Novel synthesis of carbohydrate fused alpha-amino gamma-lactams and glycopeptides by NIS mediated ring opening of donor-acceptor substituted cyclopropanes


Autoria(s): Kishore, Gade; Gautam, Vibha; Chandrasekaran, Srinivasan
Data(s)

2014

Resumo

alpha-Amino gamma-lactams have been synthesized from carbohydrate derived cyclopropanecarboxylates using N-iodosuccinimide (NIS) and NaN3. Cyclopropane ring opening with NIS and NaN3 in different solvents has been studied. Reductive cyclization of the intermediate di-azides leads to the carbohydrate fused alpha-amino gamma-lactam and gamma-lactams. Additionally, the methodology has been successfully extended to the synthesis of a glycopeptide. (C) 2014 Elsevier Ltd. All rights reserved.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/49210/1/car_res_390_1_2014.pdf

Kishore, Gade and Gautam, Vibha and Chandrasekaran, Srinivasan (2014) Novel synthesis of carbohydrate fused alpha-amino gamma-lactams and glycopeptides by NIS mediated ring opening of donor-acceptor substituted cyclopropanes. In: CARBOHYDRATE RESEARCH, 390 . pp. 1-8.

Publicador

ELSEVIER SCI LTD

Relação

http://dx.doi.org/10.1016/j.carres.2014.02.022

http://eprints.iisc.ernet.in/49210/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed