A palladium-catalyzed carbo-oxygenation: the bielschowskysin case
- PMID: 23724910
- PMCID: PMC3691719
- DOI: 10.1021/ol401285d
A palladium-catalyzed carbo-oxygenation: the bielschowskysin case
Abstract
An asymmetric synthesis of an advanced tetracyclic intermediate toward the synthesis of bielschowskysin (1) is described. A biomimetic [2 + 2]-photocyclization was used to establish the cyclobutane core of bielschowskysin. Macrocyclization under Heck conditions led to an unprecedented carbo-oxygenation of a 1,1-disubstituted double bond.
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- Farcet J.-B.; Himmelbauer M.; Mulzer J.. Eur. J. Org. Chem. 2013, accepted for publication
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