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Journal article

Expedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy.

Abstract:
An efficient, robust, and scalable strategy to access the functionalized core of calyciphylline A-type alkaloids has been developed starting from commercially available 3-methylanisole. Key features of this approach are an intramolecular Michael addition/allylation sequence and a ring-closing metathesis step.
Publication status:
Published

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Publisher copy:
10.1021/ol202000w

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
Journal:
Organic letters
Volume:
13
Issue:
19
Pages:
5132-5135
Publication date:
2011-10-01
DOI:
EISSN:
1523-7052
ISSN:
1523-7060
Source identifiers:
175187
Language:
English
Keywords:
Pubs id:
pubs:175187
UUID:
uuid:89580c4d-b77c-42ba-b72b-7a4dd1195d06
Local pid:
pubs:175187
Deposit date:
2012-12-19

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