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Synthesis of carboxylated pyrrolidine derivatives via 1,3-dipolar cycloadditions of homochiral double-stabilised E-azomethine ylids

✍ Scribed by L.M. Harwood; I.A. Lilley


Book ID
103977191
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
218 KB
Volume
6
Category
Article
ISSN
0957-4166

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πŸ“œ SIMILAR VOLUMES


Diastereoselective synthesis of pyrrolid
✍ K. Karthikeyan; R. Senthil Kumar; D. Muralidharan; P.T. Perumal πŸ“‚ Article πŸ“… 2009 πŸ› Elsevier Science 🌐 French βš– 691 KB

1,3-Dipolar cycloaddition of D-glucose-derived azomethine ylides for the synthesis of chiral pyrrolidines accompanied an unexpected 1,2-elimination in the furanose moiety of the products. The C3 0 alkoxy/ hydroxy group of the furanose moiety was invariably eliminated under the reaction conditions. A