[3+2] cycloaddition reactions: a simple entry to the 1-aza-2-oxo-3,4,5,6-tetrahydroxybicyclo[3.3.0]octane ring system
Metadata of CSIR Papers
View Archive Info| Field | Value | |
| Title |
[3+2] cycloaddition reactions: a simple entry to the 1-aza-2-oxo-3,4,5,6-tetrahydroxybicyclo[3.3.0]octane ring system
|
|
| Creator |
Roy, A
Roy, BG Achari, B Mandal, SB |
|
| Subject |
Chemistry, Organic
|
|
| Description |
The [3+2] intramolecular nitrone cycloaddition (INC) reaction on appropriately designed olefinic nitrones derived from D-glucose, having the nitrone at C-1 and alpha, beta-unsaturated ester functionalities at C-5 of the sugar backbone, afforded the isoxazolidine fused carbocycles 11-13, which were subsequently transformed into the chiral, tetrahydroxylated cis-azabicyclo[3.3.0]octanones 14-18 in good yields. (C) 2004 Elsevier Ltd. All rights reserved.
|
|
| Publisher |
PERGAMON-ELSEVIER SCIENCE LTDOXFORDTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
|
|
| Date |
2011-09-20T12:11:37Z
2011-09-20T12:11:37Z 2004 |
|
| Type |
Article
|
|
| Identifier |
TETRAHEDRON LETTERS
0040-4039 http://hdl.handle.net/123456789/13907 |
|
| Language |
English
|
|