APPLICATION OF 7-ENDO, 8-ENDO AND 9-ENDO RADICAL CYCLIZATIONS TO THE SYNTHESIS OF CONFORMATIONALLY CONSTRAINED AMINO-ACIDS AND COMPARISON WITH THE CORRESPONDING HECK REACTIONS

Citation
Se. Gibson et al., APPLICATION OF 7-ENDO, 8-ENDO AND 9-ENDO RADICAL CYCLIZATIONS TO THE SYNTHESIS OF CONFORMATIONALLY CONSTRAINED AMINO-ACIDS AND COMPARISON WITH THE CORRESPONDING HECK REACTIONS, Chemical communications, (6), 1997, pp. 637-638
Citations number
21
Categorie Soggetti
Chemistry
Journal title
ISSN journal
13597345
Issue
6
Year of publication
1997
Pages
637 - 638
Database
ISI
SICI code
1359-7345(1997):6<637:AO78A9>2.0.ZU;2-5
Abstract
Radical cyclisation of substrates 1a-c proceeds smoothly to give seven -, eight- and nine-membered rings 3a-c in 73, 71 and 52% yield respect ively; comparison of these results with those obtained using the intra molecular Heck reactions suggests that the two cyclisation methods pro vide complementary approaches to medium-sized rings.