X=y-ZH compounds as potential 1,3-dipoles. part 44.1 asymmetric 1,3-dipolar cycloaddition reactions of imines and chiral cyclic dipolarophiles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. X=Y−ZH compounds as potential 1,3-dipoles. Part 43. Metal ion catalysed asymmetric 1,3-dipolar cycloaddition reactions of imines and menthyl acrylate
2. X = Y - ZH systems as potential 1,3-dipoles. Part 40. Chiral azomethine ylides from homochiral cyclic α-amino esters. Unusual regiospecific deprotonation of iminium ions.
3. Sequential and cascade 1,3-dipolar cycloaddition-palladium catalysed carbonylation-cyclisation reactions. Diastereospecific and homochiral processes
4. Chiral induction in cycloaddition reactions of azomethine ylides derived from secondary α-amino acids by the decarboxylative route
5. Chiral Co(II) and Mn(II) catalysts for the 1,3-dipolar cycloaddition reactions of azomethine ylides derived from arylidene imines of glycine
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