Journal article

Synthesis of (-)-(Z)-deoxypukalide.

Abstract:: (Chemical Equation Presented) Closing the deal: A ring-closing metathesis (RCM)/aromatization protocol, followed by a regioselective Negishi cross-coupling reaction and macrolactonization, with subsequent RCM mediate the synthesis of (-)-(Z)-deoxypukalide in 12 linear steps and 15% overall yield (see retrosynthesis; TBS=tert-butyldimethylsilyl, TIPS=triisopropylsilyl). © 2008 Wiley-VCH Verlag GmbH and Co. KGaA.

Publication status:: Published

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APA Style

Donohoe, T., Ironmonger, A., & Kershaw, N. (2008). Synthesis of (-)-(Z)-deoxypukalide. Angewandte Chemie (International Ed. in English), 47(38), 7314–7316.

MLA Style

Donohoe, T., et al. “Synthesis of (-)-(Z)-Deoxypukalide.” Angewandte Chemie (International Ed. in English), vol. 47, no. 38, 2008, pp. 7314–16.

Chicago Style

Donohoe, T, A Ironmonger, and N Kershaw. 2008. “Synthesis of (-)-(Z)-Deoxypukalide.” Angewandte Chemie (International Ed. in English) 47 (38): 7314–16.
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Publisher copy:: 10.1002/anie.200802703

Authors

+ Donohoe, T More by this author

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

+ Ironmonger, A More by this author

Role:: Author

+ Kershaw, N More by this author

Role:: Author

Journal:: Angewandte Chemie (International ed. in English) More from this journal
Volume:: 47
Issue:: 38
Pages:: 7314-7316
Publication date:: 2008-01-01
DOI:: 10.1002/anie.200802703
EISSN:: 1521-3773
ISSN:: 1433-7851

Language:: English
Keywords:: Furans

4-Butyrolactone

Anthozoa

Bridged Compounds

Biological Agents

Animals
Pubs id:: pubs:34346
UUID:: uuid:8001c0eb-9ea8-4108-a42a-0fa410eaf70c
Local pid:: pubs:34346
Source identifiers:: 34346
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2008

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

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