An easy access to spiroannulated glyco-oxetane, -thietane and -azetane rings: synthesis of spironucleosides
Metadata of CSIR Papers
View Archive Info| Field | Value | |
| Title |
An easy access to spiroannulated glyco-oxetane, -thietane and -azetane rings: synthesis of spironucleosides
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| Creator |
Roy, A
Achari, B Mandal, SB |
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| Subject |
Chemistry, Organic
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| Description |
The key intermediate 11 derived from D-glucose and possessing bis-mesylmethyl (MsO center dot CH2-) functionality at C-4, was used to generate spirocycles 12, 13 and 15 via one-step procedures. The spirocompounds 12 and 13 were subsequently converted into the corresponding spironucleosides 24 and 26 in good yield using Vorbruggen reaction conditions. (c) 2006 Elsevier Ltd. All rights reserved.
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| Publisher |
PERGAMON-ELSEVIER SCIENCE LTDOXFORDTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
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| Date |
2011-09-20T12:12:14Z
2011-09-20T12:12:14Z 2006 |
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| Type |
Article
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| Identifier |
TETRAHEDRON LETTERS
0040-4039 http://hdl.handle.net/123456789/14185 |
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| Language |
English
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