PUBLICACIÓN

The Castagnoli–Cushman Reaction

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ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Ramiro J.L., Martinez-Caballero S., Neo A.G., Diaz J., Marcos C.F.

2023 MOLECULES

Analytical Chemistry (Q1), Chemistry (miscellaneous) (Q1), Drug Discovery (Q2), Medicine (miscellaneous) (Q2), Molecular Medicine (Q3), Organic Chemistry (Q2), Pharmaceutical Science (Q1), Physical and Theoretical Chemistry (Q2)

JCR: 4.2

SJR: 0.744

CITAS

6

DOI

10.3390/molecules28062654

EID

2-s2.0-85151109854

EISSN

1420-3049

BIBTEX

@article{Ramiro_2023, doi = {10.3390/molecules28062654}, url = {https://doi.org/10.3390%2Fmolecules28062654}, year = 2023, month = {mar}, publisher = {{MDPI} {AG}}, volume = {28}, number = {6}, pages = {2654}, author = {Jos{\'{e}} Luis Ramiro and Sonia Mart{\'{\i}}nez-Caballero and Ana G. Neo and Jes{\'{u}}s D{\'{\i}}az and Carlos F. Marcos}, title = {The Castagnoli{\textendash}Cushman Reaction}, journal = {Molecules}}

AUTORES DE LA UEX

María Sonia Martínez Caballero
Carlos María Fernández Marcos
Jesús Díaz Álvarez
Ana María Gómez Neo

OTRAS PUBLICACIONES DE INTERÉS

Synthesis Of Methyl 4-(2,2-Dimethoxyethyl)-6-Hydroxy-7-Methoxyindole-2-Carboxylate: A Potential Intermediate For The Synthesis Of The Central And Right Parts Of The Anticancer Antibiotic Cc-1065
Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs
A Nuclear Magnetic Resonance Spectroscopy Metabolomic Approach To Renal Dysfunction In Canine Leishmaniasis
Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs
A Nuclear Magnetic Resonance Spectroscopy Metabolomic Approach To Renal Dysfunction In Canine Leishmaniasis
Classification Of Raw Cuts From Iberian And Celta Pigs Based On Lipid Analysis And Chemometrics
A Nuclear Magnetic Resonance Spectroscopy Metabolomic Approach To Renal Dysfunction In Canine Leishmaniasis
Classification Of Raw Cuts From Iberian And Celta Pigs Based On Lipid Analysis And Chemometrics
Elucidation Of The Pyridine Ring-Opening Mechanism Of 2,2′-Bipyridine Or 1,10-Phenanthroline Ligands At Re(I) Carbonyl Complexes
Classification Of Raw Cuts From Iberian And Celta Pigs Based On Lipid Analysis And Chemometrics
Elucidation Of The Pyridine Ring-Opening Mechanism Of 2,2′-Bipyridine Or 1,10-Phenanthroline Ligands At Re(I) Carbonyl Complexes
Machine Learning-Enabled Fatty Acid Quantification And Classification Of Pork From Autochthonous Breeds Using Low-Field 1h Nmr Spectroscopic Data
Elucidation Of The Pyridine Ring-Opening Mechanism Of 2,2′-Bipyridine Or 1,10-Phenanthroline Ligands At Re(I) Carbonyl Complexes
Machine Learning-Enabled Fatty Acid Quantification And Classification Of Pork From Autochthonous Breeds Using Low-Field 1h Nmr Spectroscopic Data
Synthesis Of Coumarin Dimers By A Microwave-Assisted Double Multicomponent Reaction
Machine Learning-Enabled Fatty Acid Quantification And Classification Of Pork From Autochthonous Breeds Using Low-Field 1h Nmr Spectroscopic Data
Synthesis Of Coumarin Dimers By A Microwave-Assisted Double Multicomponent Reaction
Amide-Derived Enols In Enol–ugi Reactions: Expanding Horizons For Peptidomimetic Scaffold Synthesis
Synthesis Of Coumarin Dimers By A Microwave-Assisted Double Multicomponent Reaction
Amide-Derived Enols In Enol–ugi Reactions: Expanding Horizons For Peptidomimetic Scaffold Synthesis
Stefano Marcaccini: A Pioneer In Isocyanide Chemistry
Amide-Derived Enols In Enol–ugi Reactions: Expanding Horizons For Peptidomimetic Scaffold Synthesis
Stefano Marcaccini: A Pioneer In Isocyanide Chemistry
The Castagnoli–cushman Reaction
Stefano Marcaccini: A Pioneer In Isocyanide Chemistry
The Castagnoli–cushman Reaction
Main Group Molecular Switches With Swivel Bifurcated To Trifurcated Hydrogen Bond Mode Of Action
The Castagnoli–cushman Reaction
Main Group Molecular Switches With Swivel Bifurcated To Trifurcated Hydrogen Bond Mode Of Action
Lipidomic Analysis And Classification Of Iberian Dry-Cured Hams With Low Field Nmr
Main Group Molecular Switches With Swivel Bifurcated To Trifurcated Hydrogen Bond Mode Of Action
Lipidomic Analysis And Classification Of Iberian Dry-Cured Hams With Low Field Nmr
1h Nmr To Analyse The Lipid Profile In The Glyceride Fraction Of Different Categories Of Iberian Dry-Cured Hams
Lipidomic Analysis And Classification Of Iberian Dry-Cured Hams With Low Field Nmr
1h Nmr To Analyse The Lipid Profile In The Glyceride Fraction Of Different Categories Of Iberian Dry-Cured Hams
Synthesis Of Imidazolocoumarins By The Amide-Directed Oxidative Cyclisation Of Enol-Ugi Derivatives
1h Nmr To Analyse The Lipid Profile In The Glyceride Fraction Of Different Categories Of Iberian Dry-Cured Hams
Synthesis Of Imidazolocoumarins By The Amide-Directed Oxidative Cyclisation Of Enol-Ugi Derivatives
Pre-Arranged Building Block Approach For The Orthogonal Synthesis Of An Unfolded Tetrameric Organic–inorganic Phosphazane Macrocycle
Synthesis Of Imidazolocoumarins By The Amide-Directed Oxidative Cyclisation Of Enol-Ugi Derivatives
Pre-Arranged Building Block Approach For The Orthogonal Synthesis Of An Unfolded Tetrameric Organic–inorganic Phosphazane Macrocycle
Strongly Electron-Donating Triazolylidene Ligands: Cationic Metal Carbonyl Complexes Of 1-Methyl-1,2,3-Triazole As Triazolium Surrogates
Pre-Arranged Building Block Approach For The Orthogonal Synthesis Of An Unfolded Tetrameric Organic–inorganic Phosphazane Macrocycle
Strongly Electron-Donating Triazolylidene Ligands: Cationic Metal Carbonyl Complexes Of 1-Methyl-1,2,3-Triazole As Triazolium Surrogates
Amide-Stabilized Enols In The Enol-Ugi Reaction: A Five-Component Synthesis Of Triamides
Strongly Electron-Donating Triazolylidene Ligands: Cationic Metal Carbonyl Complexes Of 1-Methyl-1,2,3-Triazole As Triazolium Surrogates
Amide-Stabilized Enols In The Enol-Ugi Reaction: A Five-Component Synthesis Of Triamides
Multicomponent Reactions Of Isocyanides For The Preparation Of Low Molecular Weight Gelators: Preliminary Studies
Amide-Stabilized Enols In The Enol-Ugi Reaction: A Five-Component Synthesis Of Triamides
Multicomponent Reactions Of Isocyanides For The Preparation Of Low Molecular Weight Gelators: Preliminary Studies
Synthesis Of Chromeno[3,4-B]piperazines By An Enol-Ugi/reduction/cyclization Sequence
Multicomponent Reactions Of Isocyanides For The Preparation Of Low Molecular Weight Gelators: Preliminary Studies
Synthesis Of Chromeno[3,4-B]piperazines By An Enol-Ugi/reduction/cyclization Sequence
Size-Control In The Synthesis Of Oxo-Bridged Phosphazane Macrocycles Via A Modular Addition Approach
Synthesis Of Chromeno[3,4-B]piperazines By An Enol-Ugi/reduction/cyclization Sequence
Size-Control In The Synthesis Of Oxo-Bridged Phosphazane Macrocycles Via A Modular Addition Approach
A Safe And Green Benzylic Radical Bromination Experiment
