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Journal article

2-C-Methyl-D-allono-1,4-lactone

Abstract:
The relative stereochemistry of the compound 2-c-methyl-D-allono-1,4-lactone was established using X ray crystallographic analysis. The absolute stereochemistry was defined by the use of D-ribonolactone as a starting material. All H atoms were observed in a difference electron density map and were refined using slack restraints to optimize their geometry. The crystal structure was made up of layers of strongly hydrogen-bonded molecules, which were found to be lying in the ab plane.
Publication status:
Published

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Publisher copy:
10.1107/S1600536805012328

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:
61
Issue:
5
Pages:
O1472-O1474
Publication date:
2005-05-01
DOI:
EISSN:
1600-5368
ISSN:
1600-5368


Language:
English
Pubs id:
pubs:39520
UUID:
uuid:20d89f30-2103-4c59-ad18-bca5cdf281e8
Local pid:
pubs:39520
Source identifiers:
39520
Deposit date:
2012-12-19

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