Portal Investigación UEx

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

Machine Learning-Enabled Fatty Acid Quantification And Classification Of Pork From Autochthonous Breeds Using Low-Field 1h Nmr Spectroscopic Data

Classification Of Raw Cuts From Iberian And Celta Pigs Based On Lipid Analysis And Chemometrics

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

Lipidomic Analysis And Classification Of Iberian Dry-Cured Hams With Low Field Nmr

The Castagnoli–cushman Reaction

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

Amide-Stabilized Enols In The Enol-Ugi Reaction: A Five-Component Synthesis Of Triamides

Synthesis Of Imidazolocoumarins By The Amide-Directed Oxidative Cyclisation Of Enol-Ugi Derivatives

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

A Safe And Green Benzylic Radical Bromination Experiment

Synthesis Of Chromeno[3,4-B]piperazines By An Enol-Ugi/reduction/cyclization Sequence

A Safe And Green Benzylic Radical Bromination Experiment

Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones

A Safe And Green Benzylic Radical Bromination Experiment

Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones

Tandem Synthesis Of Polycyclic Isoindoles

Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones

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

Expeditious Multicomponent Synthesis Of Xanthone Dimers

Tandem Synthesis Of 4-Aminoxanthones Is Controlled By A Water-Assisted Tautomerization: A General Straightforward Reaction

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

An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction

Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations

An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction

Enol-Ugi Reaction Of Hydroxycoumarins: Straightforward Synthesis Of Amino Acid Derived Coumarin Enamines

An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction

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

Synthesis Of 4-Aminoxanthones By An Uncatalyzed, Multicomponent Reaction

Regioselective Tandem [4 + 1]-[4 + 2] Synthesis Of Amino-Substituted Dihydroxanthones And Xanthones

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

Enols As Feasible Acid Components In The Ugi Condensation

Elusive 2-Aminofuran Diels-Alder Substrates For A Straightforward Synthesis Of Polysubstituted Anilines

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

Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones

A Multicomponent Approach To The Synthesis Of 1,3-Dicarbonylic Compounds

Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones

Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation

Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones

Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation

Multicomponent Synthesis Of Highly Substituted 2-Pyridones

Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation

Multicomponent Synthesis Of Highly Substituted 2-Pyridones

Photodynamic Cell-Kill Analysis Of Breast Tumor Cells With A Tamoxifen-Pyropheophorbide Conjugate

Multicomponent Synthesis Of Highly Substituted 2-Pyridones

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

Tert-Butyl Isocyanide

Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives

Tert-Butyl Isocyanide

Studies On Isocyanides. A Facile Synthesis Of 4,5-Dihydro-1,4- Benzothiazepin-3(2h)-Ones Via Post-Condensation Modifications Of The Ugi Reaction

Tert-Butyl Isocyanide

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

Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles

A New Synthesis Of Β-Keto Amides By Reduction Of Passerini Adducts

Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles

Affinity Labeling Of The Nuclear Vitamin D Receptor With Nonsteroidal Alkylating Agents

Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles

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

Synthesis Of Poly-Ferrocene Heterocycles By Cycloaddition Of Mono- Or Bis(Ferrocenecarbonyl)acetylenes And Bis[1,2]dithiolo[1,4]thiazinethiones

Studies On Isocyanides And Related Compounds; A Facile Synthesis Of Functionalized 3(2h)-Pyridazinones Via Ugi Four-Component Condensation

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

New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles

Synthesis Of [1,3]dithiole And Spiro[1,3] Dithiole Thiopyran Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System

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

Glu-256 Is A Main Structural Determinant For Oligomerisation Of Human Arginase I

Synthesis Of Thiadiazole, Dithietane, And Imine Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System

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

Synthesis Of Bis[1,2]dithiolo[1,4]thiazines And A [1,2]dithiolo[1,4]thiazine From Tertiary Diisopropylamines

Studies On Isocyanides And Related Compounds. Synthesis Of Furan Derivatives And Their Transformation Into Indole Derivatives

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

Selective Syntheses Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles From Hünig's Base

Conversion Of W-Alkyldiisopropylàmines Into Yv,/v-Bis(5-Chloro-3-Oxo[1,2]dithiol-4-Yl)amines

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

First Synthesis Of Sulfonyl Substituted Tricarbonyl(Η6- Arene)chromium(0) Complexed

Organometallics In Synthesis. Part I: The Transition Elements

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

Synthesis Of Tricarbonyliron(0) Complexes Of Itaconic Acid Derivatives

Sulfoxides And Stereochemical Control In Organometallic Chemistry

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