Size-Control In The Synthesis Of Oxo-Bridged Phosphazane Macrocycles Via A Modular Addition Approach
A Safe And Green Benzylic Radical Bromination Experiment
N-Bridged Acyclic Trimeric Poly-Cyclodiphosphazanes: Highly Tuneable Cyclodiphosphazane Building Blocks
A Safe And Green Benzylic Radical Bromination Experiment
N-Bridged Acyclic Trimeric Poly-Cyclodiphosphazanes: Highly Tuneable Cyclodiphosphazane Building Blocks
Influence Of The Nucleophilic Ligand On The Reactivity Of Carbonyl Rhenium(I) Complexes Towards Methyl Propiolate: A Computational Chemistry Perspective
N-Bridged Acyclic Trimeric Poly-Cyclodiphosphazanes: Highly Tuneable Cyclodiphosphazane Building Blocks
Influence Of The Nucleophilic Ligand On The Reactivity Of Carbonyl Rhenium(I) Complexes Towards Methyl Propiolate: A Computational Chemistry Perspective
Addition Of Re-Bonded Nucleophilic Ligands To Activated Alkynes: A Theoretical Rationalization
Influence Of The Nucleophilic Ligand On The Reactivity Of Carbonyl Rhenium(I) Complexes Towards Methyl Propiolate: A Computational Chemistry Perspective
Addition Of Re-Bonded Nucleophilic Ligands To Activated Alkynes: A Theoretical Rationalization
Synthesis Of Heterocyclic Compounds By Photochemical Cyclizations
Addition Of Re-Bonded Nucleophilic Ligands To Activated Alkynes: A Theoretical Rationalization
Synthesis Of Heterocyclic Compounds By Photochemical Cyclizations
Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones
Synthesis Of Heterocyclic Compounds By Photochemical Cyclizations
Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones
Direct Multicomponent Synthesis Of Benzocoumarins
Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones
Direct Multicomponent Synthesis Of Benzocoumarins
Tandem Synthesis Of Polycyclic Isoindoles
Direct Multicomponent Synthesis Of Benzocoumarins
Tandem Synthesis Of Polycyclic Isoindoles
Tandem Synthesis Of 4-Aminoxanthones Is Controlled By A Water-Assisted Tautomerization: A General Straightforward Reaction
Tandem Synthesis Of Polycyclic Isoindoles
Tandem Synthesis Of 4-Aminoxanthones Is Controlled By A Water-Assisted Tautomerization: A General Straightforward Reaction
Regiochemistry Control By Bipyridine Substituents In The Deprotonation Of Rei And Moii N-Alkylimidazole Complexes
Tandem Synthesis Of 4-Aminoxanthones Is Controlled By A Water-Assisted Tautomerization: A General Straightforward Reaction
Regiochemistry Control By Bipyridine Substituents In The Deprotonation Of Rei And Moii N-Alkylimidazole Complexes
Expeditious Multicomponent Synthesis Of Xanthone Dimers
Regiochemistry Control By Bipyridine Substituents In The Deprotonation Of Rei And Moii N-Alkylimidazole Complexes
Expeditious Multicomponent Synthesis Of Xanthone Dimers
Pyrrolidinodiones In Enol-Ugi, Enol-Passerini, And Anomalous Enol-Passerini Condensations
Expeditious Multicomponent Synthesis Of Xanthone Dimers
Pyrrolidinodiones In Enol-Ugi, Enol-Passerini, And Anomalous Enol-Passerini Condensations
Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations
Pyrrolidinodiones In Enol-Ugi, Enol-Passerini, And Anomalous Enol-Passerini Condensations
Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations
Synthesis Of Unique Phosphazane Macrocycles Via Steric Activation Of C-N Bonds
Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations
Synthesis Of Unique Phosphazane Macrocycles Via Steric Activation Of C-N Bonds
Bifunctional Iminophosphorane Catalysed Enantioselective Sulfa-Michael Addition Of Alkyl Thiols To Alkenyl Benzimidazoles
Synthesis Of Unique Phosphazane Macrocycles Via Steric Activation Of C-N Bonds
Bifunctional Iminophosphorane Catalysed Enantioselective Sulfa-Michael Addition Of Alkyl Thiols To Alkenyl Benzimidazoles
An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction
Bifunctional Iminophosphorane Catalysed Enantioselective Sulfa-Michael Addition Of Alkyl Thiols To Alkenyl Benzimidazoles
An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction
Revisiting Trends On Mitochondrial Mega-Channels For The Import Of Proteins And Nucleic Acids
An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction
Revisiting Trends On Mitochondrial Mega-Channels For The Import Of Proteins And Nucleic Acids
Intermolecular C−c Coupling Between 1-Methyl-1,2,3-Triazole And 2,2′-Bipyridine Or 1,10-Phenanthroline In Moii Complexes
Revisiting Trends On Mitochondrial Mega-Channels For The Import Of Proteins And Nucleic Acids
Intermolecular C−c Coupling Between 1-Methyl-1,2,3-Triazole And 2,2′-Bipyridine Or 1,10-Phenanthroline In Moii Complexes
Synthesis And The Optical And Electrochemical Properties Of Indium(Iii) Bis(Arylimino)acenaphthene Complexes
Intermolecular C−c Coupling Between 1-Methyl-1,2,3-Triazole And 2,2′-Bipyridine Or 1,10-Phenanthroline In Moii Complexes
Synthesis And The Optical And Electrochemical Properties Of Indium(Iii) Bis(Arylimino)acenaphthene Complexes
Insights On The Reactivity Of Terminal Phosphanido Metal Complexes Toward Activated Alkynes From Theoretical Computations
Synthesis And The Optical And Electrochemical Properties Of Indium(Iii) Bis(Arylimino)acenaphthene Complexes
Insights On The Reactivity Of Terminal Phosphanido Metal Complexes Toward Activated Alkynes From Theoretical Computations
A Disulfide Bond In The Tim23 Complex Is Crucial For Voltage Gating And Mitochondrial Protein Import
Insights On The Reactivity Of Terminal Phosphanido Metal Complexes Toward Activated Alkynes From Theoretical Computations
A Disulfide Bond In The Tim23 Complex Is Crucial For Voltage Gating And Mitochondrial Protein Import
Regioselective Synthesis Of Dihydroxanthones And Xanthones Through A Tandem Process
A Disulfide Bond In The Tim23 Complex Is Crucial For Voltage Gating And Mitochondrial Protein Import
Regioselective Synthesis Of Dihydroxanthones And Xanthones Through A Tandem Process
Activation Of Aromatic C−c Bonds Of 2,2’-Bipyridine Ligands
Regioselective Synthesis Of Dihydroxanthones And Xanthones Through A Tandem Process
Activation Of Aromatic C−c Bonds Of 2,2’-Bipyridine Ligands
A Multi-Step Solvent-Free Mechanochemical Route To Indium(Iii) Complexes
Activation Of Aromatic C−c Bonds Of 2,2’-Bipyridine Ligands
A Multi-Step Solvent-Free Mechanochemical Route To Indium(Iii) Complexes
Enol-Ugi Reaction Of Hydroxycoumarins: Straightforward Synthesis Of Amino Acid Derived Coumarin Enamines
A Multi-Step Solvent-Free Mechanochemical Route To Indium(Iii) Complexes
Enol-Ugi Reaction Of Hydroxycoumarins: Straightforward Synthesis Of Amino Acid Derived Coumarin Enamines
Regioselective Tandem [4 + 1]-[4 + 2] Synthesis Of Amino-Substituted Dihydroxanthones And Xanthones
Enol-Ugi Reaction Of Hydroxycoumarins: Straightforward Synthesis Of Amino Acid Derived Coumarin Enamines
Regioselective Tandem [4 + 1]-[4 + 2] Synthesis Of Amino-Substituted Dihydroxanthones And Xanthones
Influence Of The N-N Coligand: C-C Coupling Instead Of Formation Of Imidazol-2-Yl Complexes At {Mo(Η3-Allyl)(Co)2} Fragments. Theoretical And Experimental Studies
Regioselective Tandem [4 + 1]-[4 + 2] Synthesis Of Amino-Substituted Dihydroxanthones And Xanthones
Influence Of The N-N Coligand: C-C Coupling Instead Of Formation Of Imidazol-2-Yl Complexes At {Mo(Η3-Allyl)(Co)2} Fragments. Theoretical And Experimental Studies
Steric C-N Bond Activation On The Dimeric Macrocycle [{P(Μ-Nr)}2(Μ-Nr)]2
Influence Of The N-N Coligand: C-C Coupling Instead Of Formation Of Imidazol-2-Yl Complexes At {Mo(Η3-Allyl)(Co)2} Fragments. Theoretical And Experimental Studies
Steric C-N Bond Activation On The Dimeric Macrocycle [{P(Μ-Nr)}2(Μ-Nr)]2
Synthesis Of 4-Aminoxanthones By An Uncatalyzed, Multicomponent Reaction
Steric C-N Bond Activation On The Dimeric Macrocycle [{P(Μ-Nr)}2(Μ-Nr)]2
Synthesis Of 4-Aminoxanthones By An Uncatalyzed, Multicomponent Reaction
Allylic Amination Of Passerini Adducts. Application To The Selective Synthesis Of Chromone-Substituted Α-And Γ-Amino Acid Peptidic And Retropeptidic Units
Synthesis Of 4-Aminoxanthones By An Uncatalyzed, Multicomponent Reaction
Allylic Amination Of Passerini Adducts. Application To The Selective Synthesis Of Chromone-Substituted Α-And Γ-Amino Acid Peptidic And Retropeptidic Units
Elusive 2-Aminofuran Diels-Alder Substrates For A Straightforward Synthesis Of Polysubstituted Anilines
Allylic Amination Of Passerini Adducts. Application To The Selective Synthesis Of Chromone-Substituted Α-And Γ-Amino Acid Peptidic And Retropeptidic Units
Elusive 2-Aminofuran Diels-Alder Substrates For A Straightforward Synthesis Of Polysubstituted Anilines
Copper-Catalyzed Addition Of Nucleophilic Silicon To Aldehydes
Elusive 2-Aminofuran Diels-Alder Substrates For A Straightforward Synthesis Of Polysubstituted Anilines
Copper-Catalyzed Addition Of Nucleophilic Silicon To Aldehydes
Studies On The Synthesis Of A Hindered Analogue Of The Antitumour Agent Cc-1065
Copper-Catalyzed Addition Of Nucleophilic Silicon To Aldehydes
Studies On The Synthesis Of A Hindered Analogue Of The Antitumour Agent Cc-1065
Bax And Bak Function As The Outer Membrane Component Of The Mitochondrial Permeability Pore In Regulating Necrotic Cell Death In Mice
Studies On The Synthesis Of A Hindered Analogue Of The Antitumour Agent Cc-1065
Bax And Bak Function As The Outer Membrane Component Of The Mitochondrial Permeability Pore In Regulating Necrotic Cell Death In Mice
Enols As Feasible Acid Components In The Ugi Condensation
Bax And Bak Function As The Outer Membrane Component Of The Mitochondrial Permeability Pore In Regulating Necrotic Cell Death In Mice
Enols As Feasible Acid Components In The Ugi Condensation
Furo[3,4-B]chromones, And Not Pyrano[3,4-B]chromones, Are Obtained By The Reaction Of 3-Formylchromones With Isocyanides
Enols As Feasible Acid Components In The Ugi Condensation
Furo[3,4-B]chromones, And Not Pyrano[3,4-B]chromones, Are Obtained By The Reaction Of 3-Formylchromones With Isocyanides
Conjugate Addition Of Isocyanides To Chromone 3-Carboxylic Acid: An Efficient One-Pot Synthesis Of Chroman-4-One 2-Carboxamides
Furo[3,4-B]chromones, And Not Pyrano[3,4-B]chromones, Are Obtained By The Reaction Of 3-Formylchromones With Isocyanides
Conjugate Addition Of Isocyanides To Chromone 3-Carboxylic Acid: An Efficient One-Pot Synthesis Of Chroman-4-One 2-Carboxamides
A Straightforward Synthesis Of 2-Aminobenzothiazoles From Herz Compounds
Conjugate Addition Of Isocyanides To Chromone 3-Carboxylic Acid: An Efficient One-Pot Synthesis Of Chroman-4-One 2-Carboxamides
A Straightforward Synthesis Of 2-Aminobenzothiazoles From Herz Compounds
A Multicomponent Approach To The Synthesis Of 1,3-Dicarbonylic Compounds
A Straightforward Synthesis Of 2-Aminobenzothiazoles From Herz Compounds
A Multicomponent Approach To The Synthesis Of 1,3-Dicarbonylic Compounds
Two Different Hydrogen Bond Donor Ligands Together: A Selectivity Improvement In Organometallic {Re(Co) 3} Anion Hosts
A Multicomponent Approach To The Synthesis Of 1,3-Dicarbonylic Compounds
Two Different Hydrogen Bond Donor Ligands Together: A Selectivity Improvement In Organometallic {Re(Co) 3} Anion Hosts
Imidazole To Nhc Rearrangements At Molybdenum Centers: An Experimental And Theoretical Study
Two Different Hydrogen Bond Donor Ligands Together: A Selectivity Improvement In Organometallic {Re(Co) 3} Anion Hosts
Imidazole To Nhc Rearrangements At Molybdenum Centers: An Experimental And Theoretical Study
Proline-Catalyzed Aldol Reactions Of Cyclic Diketones: Fluorine Modifies Pathways As Well As Transition States
