| Literature DB >> 28901769 |
Eric J Alexy1, Scott C Virgil1, Michael D Bartberger2, Brian M Stoltz1.
Abstract
A catalytic, enantioselective decarboxylative allylic alkylation of 4-thiopyranones is reported. The α-quaternary 4-thiopyranones produced are challenging to access by standard enolate alkylation owing to facile ring-opening β-sulfur elimination. In addition, reduction of the carbon-sulfur bonds provides access to elusive acyclic α-quaternary ketones. The alkylated products are obtained in up to 92% yield and 94% enantiomeric excess.Entities:
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Year: 2017 PMID: 28901769 PMCID: PMC5632216 DOI: 10.1021/acs.orglett.7b02354
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005