| Literature DB >> 22228324 |
Abstract
We report the first example of highly enantioselective organocatalytic synthesis of 3-difluoroalkyl substituted 3-hydroxyoxindoles. The total synthesis of the difluoro analogue of convolutamydine E was achieved by this method. This journal is © The Royal Society of Chemistry 2012Entities:
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Year: 2012 PMID: 22228324 DOI: 10.1039/c2cc17140f
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222