Imidazole To Nhc Rearrangements At Molybdenum Centers: An Experimental And Theoretical Study
Proline-Catalyzed Aldol Reactions Of Cyclic Diketones: Fluorine Modifies Pathways As Well As Transition States
From Bis(N-Alkylimidazole) To Bis(Nh-Nhc) In Rhenium Carbonyl Complexes
Proline-Catalyzed Aldol Reactions Of Cyclic Diketones: Fluorine Modifies Pathways As Well As Transition States
From Bis(N-Alkylimidazole) To Bis(Nh-Nhc) In Rhenium Carbonyl Complexes
Effect Of The Nature Of The Substituent In N-Alkylimidazole Ligands On The Outcome Of Deprotonation: Ring Opening Versus The Formation Of N-Heterocyclic Carbene Complexes
From Bis(N-Alkylimidazole) To Bis(Nh-Nhc) In Rhenium Carbonyl Complexes
Effect Of The Nature Of The Substituent In N-Alkylimidazole Ligands On The Outcome Of Deprotonation: Ring Opening Versus The Formation Of N-Heterocyclic Carbene Complexes
Preparation Of Phenanthrenes By Photocyclization Of Stilbenes Containing A Tosyl Group On The Central Double Bond. A Versatile Approach To The Synthesis Of Phenanthrenes And Phenanthrenoids
Effect Of The Nature Of The Substituent In N-Alkylimidazole Ligands On The Outcome Of Deprotonation: Ring Opening Versus The Formation Of N-Heterocyclic Carbene Complexes
Preparation Of Phenanthrenes By Photocyclization Of Stilbenes Containing A Tosyl Group On The Central Double Bond. A Versatile Approach To The Synthesis Of Phenanthrenes And Phenanthrenoids
Simple 1-Dicyanomethylene-2-Chloro-3-Aminoindene Push-Pull Chromophores: Applications In Cation And Anion Sensing
Preparation Of Phenanthrenes By Photocyclization Of Stilbenes Containing A Tosyl Group On The Central Double Bond. A Versatile Approach To The Synthesis Of Phenanthrenes And Phenanthrenoids
Simple 1-Dicyanomethylene-2-Chloro-3-Aminoindene Push-Pull Chromophores: Applications In Cation And Anion Sensing
Mac And Bcl-2 Family Proteins Conspire In A Deadly Plot
Simple 1-Dicyanomethylene-2-Chloro-3-Aminoindene Push-Pull Chromophores: Applications In Cation And Anion Sensing
Mac And Bcl-2 Family Proteins Conspire In A Deadly Plot
Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones
Mac And Bcl-2 Family Proteins Conspire In A Deadly Plot
Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones
Photocyclization Of Tosylstilbenes As A Key Reaction In The Preparation Of An Analogue Of The Antitumor Agent Cc-1065
Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones
Photocyclization Of Tosylstilbenes As A Key Reaction In The Preparation Of An Analogue Of The Antitumor Agent Cc-1065
Nanoscale Aggregation Phenomena At The Contact Line Of Air-Drying Pure Water Droplets On Silicon Revealed By Atomic Force Microscopy
Photocyclization Of Tosylstilbenes As A Key Reaction In The Preparation Of An Analogue Of The Antitumor Agent Cc-1065
Nanoscale Aggregation Phenomena At The Contact Line Of Air-Drying Pure Water Droplets On Silicon Revealed By Atomic Force Microscopy
Assembly Of The Mitochondrial Apoptosis-Induced Channel, Mac
Nanoscale Aggregation Phenomena At The Contact Line Of Air-Drying Pure Water Droplets On Silicon Revealed By Atomic Force Microscopy
Assembly Of The Mitochondrial Apoptosis-Induced Channel, Mac
Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation
Assembly Of The Mitochondrial Apoptosis-Induced Channel, Mac
Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation
Ugi Four-Component Condensation With Two Cleavable Components: The Easiest Synthesis Of 2,n-Diarylglycines
Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation
Ugi Four-Component Condensation With Two Cleavable Components: The Easiest Synthesis Of 2,n-Diarylglycines
Multicomponent Synthesis Of Highly Substituted 2-Pyridones
Ugi Four-Component Condensation With Two Cleavable Components: The Easiest Synthesis Of 2,n-Diarylglycines
Multicomponent Synthesis Of Highly Substituted 2-Pyridones
Erratum: The Nuclear Receptor Interacting Factor-3 Transcriptional Coregulator Mediates Rapid Apoptosis In Breast Cancer Cells Through Direct And Bystander-Mediated Events (Cancer Research (2007) 67, (1775-1782))
Multicomponent Synthesis Of Highly Substituted 2-Pyridones
Erratum: The Nuclear Receptor Interacting Factor-3 Transcriptional Coregulator Mediates Rapid Apoptosis In Breast Cancer Cells Through Direct And Bystander-Mediated Events (Cancer Research (2007) 67, (1775-1782))
A Fluorescence Assay For Peptide Translocation Into Mitochondria
Erratum: The Nuclear Receptor Interacting Factor-3 Transcriptional Coregulator Mediates Rapid Apoptosis In Breast Cancer Cells Through Direct And Bystander-Mediated Events (Cancer Research (2007) 67, (1775-1782))
A Fluorescence Assay For Peptide Translocation Into Mitochondria
The Nuclear Receptor Interacting Factor-3 Transcriptional Coregulator Mediates Rapid Apoptosis In Breast Cancer Cells Through Direct And Bystander-Mediated Events
A Fluorescence Assay For Peptide Translocation Into Mitochondria
The Nuclear Receptor Interacting Factor-3 Transcriptional Coregulator Mediates Rapid Apoptosis In Breast Cancer Cells Through Direct And Bystander-Mediated Events
Tim17p Regulates The Twin Pore Structure And Voltage Gating Of The Mitochondrial Protein Import Complex Tim23
The Nuclear Receptor Interacting Factor-3 Transcriptional Coregulator Mediates Rapid Apoptosis In Breast Cancer Cells Through Direct And Bystander-Mediated Events
Tim17p Regulates The Twin Pore Structure And Voltage Gating Of The Mitochondrial Protein Import Complex Tim23
Photodynamic Cell-Kill Analysis Of Breast Tumor Cells With A Tamoxifen-Pyropheophorbide Conjugate
Tim17p Regulates The Twin Pore Structure And Voltage Gating Of The Mitochondrial Protein Import Complex Tim23
Photodynamic Cell-Kill Analysis Of Breast Tumor Cells With A Tamoxifen-Pyropheophorbide Conjugate
