With Methyl Vinyl Ketone: A New Look At Lewis Acid Catalysis
Diastereoselective Cycloadditions Of 1,3-Thiazolium-4-Olates With Chiral 1,2-Diaza-1,3-Butadienes
From Parity To Chirality: Chemical Implications Revisited
Diastereoselective Cycloadditions Of 1,3-Thiazolium-4-Olates With Chiral 1,2-Diaza-1,3-Butadienes
From Parity To Chirality: Chemical Implications Revisited
Chiral Autocatalysis: Where Stereochemistry Meets The Origin Of Life
From Parity To Chirality: Chemical Implications Revisited
Chiral Autocatalysis: Where Stereochemistry Meets The Origin Of Life
Sonochemical Cycloadditions Of O-Quinones. The Search For A Cation Radical Pathway
Chiral Autocatalysis: Where Stereochemistry Meets The Origin Of Life
Sonochemical Cycloadditions Of O-Quinones. The Search For A Cation Radical Pathway
Optically Active Sugar Thioamides From Δ-Gluconolactone
Sonochemical Cycloadditions Of O-Quinones. The Search For A Cation Radical Pathway
Optically Active Sugar Thioamides From Δ-Gluconolactone
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Optically Active Sugar Thioamides From Δ-Gluconolactone
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Understanding Diastereofacial Selection In Carbohydrate-Based Domino Cycloadditions: Semiempirical And Dft Calculations
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Understanding Diastereofacial Selection In Carbohydrate-Based Domino Cycloadditions: Semiempirical And Dft Calculations
The Mnn2 Mutant Of Saccharomyces Cerevisiae Is Affected In Phosphorylation Of N-Linked Oligosaccharides
Understanding Diastereofacial Selection In Carbohydrate-Based Domino Cycloadditions: Semiempirical And Dft Calculations
The Mnn2 Mutant Of Saccharomyces Cerevisiae Is Affected In Phosphorylation Of N-Linked Oligosaccharides
Preparation Of Riboflavin 4',5'-Cyclic Phosphate By Incubation Of Flavin-Adenine Dinucleotide With Mn2+ In The Absence Of Riboflavin 5'- Phosphate Cyclase
The Mnn2 Mutant Of Saccharomyces Cerevisiae Is Affected In Phosphorylation Of N-Linked Oligosaccharides
Preparation Of Riboflavin 4',5'-Cyclic Phosphate By Incubation Of Flavin-Adenine Dinucleotide With Mn2+ In The Absence Of Riboflavin 5'- Phosphate Cyclase
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Preparation Of Riboflavin 4',5'-Cyclic Phosphate By Incubation Of Flavin-Adenine Dinucleotide With Mn2+ In The Absence Of Riboflavin 5'- Phosphate Cyclase
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Hetero-Diels-Alder Reactions Of Homochiral 1,2-Diaza-1,3-Butadienes With Diethyl Azodicarboxylate Under Microwave Irradiation. Theoretical Rationale Of The Stereochemical Outcome
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Hetero-Diels-Alder Reactions Of Homochiral 1,2-Diaza-1,3-Butadienes With Diethyl Azodicarboxylate Under Microwave Irradiation. Theoretical Rationale Of The Stereochemical Outcome
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Hetero-Diels-Alder Reactions Of Homochiral 1,2-Diaza-1,3-Butadienes With Diethyl Azodicarboxylate Under Microwave Irradiation. Theoretical Rationale Of The Stereochemical Outcome
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Diastereoselective Cycloadditions Of Nitroalkenes As An Approach To The Assembly Of Bicyclic Nitrogen Heterocycles
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Diastereoselective Cycloadditions Of Nitroalkenes As An Approach To The Assembly Of Bicyclic Nitrogen Heterocycles
Synthetic Variations Based On Low-Valent Chromium: New Developments
Diastereoselective Cycloadditions Of Nitroalkenes As An Approach To The Assembly Of Bicyclic Nitrogen Heterocycles
Synthetic Variations Based On Low-Valent Chromium: New Developments
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Synthetic Variations Based On Low-Valent Chromium: New Developments
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Clay-Catalyzed Solventless Addition Reactions Of Furan With Α,β- Unsaturated Carbonyl Compounds
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Clay-Catalyzed Solventless Addition Reactions Of Furan With Α,β- Unsaturated Carbonyl Compounds
Cycloadditions With Clays And Alumina Without Solvents
Clay-Catalyzed Solventless Addition Reactions Of Furan With Α,β- Unsaturated Carbonyl Compounds
Cycloadditions With Clays And Alumina Without Solvents
The Structure Of Glycosyl Amides: A Combined Study By Nmr Spectroscopy, X-Ray Crystallography, And Computational Chemistry
Cycloadditions With Clays And Alumina Without Solvents
The Structure Of Glycosyl Amides: A Combined Study By Nmr Spectroscopy, X-Ray Crystallography, And Computational Chemistry
Absolute Asymmetric Synthesis Under Physical Fields: Facts And Fictions
The Structure Of Glycosyl Amides: A Combined Study By Nmr Spectroscopy, X-Ray Crystallography, And Computational Chemistry
Absolute Asymmetric Synthesis Under Physical Fields: Facts And Fictions
Asymmetric Tandem Reactions Based On Nitroalkenes: A One-Pot Construction Of Functionalized Chiral Bicycles By A Three-Component Reaction
Absolute Asymmetric Synthesis Under Physical Fields: Facts And Fictions
Asymmetric Tandem Reactions Based On Nitroalkenes: A One-Pot Construction Of Functionalized Chiral Bicycles By A Three-Component Reaction
Proteolytic Processing Of A Secreted Glycoprotein And O-Glycosylation Of Mannoproteins Are Affected In The N-Glycosylation Mutant Saccharomyces Cerevisiae Ldb1
Asymmetric Tandem Reactions Based On Nitroalkenes: A One-Pot Construction Of Functionalized Chiral Bicycles By A Three-Component Reaction
Proteolytic Processing Of A Secreted Glycoprotein And O-Glycosylation Of Mannoproteins Are Affected In The N-Glycosylation Mutant Saccharomyces Cerevisiae Ldb1
Enzymic Formation Of Riboflavin 4′,5′-Cyclic Phosphate From Fad: Evidence For A Specific Low-Km Fmn Cyclase In Rat Liver
Proteolytic Processing Of A Secreted Glycoprotein And O-Glycosylation Of Mannoproteins Are Affected In The N-Glycosylation Mutant Saccharomyces Cerevisiae Ldb1
Enzymic Formation Of Riboflavin 4′,5′-Cyclic Phosphate From Fad: Evidence For A Specific Low-Km Fmn Cyclase In Rat Liver
Glycine-Enhanced Inhibition Of Rat Liver Nucleotide Pyrophosphatase/phosphodiesterase-I By Edta: A Full Account Of The Reported Inhibition By Commercial Preparations Of Acidic Fibroblast Growth Factor (Fgf-1)
Enzymic Formation Of Riboflavin 4′,5′-Cyclic Phosphate From Fad: Evidence For A Specific Low-Km Fmn Cyclase In Rat Liver
Glycine-Enhanced Inhibition Of Rat Liver Nucleotide Pyrophosphatase/phosphodiesterase-I By Edta: A Full Account Of The Reported Inhibition By Commercial Preparations Of Acidic Fibroblast Growth Factor (Fgf-1)
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Glycine-Enhanced Inhibition Of Rat Liver Nucleotide Pyrophosphatase/phosphodiesterase-I By Edta: A Full Account Of The Reported Inhibition By Commercial Preparations Of Acidic Fibroblast Growth Factor (Fgf-1)
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Nonlinear Stereochemical Effects In Asymmetric Reactions
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Nonlinear Stereochemical Effects In Asymmetric Reactions
Identification Of Rat Liver Glucose-3-Phosphatase As An Inositol Monophosphatase Inhibited By Lithium
Nonlinear Stereochemical Effects In Asymmetric Reactions
Identification Of Rat Liver Glucose-3-Phosphatase As An Inositol Monophosphatase Inhibited By Lithium
Isolation Of New Nonconditional Saccharomyces Cerevisiae Mutants Defective In Asparagine-Linked Glycosylation
Identification Of Rat Liver Glucose-3-Phosphatase As An Inositol Monophosphatase Inhibited By Lithium
Isolation Of New Nonconditional Saccharomyces Cerevisiae Mutants Defective In Asparagine-Linked Glycosylation
Nmr Studies And Semiempirical Calculations On The Structure Of Glycoamidines
Isolation Of New Nonconditional Saccharomyces Cerevisiae Mutants Defective In Asparagine-Linked Glycosylation
Nmr Studies And Semiempirical Calculations On The Structure Of Glycoamidines
Cycloaddition Chemistry Of 1,3-Thiazolium-4-Olate Systems. Reaction With Nitroalkenes And Interpretation Of Results Using Pm3 Calculations
Nmr Studies And Semiempirical Calculations On The Structure Of Glycoamidines
Cycloaddition Chemistry Of 1,3-Thiazolium-4-Olate Systems. Reaction With Nitroalkenes And Interpretation Of Results Using Pm3 Calculations
Substrate-Controlled Stereodifferentiation Of Tandem [4 + 2]/[3 + 2] Cycloadditions By A Vicinal Carbohydrate-Based Template
Cycloaddition Chemistry Of 1,3-Thiazolium-4-Olate Systems. Reaction With Nitroalkenes And Interpretation Of Results Using Pm3 Calculations
Substrate-Controlled Stereodifferentiation Of Tandem [4 + 2]/[3 + 2] Cycloadditions By A Vicinal Carbohydrate-Based Template
A Simple, Cip-Based Notation System For The Unambiguous Specification Of Asymmetric Reactions
Substrate-Controlled Stereodifferentiation Of Tandem [4 + 2]/[3 + 2] Cycloadditions By A Vicinal Carbohydrate-Based Template
A Simple, Cip-Based Notation System For The Unambiguous Specification Of Asymmetric Reactions
Münchnone-Alkene Cycloadditions: Deviations From The Fmo Theory. Theoretical Studies In The Search Of The Transition State
A Simple, Cip-Based Notation System For The Unambiguous Specification Of Asymmetric Reactions
Münchnone-Alkene Cycloadditions: Deviations From The Fmo Theory. Theoretical Studies In The Search Of The Transition State
Synthesis Of Glycoamidines Using A Mercury-Promoted Reaction
Münchnone-Alkene Cycloadditions: Deviations From The Fmo Theory. Theoretical Studies In The Search Of The Transition State
Synthesis Of Glycoamidines Using A Mercury-Promoted Reaction
A Facile And Expeditious Entry To Acyclic Carbohydrate-Derived 1,2-Diazabutadienes
Synthesis Of Glycoamidines Using A Mercury-Promoted Reaction
A Facile And Expeditious Entry To Acyclic Carbohydrate-Derived 1,2-Diazabutadienes
A Novel Highly Diastereoselective Synthesis Of Chiral Dihydrothiophenes From Mesoionic Compounds
A Facile And Expeditious Entry To Acyclic Carbohydrate-Derived 1,2-Diazabutadienes
A Novel Highly Diastereoselective Synthesis Of Chiral Dihydrothiophenes From Mesoionic Compounds
Glycosylation Of Yeast Exoglucanase Sequons In Alg Mutants Deficient In The Glucosylation Steps Of The Lipid-Linked Oligosaccharide. Presence Of Glucotriose Unit In Dol-Pp-Glcnac2man9glc3 Influences Both Glycosylation Efficiency And Selection Of N-Linked Sites
A Novel Highly Diastereoselective Synthesis Of Chiral Dihydrothiophenes From Mesoionic Compounds
Glycosylation Of Yeast Exoglucanase Sequons In Alg Mutants Deficient In The Glucosylation Steps Of The Lipid-Linked Oligosaccharide. Presence Of Glucotriose Unit In Dol-Pp-Glcnac2man9glc3 Influences Both Glycosylation Efficiency And Selection Of N-Linked Sites
Selective Elongation Of The Oligosaccharide Attached To The Second Potential Glycosylation Site Of Yeast Exoglucanase: Effects On The Activity And Properties Of The Enzyme
Glycosylation Of Yeast Exoglucanase Sequons In Alg Mutants Deficient In The Glucosylation Steps Of The Lipid-Linked Oligosaccharide. Presence Of Glucotriose Unit In Dol-Pp-Glcnac2man9glc3 Influences Both Glycosylation Efficiency And Selection Of N-Linked Sites
Selective Elongation Of The Oligosaccharide Attached To The Second Potential Glycosylation Site Of Yeast Exoglucanase: Effects On The Activity And Properties Of The Enzyme
Condensation Of 2-Amino-2-Deoxysugars With Isothiocyanates. Synthesis Of Cis-1,2-Fused Glycopyrano Heterocycles.
