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Synthesis 2016; 48(01): 79-84
DOI: 10.1055/s-0035-1560833
DOI: 10.1055/s-0035-1560833
paper
N-Heterocyclic Carbene-Catalyzed Vinylogous Mukaiyama Aldol Reaction of α-Keto Esters and α-Trifluoromethyl Ketones
Further Information
Publication History
Received: 16 August 2015
Accepted after revision: 07 October 2015
Publication Date:
04 November 2015 (online)
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Abstract
N-Heterocyclic carbene (NHC)-catalyzed vinylogous Mukaiyama aldol reaction of ketones was developed. Under the catalysis of 5 mol% NHC, α-keto esters and α-trifluoromethyl ketones reacted with 2-(trimethysilyloxy)furan efficiently to produce γ-substituted butenolides containing adjacent quaternary and tertiary carbon centers in high yields with good diastereoselectivities.
Key words
N-heterocyclic carbene - NHC - vinylogous Mukaiyama aldol reaction - 2-(trimethysilyloxy)furan - butenolideSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1560833.
- Supporting Information
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