- 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
- Publisher copy:
- 10.1021/ol202000w
-
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- Journal:
- Organic letters
- Volume:
- 13
- Issue:
- 19
- Pages:
- 5132-5135
- Publication date:
- 2011-10-05
- DOI:
- EISSN:
-
1523-7052
- ISSN:
-
1523-7060
- URN:
-
uuid:89580c4d-b77c-42ba-b72b-7a4dd1195d06
- Source identifiers:
-
175187
- Local pid:
- pubs:175187
- Language:
- English
- Keywords:
- Copyright date:
- 2011
Journal article
Expedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy.
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