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Photodynamic Cell-Kill Analysis Of Breast Tumor Cells With A Tamoxifen-Pyropheophorbide Conjugate
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Ultrastructural And Physico-Chemical Heterogeneities Of Yeast Surfaces Revealed By Mapping Lateral-Friction And Normal-Adhesion Forces Using An Atomic Force Microscope
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Ultrastructural And Physico-Chemical Heterogeneities Of Yeast Surfaces Revealed By Mapping Lateral-Friction And Normal-Adhesion Forces Using An Atomic Force Microscope
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Ultrastructural And Physico-Chemical Heterogeneities Of Yeast Surfaces Revealed By Mapping Lateral-Friction And Normal-Adhesion Forces Using An Atomic Force Microscope
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Tert-Butyl Isocyanide
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Tert-Butyl Isocyanide
Is Mac The Knife That Cuts Cytochrome C From Mitochondria During Apoptosis?
Tert-Butyl Isocyanide
Is Mac The Knife That Cuts Cytochrome C From Mitochondria During Apoptosis?
Regulation Of The Mitochondrial Apoptosis-Induced Channel, Mac, By Bcl-2 Family Proteins
Is Mac The Knife That Cuts Cytochrome C From Mitochondria During Apoptosis?
Regulation Of The Mitochondrial Apoptosis-Induced Channel, Mac, By Bcl-2 Family Proteins
Detection Of The Mitochondrial Apoptosis-Induced Channel (Mac) And Its Regulation By Bcl-2 Family Proteins.
Regulation Of The Mitochondrial Apoptosis-Induced Channel, Mac, By Bcl-2 Family Proteins
Detection Of The Mitochondrial Apoptosis-Induced Channel (Mac) And Its Regulation By Bcl-2 Family Proteins.
Studies On Isocyanides. A Facile Synthesis Of 4,5-Dihydro-1,4- Benzothiazepin-3(2h)-Ones Via Post-Condensation Modifications Of The Ugi Reaction
Detection Of The Mitochondrial Apoptosis-Induced Channel (Mac) And Its Regulation By Bcl-2 Family Proteins.
Studies On Isocyanides. A Facile Synthesis Of 4,5-Dihydro-1,4- Benzothiazepin-3(2h)-Ones Via Post-Condensation Modifications Of The Ugi Reaction
Indene And Pseudoazulene Discotic Liquid Crystals: A Synthetic And Structural Study
Studies On Isocyanides. A Facile Synthesis Of 4,5-Dihydro-1,4- Benzothiazepin-3(2h)-Ones Via Post-Condensation Modifications Of The Ugi Reaction
Indene And Pseudoazulene Discotic Liquid Crystals: A Synthetic And Structural Study
A New Synthesis Of Β-Keto Amides By Reduction Of Passerini Adducts
Indene And Pseudoazulene Discotic Liquid Crystals: A Synthetic And Structural Study
A New Synthesis Of Β-Keto Amides By Reduction Of Passerini Adducts
Computer-Assisted Design Of Asymmetric 1,3-Dipolar Cycloadditions Between Dimethylvinylborane And Chiral Nitrones
A New Synthesis Of Β-Keto Amides By Reduction Of Passerini Adducts
Computer-Assisted Design Of Asymmetric 1,3-Dipolar Cycloadditions Between Dimethylvinylborane And Chiral Nitrones
The Role Of The Mitochondrial Apoptosis Induced Channel Mac In Cytochrome C Release
Computer-Assisted Design Of Asymmetric 1,3-Dipolar Cycloadditions Between Dimethylvinylborane And Chiral Nitrones
The Role Of The Mitochondrial Apoptosis Induced Channel Mac In Cytochrome C Release
Oligomeric Bax Is A Component Of The Putative Cytochrome C Release Channel Mac, Mitochondrial Apoptosis-Induced Channel
The Role Of The Mitochondrial Apoptosis Induced Channel Mac In Cytochrome C Release
Oligomeric Bax Is A Component Of The Putative Cytochrome C Release Channel Mac, Mitochondrial Apoptosis-Induced Channel
Cyclopentathiadiazines, Cyclohepta- And Cyclopentadithiazoles: New Materials And A Rich Heterocyclic Chemistry Of Cyclic Enaminonitriles
Oligomeric Bax Is A Component Of The Putative Cytochrome C Release Channel Mac, Mitochondrial Apoptosis-Induced Channel
Cyclopentathiadiazines, Cyclohepta- And Cyclopentadithiazoles: New Materials And A Rich Heterocyclic Chemistry Of Cyclic Enaminonitriles
Cyclopentathiadiazines, New Heterocyclic Materials From Cyclic Enaminonitriles
Cyclopentathiadiazines, Cyclohepta- And Cyclopentadithiazoles: New Materials And A Rich Heterocyclic Chemistry Of Cyclic Enaminonitriles
Cyclopentathiadiazines, New Heterocyclic Materials From Cyclic Enaminonitriles
Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles
Cyclopentathiadiazines, New Heterocyclic Materials From Cyclic Enaminonitriles
Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Some Amphiphilic Cations Block The Mitochondrial Apoptosis-Induced Channel, Mac
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Some Amphiphilic Cations Block The Mitochondrial Apoptosis-Induced Channel, Mac
Electrophysiological Approaches To The Study Of Protein Translocation In Mitochondria
Some Amphiphilic Cations Block The Mitochondrial Apoptosis-Induced Channel, Mac
Electrophysiological Approaches To The Study Of Protein Translocation In Mitochondria
Affinity Labeling Of The Nuclear Vitamin D Receptor With Nonsteroidal Alkylating Agents
Electrophysiological Approaches To The Study Of Protein Translocation In Mitochondria
Affinity Labeling Of The Nuclear Vitamin D Receptor With Nonsteroidal Alkylating Agents
Infrared Spectroscopy In The Study Of Renal Lithiasis
Affinity Labeling Of The Nuclear Vitamin D Receptor With Nonsteroidal Alkylating Agents
Infrared Spectroscopy In The Study Of Renal Lithiasis
Studies On Isocyanides And Related Compounds; A Facile Synthesis Of Functionalized 3(2h)-Pyridazinones Via Ugi Four-Component Condensation
Infrared Spectroscopy In The Study Of Renal Lithiasis
Studies On Isocyanides And Related Compounds; A Facile Synthesis Of Functionalized 3(2h)-Pyridazinones Via Ugi Four-Component Condensation
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Studies On Isocyanides And Related Compounds; A Facile Synthesis Of Functionalized 3(2h)-Pyridazinones Via Ugi Four-Component Condensation
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Base-Induced Photocyclization Of 1,2-Diaryl-1-Tosylethenes. A Mechanistically Novel Approach To Phenanthrenes And Phenanthrenoids
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Base-Induced Photocyclization Of 1,2-Diaryl-1-Tosylethenes. A Mechanistically Novel Approach To Phenanthrenes And Phenanthrenoids
A New Addition-Rearrangement Of [1,4]thiazine-2-Thiones With Aryl-1,2,4-Triazoline-3,5-Diones
Base-Induced Photocyclization Of 1,2-Diaryl-1-Tosylethenes. A Mechanistically Novel Approach To Phenanthrenes And Phenanthrenoids
A New Addition-Rearrangement Of [1,4]thiazine-2-Thiones With Aryl-1,2,4-Triazoline-3,5-Diones
Synthesis Of Poly-Ferrocene Heterocycles By Cycloaddition Of Mono- Or Bis(Ferrocenecarbonyl)acetylenes And Bis[1,2]dithiolo[1,4]thiazinethiones
A New Addition-Rearrangement Of [1,4]thiazine-2-Thiones With Aryl-1,2,4-Triazoline-3,5-Diones
Synthesis Of Poly-Ferrocene Heterocycles By Cycloaddition Of Mono- Or Bis(Ferrocenecarbonyl)acetylenes And Bis[1,2]dithiolo[1,4]thiazinethiones
Synthesis Of [1,3]dithiole And Spiro[1,3] Dithiole Thiopyran Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
Synthesis Of Poly-Ferrocene Heterocycles By Cycloaddition Of Mono- Or Bis(Ferrocenecarbonyl)acetylenes And Bis[1,2]dithiolo[1,4]thiazinethiones
Synthesis Of [1,3]dithiole And Spiro[1,3] Dithiole Thiopyran Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
Lesions Induced By 2,4-D And Chlorpyrifos In Tench (Tinca Tinca L.): Implication In Toxicity Studies
Synthesis Of [1,3]dithiole And Spiro[1,3] Dithiole Thiopyran Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
Lesions Induced By 2,4-D And Chlorpyrifos In Tench (Tinca Tinca L.): Implication In Toxicity Studies
New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles
Lesions Induced By 2,4-D And Chlorpyrifos In Tench (Tinca Tinca L.): Implication In Toxicity Studies
New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles
Derivatives Of Methyl 5-Methyl-4-Oxo-1,2,4,5,8,8a-Hexahydrocyclopropa[C]-Pyrrolo[3,2-E] Indole-7-Carboxylate: A Case Of Inverse Electronic Effects On The Reactivity Of Cc-1065 Derivatives
New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles
Derivatives Of Methyl 5-Methyl-4-Oxo-1,2,4,5,8,8a-Hexahydrocyclopropa[C]-Pyrrolo[3,2-E] Indole-7-Carboxylate: A Case Of Inverse Electronic Effects On The Reactivity Of Cc-1065 Derivatives
Synthesis Of Thiadiazole, Dithietane, And Imine Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
Derivatives Of Methyl 5-Methyl-4-Oxo-1,2,4,5,8,8a-Hexahydrocyclopropa[C]-Pyrrolo[3,2-E] Indole-7-Carboxylate: A Case Of Inverse Electronic Effects On The Reactivity Of Cc-1065 Derivatives
Synthesis Of Thiadiazole, Dithietane, And Imine Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
Ultrastructural Study Of Ovine Pulmonary Pasteurellosis: Involvement Of Neutrophils And Macrophages
Synthesis Of Thiadiazole, Dithietane, And Imine Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
Ultrastructural Study Of Ovine Pulmonary Pasteurellosis: Involvement Of Neutrophils And Macrophages
Glu-256 Is A Main Structural Determinant For Oligomerisation Of Human Arginase I
Ultrastructural Study Of Ovine Pulmonary Pasteurellosis: Involvement Of Neutrophils And Macrophages
Glu-256 Is A Main Structural Determinant For Oligomerisation Of Human Arginase I
Multicomponent Reactions: A Convenient Undergraduate Organic Chemistry Experiment
Glu-256 Is A Main Structural Determinant For Oligomerisation Of Human Arginase I
Multicomponent Reactions: A Convenient Undergraduate Organic Chemistry Experiment
Studies On Isocyanides And Related Compounds. Synthesis Of Furan Derivatives And Their Transformation Into Indole Derivatives
Multicomponent Reactions: A Convenient Undergraduate Organic Chemistry Experiment
Studies On Isocyanides And Related Compounds. Synthesis Of Furan Derivatives And Their Transformation Into Indole Derivatives
2,4-D Treatment In Tench (Tinca Tinca L.): Pathological Processes On The Excretory Kidney
Studies On Isocyanides And Related Compounds. Synthesis Of Furan Derivatives And Their Transformation Into Indole Derivatives
2,4-D Treatment In Tench (Tinca Tinca L.): Pathological Processes On The Excretory Kidney
Synthesis Of Bis[1,2]dithiolo[1,4]thiazines And A [1,2]dithiolo[1,4]thiazine From Tertiary Diisopropylamines
2,4-D Treatment In Tench (Tinca Tinca L.): Pathological Processes On The Excretory Kidney
Synthesis Of Bis[1,2]dithiolo[1,4]thiazines And A [1,2]dithiolo[1,4]thiazine From Tertiary Diisopropylamines
Synthesis Of Sulfur-Rich 1,2-And 1,3-Dithiolo Disulfides And Thiodesaurines From Diisopropyl Sulfide
Synthesis Of Bis[1,2]dithiolo[1,4]thiazines And A [1,2]dithiolo[1,4]thiazine From Tertiary Diisopropylamines
Synthesis Of Sulfur-Rich 1,2-And 1,3-Dithiolo Disulfides And Thiodesaurines From Diisopropyl Sulfide
Bis[1,2]dithiolo[3,4-B][4',3'-E][1,4]thiazine-3,5-Dione, A Planar 1,4-Thiazine
Synthesis Of Sulfur-Rich 1,2-And 1,3-Dithiolo Disulfides And Thiodesaurines From Diisopropyl Sulfide
Bis[1,2]dithiolo[3,4-B][4',3'-E][1,4]thiazine-3,5-Dione, A Planar 1,4-Thiazine
Conversion Of W-Alkyldiisopropylàmines Into Yv,/v-Bis(5-Chloro-3-Oxo[1,2]dithiol-4-Yl)amines
Bis[1,2]dithiolo[3,4-B][4',3'-E][1,4]thiazine-3,5-Dione, A Planar 1,4-Thiazine
Conversion Of W-Alkyldiisopropylàmines Into Yv,/v-Bis(5-Chloro-3-Oxo[1,2]dithiol-4-Yl)amines
Acute 2,4-D Poisoning In Tench (Tinca Tinca L.): Lesions In The Hematopoietic Portion Of The Kidney
Conversion Of W-Alkyldiisopropylàmines Into Yv,/v-Bis(5-Chloro-3-Oxo[1,2]dithiol-4-Yl)amines
Acute 2,4-D Poisoning In Tench (Tinca Tinca L.): Lesions In The Hematopoietic Portion Of The Kidney
Asymmetric Synthesis And Electrochemical Behaviour Of A C2 Chiral Bisferrocenyl Orthoquinone
Acute 2,4-D Poisoning In Tench (Tinca Tinca L.): Lesions In The Hematopoietic Portion Of The Kidney
Asymmetric Synthesis And Electrochemical Behaviour Of A C2 Chiral Bisferrocenyl Orthoquinone
Histopathological Lesions In Tench, Tinca Tinca (L.) Kidney Followiong Exposure To Chlorpyrifos
Asymmetric Synthesis And Electrochemical Behaviour Of A C2 Chiral Bisferrocenyl Orthoquinone
Histopathological Lesions In Tench, Tinca Tinca (L.) Kidney Followiong Exposure To Chlorpyrifos
Selective Syntheses Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles From Hünig's Base
Histopathological Lesions In Tench, Tinca Tinca (L.) Kidney Followiong Exposure To Chlorpyrifos
Selective Syntheses Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles From Hünig's Base
Tertiary Amine-S2cl2 Chemistry: Interception Of Reaction Intermediates
Selective Syntheses Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles From Hünig's Base
Tertiary Amine-S2cl2 Chemistry: Interception Of Reaction Intermediates
A Facile Synthesis Of Β-Lactams Based On The Isocyanide Chemistry
Tertiary Amine-S2cl2 Chemistry: Interception Of Reaction Intermediates
A Facile Synthesis Of Β-Lactams Based On The Isocyanide Chemistry
From Hünig's Base To Bis([1,2]dithiolo)- [1,4]thiazines In One Pot: The Fast Route To Highly Sulfurated Heterocycles
A Facile Synthesis Of Β-Lactams Based On The Isocyanide Chemistry
From Hünig's Base To Bis([1,2]dithiolo)- [1,4]thiazines In One Pot: The Fast Route To Highly Sulfurated Heterocycles
Studies On Isocyanides And Related Compounds. An Unusual Synthesis Of Functionalized Succinimides
From Hünig's Base To Bis([1,2]dithiolo)- [1,4]thiazines In One Pot: The Fast Route To Highly Sulfurated Heterocycles
Studies On Isocyanides And Related Compounds. An Unusual Synthesis Of Functionalized Succinimides
One-Pot Synthesis And Chemistry Of Bis[1,2]dithiolopyrroles
Studies On Isocyanides And Related Compounds. An Unusual Synthesis Of Functionalized Succinimides
One-Pot Synthesis And Chemistry Of Bis[1,2]dithiolopyrroles
Studies On Isocyanides And Related Compounds. A Novel Synthetic Route To 1,6-Dihydro-6-Oxopyridine-2-Carboxylic Acid Derivatives
One-Pot Synthesis And Chemistry Of Bis[1,2]dithiolopyrroles
Studies On Isocyanides And Related Compounds. A Novel Synthetic Route To 1,6-Dihydro-6-Oxopyridine-2-Carboxylic Acid Derivatives
Studies On The Synthesis Of The Antitumor Agent Cc-1065: Preparation Of Isopropyl 6-Hydroxy-7-Methoxy-4-(2-Nitrooxyethyl)indole-2-Carboxylate
Studies On Isocyanides And Related Compounds. A Novel Synthetic Route To 1,6-Dihydro-6-Oxopyridine-2-Carboxylic Acid Derivatives
Studies On The Synthesis Of The Antitumor Agent Cc-1065: Preparation Of Isopropyl 6-Hydroxy-7-Methoxy-4-(2-Nitrooxyethyl)indole-2-Carboxylate
Synthesis Of Enantiomerically Pure Tricarbonylchromium(0) Complexes Of Ortho Substituted Styrenes From S‐α‐methylbenzylamine
Studies On The Synthesis Of The Antitumor Agent Cc-1065: Preparation Of Isopropyl 6-Hydroxy-7-Methoxy-4-(2-Nitrooxyethyl)indole-2-Carboxylate
Synthesis Of Enantiomerically Pure Tricarbonylchromium(0) Complexes Of Ortho Substituted Styrenes From S‐α‐methylbenzylamine
Phenol Nitration From A 2-(Nitrooxy)ethyl Side Chain
Synthesis Of Enantiomerically Pure Tricarbonylchromium(0) Complexes Of Ortho Substituted Styrenes From S‐α‐methylbenzylamine
Phenol Nitration From A 2-(Nitrooxy)ethyl Side Chain
Organometallics In Synthesis. Part I: The Transition Elements
Phenol Nitration From A 2-(Nitrooxy)ethyl Side Chain
Organometallics In Synthesis. Part I: The Transition Elements
Spontaneous Bovine Respiratory Syncytial Virus Infection In Goats: Pathological Findings
Organometallics In Synthesis. Part I: The Transition Elements
Spontaneous Bovine Respiratory Syncytial Virus Infection In Goats: Pathological Findings
First Synthesis Of Sulfonyl Substituted Tricarbonyl(Η6- Arene)chromium(0) Complexed
Spontaneous Bovine Respiratory Syncytial Virus Infection In Goats: Pathological Findings
First Synthesis Of Sulfonyl Substituted Tricarbonyl(Η6- Arene)chromium(0) Complexed
Sulfoxides And Stereochemical Control In Organometallic Chemistry
First Synthesis Of Sulfonyl Substituted Tricarbonyl(Η6- Arene)chromium(0) Complexed
Sulfoxides And Stereochemical Control In Organometallic Chemistry
The Immunologic Response To Experimental Infection With Bovine Respiratory Syncytial Virus In Lambs
Sulfoxides And Stereochemical Control In Organometallic Chemistry
The Immunologic Response To Experimental Infection With Bovine Respiratory Syncytial Virus In Lambs
Synthesis Of Tricarbonyliron(0) Complexes Of Itaconic Acid Derivatives
The Immunologic Response To Experimental Infection With Bovine Respiratory Syncytial Virus In Lambs
Synthesis Of Tricarbonyliron(0) Complexes Of Itaconic Acid Derivatives
New One-Pot Synthesis Of Alkyl Nitrates From Alcohols
Synthesis Of Tricarbonyliron(0) Complexes Of Itaconic Acid Derivatives
New One-Pot Synthesis Of Alkyl Nitrates From Alcohols
Synthesis Of Methyl 4-(2,2-Dimethoxyethyl)-6-Hydroxy-7-Methoxyindole-2-Carboxylate: A Potential Intermediate For The Synthesis Of The Central And Right Parts Of The Anticancer Antibiotic Cc-1065
New One-Pot Synthesis Of Alkyl Nitrates From Alcohols
Synthesis Of Methyl 4-(2,2-Dimethoxyethyl)-6-Hydroxy-7-Methoxyindole-2-Carboxylate: A Potential Intermediate For The Synthesis Of The Central And Right Parts Of The Anticancer Antibiotic Cc-1065
Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs
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