Journal article

Synthesis of the anti-trypanosomal agent (±)-hydroxyanthecotulide by Cr(ii)-catalysed allylation and Meyer-Schuster rearrangement.

Abstract:: The first synthesis of the bioactive sesquiterpene lactone hydroxyanthecotulide is achieved in 7 steps, involving a stereocontrolled Cr(ii)-catalysed reaction of 3-(bromomethyl)furan-2(5H)-one with enynal 9 and a mild Au(i)-catalysed Meyer-Schuster rearrangement.

Publication status:: Published

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APA Style

Hodgson, D., Talbot, E., & Clark, B. (2012). Synthesis of the anti-trypanosomal agent (±)-hydroxyanthecotulide by Cr(ii)-catalysed allylation and Meyer-Schuster rearrangement. Chemical Communications, 48(51), 6349–6350.

MLA Style

Hodgson, D., et al. “Synthesis of the Anti-Trypanosomal Agent (±)-Hydroxyanthecotulide by Cr(Ii)-Catalysed Allylation and Meyer-Schuster Rearrangement.” Chemical Communications, vol. 48, no. 51, 2012, pp. 6349–50.

Chicago Style

Hodgson, D, E Talbot, and B Clark. 2012. “Synthesis of the Anti-Trypanosomal Agent (±)-Hydroxyanthecotulide by Cr(Ii)-Catalysed Allylation and Meyer-Schuster Rearrangement.” Chemical Communications 48 (51): 6349–50.
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Publisher copy:: 10.1039/c2cc32283h

Authors

+ Hodgson, D More by this author

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

+ Talbot, E More by this author

Role:: Author

+ Clark, B More by this author

Role:: Author

Journal:: Chemical Communications More from this journal
Volume:: 48
Issue:: 51
Pages:: 6349-6350
Publication date:: 2012-05-01
DOI:: 10.1039/c2cc32283h
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Pubs id:: pubs:332004
UUID:: uuid:939e07eb-819f-461c-b43a-a72f0fea4432
Local pid:: pubs:332004
Source identifiers:: 332004
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2012

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

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