sigma-Ferrier rearrangement of carbohydrate derived vinylcyclopropanes: a facile approach to oxepane analogs


Autoria(s): Ganesh, Venkataraman; Kundu, Taraknath; Chandrasekaran, Srinivasan
Data(s)

2014

Resumo

This article presents our work on the sigma-Ferrier ring-expansion of carbohydrate derived vinylcyclopropanes (VCPs) under electrophilic conditions mediated by chloramine-T and a phase-transfer catalyst. The present work serves as the first example on the studies of the reactivity of carbohydrate VCPs towards the synthesis of densely functionalized oxepane analogues. The work elaborates on a reasonable mechanism for the product formation and our observations on the diastereoselectivity based on control experiments and gas-phase calculations. (C) 2014 Elsevier Ltd. All rights reserved.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/50221/1/tet_70-40_7268_2014.pdf

Ganesh, Venkataraman and Kundu, Taraknath and Chandrasekaran, Srinivasan (2014) sigma-Ferrier rearrangement of carbohydrate derived vinylcyclopropanes: a facile approach to oxepane analogs. In: TETRAHEDRON, 70 (40, SI). pp. 7268-7282.

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

http://dx.doi.org/ 10.1016/j.tet.2014.07.004

http://eprints.iisc.ernet.in/50221/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed