Chiral induction in cycloaddition reactions of azomethine ylides derived from secondary α-amino acids by the decarboxylative route
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Metal ion catalysed asymmetric 1,3-dipolar cycloaddition reactions of imines of α-amino esters
2. Asymmetric 1,3-dipolar cycloadditions of azomethine ylides with a chiral electron-deficient olefinic dipolarophile
3. Decarboxylation of α-amino acids by pyruvic acid and its derivatives. Evidence for azomethine ylides in analogues of pyruvoyl enzymic processes
4. X=Y-ZH compounds as potential 1,3-Dipoles. Part 281,2 the iminium ion route to azomethine ylides. background and reaction of amines with bifunctional ketones.
5. X=Y-ZH compounds as potential 13-dipoles. Part 29. The iminium ion route to azomethine ylides. Reaction of cyclic secondary amines with mono- and bI- functional aldehydes
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3. Recent Advances on Diverse Decarboxylative Reactions of Amino Acids;Advanced Synthesis & Catalysis;2019-02-13
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