Journal article

A total synthesis of (+)-Goniodiol using an anomeric oxygen-to-carbon rearrangement

Abstract:: A new route to (+)-Goniodiol 1, a potent and selective cytotoxin, is described, using a diastereoselective oxygen-to-carbon rearrangement of an anomerically linked silyl enol ether as the key step.

Publication status:: Published

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APA Style

Dixon, D., Ley, S., & Tate, E. (1998). A total synthesis of (+)-Goniodiol using an anomeric oxygen-to-carbon rearrangement. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 19, 3125–3126.

MLA Style

Dixon, D., et al. “A Total Synthesis of (+)-Goniodiol Using an Anomeric Oxygen-to-Carbon Rearrangement.” JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, no. 19, 1998, pp. 3125–26.

Chicago Style

Dixon, D, S Ley, and E Tate. 1998. “A Total Synthesis of (+)-Goniodiol Using an Anomeric Oxygen-to-Carbon Rearrangement.” JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, no. 19: 3125–26.
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Publisher copy:: 10.1039/a806584e

Authors

+ Dixon, D More by this author

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

+ Ley, S More by this author

Role:: Author

+ Tate, E More by this author

Role:: Author

Journal:: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 More from this journal
Issue:: 19
Pages:: 3125-3126
Publication date:: 1998-10-07
DOI:: 10.1039/a806584e
EISSN:: 1364-5463
ISSN:: 0300-922X

Language:: English
Pubs id:: pubs:52115
UUID:: uuid:54e99f1d-34cb-4a88-baa4-294197ca1af9
Local pid:: pubs:52115
Source identifiers:: 52115
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 1998

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

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