Journal article

Synthesis of (+)-nocardione A--use of formal radical cyclization onto a benzene ring.

Abstract:: Juglone (7) was converted into enone 13; this underwent radical cyclization to afford 15, which was aromatized to 16 and elaborated into (+)-nocardione A (1), the enantiomer of the naturally-occurring tyrosine phosphatase inhibitor (-)-nocardione A (2).

Publication status:: Published

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APA Style

Clive, D., & Fletcher, S. (2003). Synthesis of (+)-nocardione A--use of formal radical cyclization onto a benzene ring. Chemical Communications, 9(19), 2464–2465.

MLA Style

Clive, D., and S. Fletcher. “Synthesis of (+)-Nocardione A--Use of Formal Radical Cyclization onto a Benzene Ring.” Chemical Communications, vol. 9, no. 19, 2003, pp. 2464–65.

Chicago Style

Clive, D, and S Fletcher. 2003. “Synthesis of (+)-Nocardione A--Use of Formal Radical Cyclization onto a Benzene Ring.” Chemical Communications 9 (19): 2464–65.
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Publisher copy:: 10.1039/b307937f

Authors

+ Clive, D More by this author

Role:: Author

+ Fletcher, S More by this author

Role:: Author

Journal:: Chemical Communications More from this journal
Volume:: 9
Issue:: 19
Pages:: 2464-2465
Publication date:: 2003-10-01
DOI:: 10.1039/b307937f
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Keywords:: Cyclization

Furans

Naphthoquinones

Benzene

Molecular Structure
Pubs id:: pubs:117856
UUID:: uuid:9a6162ad-2d65-402d-8ddc-3badaf435417
Local pid:: pubs:117856
Source identifiers:: 117856
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2003

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

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