Journal article

Enantioselective total synthesis of (-)-xialenon A.

Abstract:: The first total synthesis of (-)-xialenon A (1) via conjugate allylation of a 1,5-cyclooctadiene-derived bicyclo[3.3.0]octenone 3 and an alpha'-hydroxylation on the more hinderd face of enone 9 using hypervalent iodine chemistry, is described.

Publication status:: Published

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APA Style

Hodgson, D., Galano, J., & Christlieb, M. (2002). Enantioselective total synthesis of (-)-xialenon A. Chemical Communications, 20, 2436–2437.

MLA Style

Hodgson, D., et al. “Enantioselective Total Synthesis of (-)-Xialenon A.” Chemical Communications, no. 20, 2002, pp. 2436–37.

Chicago Style

Hodgson, D, J Galano, and M Christlieb. 2002. “Enantioselective Total Synthesis of (-)-Xialenon A.” Chemical Communications, no. 20: 2436–37.
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Publisher copy:: 10.1039/b208485f

Authors

+ Hodgson, D More by this author

Institution:

University of Oxford

Division:

MPLS

Department:

Chemistry

Sub department:

Organic Chemistry

Role:

Author

+ Galano, J More by this author

Role:

Author

+ Christlieb, M More by this author

Role:

Author

Bibliographic Details

Journal:: Chemical Communications More from this journal
Issue:: 20
Pages:: 2436-2437
Publication date:: 2002-10-01
DOI:: 10.1039/b208485f
EISSN:: 1364-548X
ISSN:: 1359-7345

Item Description

Language:: English
Keywords:: Stereoisomerism

Biological Factors

Hydroxylation

Streptomyces

Alkylation

Cyclooctanes
Pubs id:: pubs:32245
UUID:: uuid:f3e7a0f5-5456-4d96-9a8b-c2028dba6283
Local pid:: pubs:32245
Source identifiers:: 32245
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2002

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

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