Selective Elongation Of The Oligosaccharide Attached To The Second Potential Glycosylation Site Of Yeast Exoglucanase: Effects On The Activity And Properties Of The Enzyme
Condensation Of 2-Amino-2-Deoxysugars With Isothiocyanates. Synthesis Of Cis-1,2-Fused Glycopyrano Heterocycles.
Reaction Of Thioamides With Silver Carboxylates In Aprotic Media. A Nucleophilic Approach To The Synthesis Of Imides, Amides, And Nitriles
Condensation Of 2-Amino-2-Deoxysugars With Isothiocyanates. Synthesis Of Cis-1,2-Fused Glycopyrano Heterocycles.
Reaction Of Thioamides With Silver Carboxylates In Aprotic Media. A Nucleophilic Approach To The Synthesis Of Imides, Amides, And Nitriles
Reduced Efficiency In The Glycosylation Of The First Sequon Of Saccharomyces Cerevisiae Exoglucanase Leads To The Synthesis And Secretion Of A New Glycoform Of The Molecule
Reaction Of Thioamides With Silver Carboxylates In Aprotic Media. A Nucleophilic Approach To The Synthesis Of Imides, Amides, And Nitriles
Reduced Efficiency In The Glycosylation Of The First Sequon Of Saccharomyces Cerevisiae Exoglucanase Leads To The Synthesis And Secretion Of A New Glycoform Of The Molecule
Structure Of Adducts Of 2-Arylaminothiazolines With Isocyanates And Isothiocyanates
Reduced Efficiency In The Glycosylation Of The First Sequon Of Saccharomyces Cerevisiae Exoglucanase Leads To The Synthesis And Secretion Of A New Glycoform Of The Molecule
Structure Of Adducts Of 2-Arylaminothiazolines With Isocyanates And Isothiocyanates
On The Mechanism Of Formation Of Glycofurano[2,1-D]-Imidazolidin-2-Ones. Reaction Of 2-Amino-2-Deoxyheptopyranoses With Isocyanates.
Structure Of Adducts Of 2-Arylaminothiazolines With Isocyanates And Isothiocyanates
On The Mechanism Of Formation Of Glycofurano[2,1-D]-Imidazolidin-2-Ones. Reaction Of 2-Amino-2-Deoxyheptopyranoses With Isocyanates.
The Reaction Of 2-Amino-2-Deoxyhexopyranoses With Isocyanates. Synthesis Of Ureas And Their Transformation Into Heterocyclic Derivatives.
On The Mechanism Of Formation Of Glycofurano[2,1-D]-Imidazolidin-2-Ones. Reaction Of 2-Amino-2-Deoxyheptopyranoses With Isocyanates.
The Reaction Of 2-Amino-2-Deoxyhexopyranoses With Isocyanates. Synthesis Of Ureas And Their Transformation Into Heterocyclic Derivatives.
A Novel Regio- And Highly Stereoselective Anomeric Deacetylation Of 2-Aminosugar Derivatives
The Reaction Of 2-Amino-2-Deoxyhexopyranoses With Isocyanates. Synthesis Of Ureas And Their Transformation Into Heterocyclic Derivatives.
A Novel Regio- And Highly Stereoselective Anomeric Deacetylation Of 2-Aminosugar Derivatives
Diastereoselective Synthesis Of Chiral Thiiranes By 1,3-Dipolar Cycloaddition Of Imidazo[2,1-B]thiazolium-4-Olate Systems With Aromatic Aldehydes
A Novel Regio- And Highly Stereoselective Anomeric Deacetylation Of 2-Aminosugar Derivatives
Diastereoselective Synthesis Of Chiral Thiiranes By 1,3-Dipolar Cycloaddition Of Imidazo[2,1-B]thiazolium-4-Olate Systems With Aromatic Aldehydes
Alcohol Esterification Reactions And Mechanisms Of Snake Venom 5′‐nucleotide Phosphodiesterase
Diastereoselective Synthesis Of Chiral Thiiranes By 1,3-Dipolar Cycloaddition Of Imidazo[2,1-B]thiazolium-4-Olate Systems With Aromatic Aldehydes
Alcohol Esterification Reactions And Mechanisms Of Snake Venom 5′‐nucleotide Phosphodiesterase
Oligosaccharide Structures Of The Major Exoglucanase Secreted By Saccharomyces Cerevisiae
Alcohol Esterification Reactions And Mechanisms Of Snake Venom 5′‐nucleotide Phosphodiesterase
Oligosaccharide Structures Of The Major Exoglucanase Secreted By Saccharomyces Cerevisiae
Haloalkyl Isothiocyanates, Useful And Versatile Reagents In Heterocyclic Chemistry
Oligosaccharide Structures Of The Major Exoglucanase Secreted By Saccharomyces Cerevisiae
Haloalkyl Isothiocyanates, Useful And Versatile Reagents In Heterocyclic Chemistry
Nmr Studies Of Sugar Amides And Thioamides
Haloalkyl Isothiocyanates, Useful And Versatile Reagents In Heterocyclic Chemistry
Nmr Studies Of Sugar Amides And Thioamides
A New Synthesis Of 6-Oxopyrimidinium-4-Olates. Theoretical Study Of The Regioselective Cycloaddition Of Arylisocyanates With A 1,3-Thiazolium-4-Olate System
Nmr Studies Of Sugar Amides And Thioamides
A New Synthesis Of 6-Oxopyrimidinium-4-Olates. Theoretical Study Of The Regioselective Cycloaddition Of Arylisocyanates With A 1,3-Thiazolium-4-Olate System
Diastereofacial Selectivity In Diels-Alder Reactions Of Chiral 1,2-Diaza-1,3-Butadienes From Carbohydrates
A New Synthesis Of 6-Oxopyrimidinium-4-Olates. Theoretical Study Of The Regioselective Cycloaddition Of Arylisocyanates With A 1,3-Thiazolium-4-Olate System
Diastereofacial Selectivity In Diels-Alder Reactions Of Chiral 1,2-Diaza-1,3-Butadienes From Carbohydrates
Synthesis And Reactivity Toward Acetylenic Dipolarophiles Of Imidazo[2,1-B]thiazolium-3-Olate Systems
Diastereofacial Selectivity In Diels-Alder Reactions Of Chiral 1,2-Diaza-1,3-Butadienes From Carbohydrates
Synthesis And Reactivity Toward Acetylenic Dipolarophiles Of Imidazo[2,1-B]thiazolium-3-Olate Systems
Methanol Esterification Reactions Catalyzed By Snake Venom And Bovine Intestinal 5′‐nucleotide Phosphodiesterases: Formation Of Nucleoside 5′‐monophosphate Methyl Esters From Guanosine 5′‐triphosphate And Other Nucleoside 5′‐polyphosphates
Synthesis And Reactivity Toward Acetylenic Dipolarophiles Of Imidazo[2,1-B]thiazolium-3-Olate Systems
Methanol Esterification Reactions Catalyzed By Snake Venom And Bovine Intestinal 5′‐nucleotide Phosphodiesterases: Formation Of Nucleoside 5′‐monophosphate Methyl Esters From Guanosine 5′‐triphosphate And Other Nucleoside 5′‐polyphosphates
Two Glycosylation Patterns For A Single Protein (Exoglucanase) In Saccharomyces Cerevisiae
Methanol Esterification Reactions Catalyzed By Snake Venom And Bovine Intestinal 5′‐nucleotide Phosphodiesterases: Formation Of Nucleoside 5′‐monophosphate Methyl Esters From Guanosine 5′‐triphosphate And Other Nucleoside 5′‐polyphosphates
Two Glycosylation Patterns For A Single Protein (Exoglucanase) In Saccharomyces Cerevisiae
Separation Of Yeast Asparagine-Linked Oligosaccharides By High-Performance Anion-Exchange Chromatography
Two Glycosylation Patterns For A Single Protein (Exoglucanase) In Saccharomyces Cerevisiae
Separation Of Yeast Asparagine-Linked Oligosaccharides By High-Performance Anion-Exchange Chromatography
Revision Of The Oligosaccharide Structures Of Yeast Carboxypeptidase Y
Separation Of Yeast Asparagine-Linked Oligosaccharides By High-Performance Anion-Exchange Chromatography
Revision Of The Oligosaccharide Structures Of Yeast Carboxypeptidase Y
Localization Of Αl→3-Linked Mannoses In The N-Linked Oligosaccharides Of Saccharomyces Cerevisiae Mnn Mutants
Revision Of The Oligosaccharide Structures Of Yeast Carboxypeptidase Y
Localization Of Αl→3-Linked Mannoses In The N-Linked Oligosaccharides Of Saccharomyces Cerevisiae Mnn Mutants
Synthesis Of Sugar N-(2-Thiazolin-2-Yl)thioureas
Localization Of Αl→3-Linked Mannoses In The N-Linked Oligosaccharides Of Saccharomyces Cerevisiae Mnn Mutants
Synthesis Of Sugar N-(2-Thiazolin-2-Yl)thioureas
Synthesis Of 2-Alkyl(Aryl)amino-(3,4,6-Tri-O-Acetyl-1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Oxazolines And Ethyl 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-Β-D-Glucopyranosides From Acetylated 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-D-Glucopyranoses
Synthesis Of Sugar N-(2-Thiazolin-2-Yl)thioureas
Synthesis Of 2-Alkyl(Aryl)amino-(3,4,6-Tri-O-Acetyl-1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Oxazolines And Ethyl 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-Β-D-Glucopyranosides From Acetylated 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-D-Glucopyranoses
Synthesis Of Acylated Thioureylenedisaccharides
Synthesis Of 2-Alkyl(Aryl)amino-(3,4,6-Tri-O-Acetyl-1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Oxazolines And Ethyl 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-Β-D-Glucopyranosides From Acetylated 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-D-Glucopyranoses
Synthesis Of Acylated Thioureylenedisaccharides
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine. Synthesis And Structure Of N-Nucleoside Analogues
Synthesis Of Acylated Thioureylenedisaccharides
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine. Synthesis And Structure Of N-Nucleoside Analogues
Synthesis Of N,n′-Bis(Aryl)-N-(2-Thiazolin-2-Yl)thioureas
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine. Synthesis And Structure Of N-Nucleoside Analogues
Synthesis Of N,n′-Bis(Aryl)-N-(2-Thiazolin-2-Yl)thioureas
Reduction Of Isothiocyanates To Thioformamides With Tri-N-Butyltin Hydride
Synthesis Of N,n′-Bis(Aryl)-N-(2-Thiazolin-2-Yl)thioureas
Reduction Of Isothiocyanates To Thioformamides With Tri-N-Butyltin Hydride
Structure Of The Phosphorylated N-Linked Oligosaccharides From The Mnn9 And Mnn10 Mutants Of Saccharomyces Cerevisiae
Reduction Of Isothiocyanates To Thioformamides With Tri-N-Butyltin Hydride
