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1,2 : 3,4-Di-O-isopropylidene-alpha-D-tagatofuranose

Abstract:
The crystal structure of diacetone tagatose, C12H 20O6, establishes the stereochemistry of the anomeric spiroacetal as 1,2:3,4-di-O-isopropylidene-α-D-tagatofuranose. Molecules are linked by O - H⋯O hydrogen bonds [O⋯O = 2.862 (2) Å] to form chains running parallel to the b axis. © 2005 International Union of Crystallography Printed in Great Britain - all rights reserved.
Publication status:
Published

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Publisher copy:
10.1107/S1600536805025092

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Role:
Author


Journal:
ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE More from this journal
Volume:
61
Issue:
9
Pages:
O2891-O2893
Publication date:
2005-09-01
DOI:
EISSN:
1600-5368
ISSN:
1600-5368


Language:
English
Pubs id:
pubs:39667
UUID:
uuid:0558e02d-dbe3-4287-88a7-d141c634b956
Local pid:
pubs:39667
Source identifiers:
39667
Deposit date:
2012-12-19
ARK identifier:

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