Journal article

Synthesis of the bicyclic dienone core of the antitumor agent ottelione B.

Abstract:: The intramolecular Diels-Alder adduct 12 was converted via dimesylate 20 into dienone 7, which represents the unusual, and apparently quite stable, core of the antitumor agent ottelione B (1).

Publication status:: Published

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APA Style

Clive, D., & Fletcher, S. (2002). Synthesis of the bicyclic dienone core of the antitumor agent ottelione B. Chemical Communications, 8(17), 1940–1941.

MLA Style

Clive, D, and S Fletcher. “Synthesis of the Bicyclic Dienone Core of the Antitumor Agent Ottelione B.” Chemical Communications, vol. 8, no. 17, 2002, pp. 1940–41.

Chicago Style

Clive, D, and S Fletcher. 2002. “Synthesis of the Bicyclic Dienone Core of the Antitumor Agent Ottelione B.” Chemical Communications 8 (17): 1940–41.
Print

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Publisher copy:: 10.1039/b205753k

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:: 8
Issue:: 17
Pages:: 1940-1941
Publication date:: 2002-09-01
DOI:: 10.1039/b205753k
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Keywords:: Antineoplastic Agents, Phytogenic

Cyclohexanones

Molecular Structure
Pubs id:: pubs:117854
UUID:: uuid:1a32b379-2f60-4c38-a79e-63471cde7527
Local pid:: pubs:117854
Source identifiers:: 117854
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_1a32b3792f604c38a79e63471cde7527

Terms of use

Copyright date:: 2002

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

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