Structure Of The Phosphorylated N-Linked Oligosaccharides From The Mnn9 And Mnn10 Mutants Of Saccharomyces Cerevisiae
A New Saccharomyces Cerevisiae Mnn Mutant-N-Linked Oligosaccharide Structure
Structure Of The Phosphorylated N-Linked Oligosaccharides From The Mnn9 And Mnn10 Mutants Of Saccharomyces Cerevisiae
A New Saccharomyces Cerevisiae Mnn Mutant-N-Linked Oligosaccharide Structure
Synthesis Of Glycofurano[2,1-D]imidazolidin-2-Ones
A New Saccharomyces Cerevisiae Mnn Mutant-N-Linked Oligosaccharide Structure
Synthesis Of Glycofurano[2,1-D]imidazolidin-2-Ones
An Efficient And Regioselective Synthesis Of Acyclic C-Nucleosides From Mesoionic Compounds
Synthesis Of Glycofurano[2,1-D]imidazolidin-2-Ones
An Efficient And Regioselective Synthesis Of Acyclic C-Nucleosides From Mesoionic Compounds
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine
An Efficient And Regioselective Synthesis Of Acyclic C-Nucleosides From Mesoionic Compounds
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine
A Similar Protein Portion For Two Exoglucanases Secreted By Saccharomyces Cerevisiae
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine
A Similar Protein Portion For Two Exoglucanases Secreted By Saccharomyces Cerevisiae
Two Ionic Forms Of Exoglucanase In Yeast Secretory Mutants
A Similar Protein Portion For Two Exoglucanases Secreted By Saccharomyces Cerevisiae
Two Ionic Forms Of Exoglucanase In Yeast Secretory Mutants
Síntesis De Hidrobromuros De Glucopirano [2,1-D]-2-Tiazolinas
Two Ionic Forms Of Exoglucanase In Yeast Secretory Mutants
Síntesis De Hidrobromuros De Glucopirano [2,1-D]-2-Tiazolinas
Acylation Of Glycofurano[2,1-D]imidazolidine-2-Thiones: A Structural Revision
Síntesis De Hidrobromuros De Glucopirano [2,1-D]-2-Tiazolinas
Acylation Of Glycofurano[2,1-D]imidazolidine-2-Thiones: A Structural Revision
Facile Preparation Of C-Glycosylbarbiturates And C-Glycosylbarbituric Acids
Acylation Of Glycofurano[2,1-D]imidazolidine-2-Thiones: A Structural Revision
Facile Preparation Of C-Glycosylbarbiturates And C-Glycosylbarbituric Acids
Synthesis Of 1,3,4,6-Tetra-O-Acetyl-2-[3-Alkyl-(Aryl)-Thioreido]-2-Deoxy-Α-D-Glucopyranoses And Their Transformation Into 2-Alkyl(Aryl)amino-(1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Thiazolines
Facile Preparation Of C-Glycosylbarbiturates And C-Glycosylbarbituric Acids
Synthesis Of 1,3,4,6-Tetra-O-Acetyl-2-[3-Alkyl-(Aryl)-Thioreido]-2-Deoxy-Α-D-Glucopyranoses And Their Transformation Into 2-Alkyl(Aryl)amino-(1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Thiazolines
Accumulation And Secretion Of Exoglucanase Activity In Yeast Secretory Mutants
Synthesis Of 1,3,4,6-Tetra-O-Acetyl-2-[3-Alkyl-(Aryl)-Thioreido]-2-Deoxy-Α-D-Glucopyranoses And Their Transformation Into 2-Alkyl(Aryl)amino-(1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Thiazolines
Accumulation And Secretion Of Exoglucanase Activity In Yeast Secretory Mutants
Accumulation Of Exoglucanase Activity In Yeast Secretory Mutants Blocked At The Endoplasmic Reticulum Level
Accumulation And Secretion Of Exoglucanase Activity In Yeast Secretory Mutants
Accumulation Of Exoglucanase Activity In Yeast Secretory Mutants Blocked At The Endoplasmic Reticulum Level
3-Alquil-1-Aril(Glicoheptofurano)imidazolidina-2-Tionas Derivadas De Nuevas 2-(Alquilamino)-2-Desoxi-Heptosas De Configuración D-Glicero-L-Gluco, D-Glicero-L-Mano, D-Glicero-D-Gulo Y D-Glicero-D-Ido
Accumulation Of Exoglucanase Activity In Yeast Secretory Mutants Blocked At The Endoplasmic Reticulum Level
3-Alquil-1-Aril(Glicoheptofurano)imidazolidina-2-Tionas Derivadas De Nuevas 2-(Alquilamino)-2-Desoxi-Heptosas De Configuración D-Glicero-L-Gluco, D-Glicero-L-Mano, D-Glicero-D-Gulo Y D-Glicero-D-Ido
New Acyclic-Sugar C-Nucleoside Analogs. Synthesis Of 2-(Alditol-1-Yl)-1-Alkyl-4,5,6,7-Tetrahydroindol-4-Ones
3-Alquil-1-Aril(Glicoheptofurano)imidazolidina-2-Tionas Derivadas De Nuevas 2-(Alquilamino)-2-Desoxi-Heptosas De Configuración D-Glicero-L-Gluco, D-Glicero-L-Mano, D-Glicero-D-Gulo Y D-Glicero-D-Ido
New Acyclic-Sugar C-Nucleoside Analogs. Synthesis Of 2-(Alditol-1-Yl)-1-Alkyl-4,5,6,7-Tetrahydroindol-4-Ones
Regulation Of Β-Exoglucanase Activity Production By Saccharomyces Cerevisiae In Batch And Continuous Culture
New Acyclic-Sugar C-Nucleoside Analogs. Synthesis Of 2-(Alditol-1-Yl)-1-Alkyl-4,5,6,7-Tetrahydroindol-4-Ones
Regulation Of Β-Exoglucanase Activity Production By Saccharomyces Cerevisiae In Batch And Continuous Culture
Tioureas Derivadas De Carbohidratos. V. Isotiocianato Y Tioureas Derivadas De La 2-Amino-2-Desoxi-D-Glicero-Α-L-Gluco-Heptopiranosa
Regulation Of Β-Exoglucanase Activity Production By Saccharomyces Cerevisiae In Batch And Continuous Culture
Tioureas Derivadas De Carbohidratos. V. Isotiocianato Y Tioureas Derivadas De La 2-Amino-2-Desoxi-D-Glicero-Α-L-Gluco-Heptopiranosa
Acyclic-Sugar Pyrrole C-Nucleoside-Analogs Derived From 2-(Alkylamino)-2-Deoxyaldoses
Tioureas Derivadas De Carbohidratos. V. Isotiocianato Y Tioureas Derivadas De La 2-Amino-2-Desoxi-D-Glicero-Α-L-Gluco-Heptopiranosa
Acyclic-Sugar Pyrrole C-Nucleoside-Analogs Derived From 2-(Alkylamino)-2-Deoxyaldoses
1-Aryl(Glycofurano)imidazolidine-2-Thiones Derived From New 2-(Alkylamino)-2-Deoxyheptoses Having D-Glycero- D-Galacto And D-Glycero-D-Talo Configurations
Acyclic-Sugar Pyrrole C-Nucleoside-Analogs Derived From 2-(Alkylamino)-2-Deoxyaldoses
1-Aryl(Glycofurano)imidazolidine-2-Thiones Derived From New 2-(Alkylamino)-2-Deoxyheptoses Having D-Glycero- D-Galacto And D-Glycero-D-Talo Configurations
Synthesis Of 1-Aryl-(Glycofurano)imidazolidine-2-Thiones From New 2-(Alkylamino)-2-Deoxyhexoses
1-Aryl(Glycofurano)imidazolidine-2-Thiones Derived From New 2-(Alkylamino)-2-Deoxyheptoses Having D-Glycero- D-Galacto And D-Glycero-D-Talo Configurations
Synthesis Of 1-Aryl-(Glycofurano)imidazolidine-2-Thiones From New 2-(Alkylamino)-2-Deoxyhexoses
A Facile Synthesis Of C-Glycosylbarbiturates
Synthesis Of 1-Aryl-(Glycofurano)imidazolidine-2-Thiones From New 2-(Alkylamino)-2-Deoxyhexoses
A Facile Synthesis Of C-Glycosylbarbiturates
Detection Of Inactive Precursors Of Β-Glucanases In Saccharomyces Cerevisiae
A Facile Synthesis Of C-Glycosylbarbiturates
Detection Of Inactive Precursors Of Β-Glucanases In Saccharomyces Cerevisiae
Improving Wine Fermentation Efficiency Of Torulaspora Delbrueckii By Increasing The Ploidy Of Yeast Inocula
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