Novel synthesis of carbohydrate fused alpha-amino gamma-lactams and glycopeptides by NIS mediated ring opening of donor-acceptor substituted cyclopropanes
Data(s) |
2014
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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 |