Journal article

2-C-Hydroxymethyl-2,3-O-isopropyl-idene-3-C-methyl-beta-L-erythrose

Abstract:: The relative configuration of the title compound, C9H16O5, has been firmly established by X-ray crystallographic analysis. The absolute configuration of this sugar was determined by the use of 2-C-methyl-d-ribono-1,4-lactone as the starting material. The structure exists as a hydrogen-bonded network, with each mol-ecule being a donor and an acceptor for two hydrogen bonds. © International Union of Crystallography 2007.

Publication status:: Published

Actions

Email

Email this record

Send the bibliographic details of this record to your email address.

Your Email
Please enter the email address that the record information will be sent to.

-
Your message (optional)
Please add any additional information to be included within the email.
Cite

Cite this record

APA Style

Booth, K., Jenkinson, S., Watkin, D., & Fleet, G. (2007). 2-C-Hydroxymethyl-2,3-O-isopropyl-idene-3-C-methyl-beta-L-erythrose. ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 63(8), O3386–U2312.

MLA Style

Booth, K., et al. “2-C-Hydroxymethyl-2,3-O-Isopropyl-Idene-3-C-Methyl-Beta-L-Erythrose.” ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, vol. 63, no. 8, 2007, pp. O3386–U2312.

Chicago Style

Booth, K, S Jenkinson, D Watkin, and G Fleet. 2007. “2-C-Hydroxymethyl-2,3-O-Isopropyl-Idene-3-C-Methyl-Beta-L-Erythrose.” ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE 63 (8): O3386–U2312.
Share
Print

Access Document

Publisher copy:: 10.1107/S1600536807031522

Authors

+ Booth, K More by this author

Role:: Author

+ Jenkinson, S More by this author

Role:: Author

+ Watkin, D More by this author

Role:: Author

+ Fleet, G More by this author

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:: 63
Issue:: 8
Pages:: O3386-U2312
Publication date:: 2007-08-01
DOI:: 10.1107/S1600536807031522
EISSN:: 1600-5368
ISSN:: 1600-5368

Language:: English
Pubs id:: pubs:288131
UUID:: uuid:02edf99c-215e-441b-bdf9-4b35e3b18560
Local pid:: pubs:288131
Source identifiers:: 288131
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2007

Licence:: Terms and Conditions of Use for Oxford University Research Archive

Views and Downloads

About views and downloads

If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP