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Journal article

2-C-azidomethyl-2-deoxy-3,4-O-isopropylidene-D-ribono-1,5-lactone

Abstract:
X-ray crystallographic analysis firmly establishes the ribo stereochemistry and the unusual boat conformation of the title branched carbon chain lactone, C9H13N3O4, arising from an unexpected rearrangement in the nucleophilic substitution of a trifluoromethanesulfonate. There are two molecules in the asymmetric unit. © 2006 International Union of Crystallography Printed in Great Britain - all rights reserved.
Publication status:
Published

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Publisher copy:
10.1107/S1600536805041632

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


Journal:
ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE More from this journal
Volume:
62
Issue:
1
Pages:
O321-O323
Publication date:
2006-01-01
DOI:
EISSN:
1600-5368
ISSN:
1600-5368


Language:
English
Pubs id:
pubs:39831
UUID:
uuid:0348e4ef-f396-47ca-98b0-d98b2a5fe23c
Local pid:
pubs:39831
Source identifiers:
39831
Deposit date:
2012-12-19
ARK identifier:

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