Amanote Research
Register
Sign In
Azabicyclic Amino Acids by Stereoselective Dearomatizing Cyclization of the Enolates of N-Nicotinoyl Glycine Derivatives
doi 10.1021/ol062126s.s002
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Polycyclic Indoline Derivatives by Dearomatizing Anionic Cyclization of Indole and Tryptamine-Derived Ureas
Organic Letters
Biochemistry
Organic Chemistry
Theoretical Chemistry
Physical
Highly Regio- And Stereoselective Synthesis of Indene Derivatives via Electrophilic Cyclization
Catalyst-Free and Stereoselective Synthesis of N,n-Bicyclic Pyrazolidinone Derivatives
Synthesis
Organic Chemistry
Catalysis
N-BuLi-Initiated Ring-Opening Cyclization of Cyclopropene Derivatives
Synfacts
A NOVEL METHOD FOR THE STEREOSELECTIVE SYNTHESIS OF Β-Aminoacid DERIVATIVES VIA TIN(II) CARBOXYLIC THIOESTER ENOLATES
Chemistry Letters
Chemistry
Stereoselective Acetate Aldol Reactions From Metal Enolates
Synthesis
Organic Chemistry
Catalysis
Separations of Enantiomeric Derivatives of Amines and Amino Acids by Adsorption Chromatography.
Amino Acids and Peptides. III. Synthesis of Some Glycine-Oligopeptides by Way of Pentachlorophenyl Esters
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
Inhibition of the Growth of Hemadsorption 2 Virus by Three Acyl Derivatives of Amino Acids
Antimicrobial Agents and Chemotherapy
Infectious Diseases
Pharmacology