2 edition of Biological and mechanistic aspects of 1, 3-dipolar cycloadditions of X=Y-ZH systems. found in the catalog.
Biological and mechanistic aspects of 1, 3-dipolar cycloadditions of X=Y-ZH systems.
William Paul Armstrong
Written in English
Thesis (Ph. D.)--The Queen"s University of Belfast, 1987.
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Buy Biological and mechanistic aspects of 1, 3-dipolar cycloadditions of X=Y-ZH systems by William Paul Armstrong (ISBN:) from Amazon's Book Store. Everyday low Author: William Paul Armstrong. Novel 7-methylenepyrrolo[1,2-c]pyrimidin-1(5H)-ones 11a-c were synthesized from commercially available orotic acid (6).
1,3-Dipolar cycloadditions of mesitonitrile oxide to the exocyclic double. Different multicomponent 1,3-dipolar cycloadditions (1,3-DC) of cyclic α-amino acid derivatives with aldehydes and dipolarophiles have been described as efficient and simple methodologies for the.
X = CHZ, R =Me X=Y-ZH Systems as potential 1,3-dipoles-XXXIH We examined the behaviour of the related oxime (32a) with benzyl acrylate in boiling xylene The tandem process, which is presumed to proceed via nitrone (27c) furnished a 3 1 5 2 mixture of (28c), (29c), (30c) and (31c) Preparative t I c of the mixture afforded pure samples of Cited by: Tetrahedron Vol.
47, No. 38, pp.l91 $+ Printed in Great Britain Pergamon Prcss p X=Y-ZH Systems as Potential 1,3-Dipoles. Part ,2 Generation of Nitrones from Oximes. Tandem Michael Addition 1,3-Dipolar Cycloaddition Reactions. Class 2 Processes Utilising Bifunctional Michael Acceptor-Dipolarophile by: Read "X=Y–ZH system as potential 1,3-dipoles.
Part Cascade 1,3-azaprotio cyclotransfer–1,3-dipolar cycloaddition (1,3-APT–1,3-DC) reactions of benzobicyclo()nonenone oxime, Tetrahedron" on DeepDyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.
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