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Synthesis 2019; 51(06): 1391-1398
DOI: 10.1055/s-0037-1610337
DOI: 10.1055/s-0037-1610337
paper
Asymmetric Synthesis of 2,2-Disubstituted Benzofuranones through an Organocatalytic Alkylation with Nitroallylic Acetates
Further Information
Publication History
Received: 09 November 2018
Accepted: 09 November 2018
Publication Date:
30 November 2018 (online)

Abstract
The asymmetric allylic alkylation of benzofuran-3(2H)-ones with nitroallylic acetates has been achieved employing a bifunctional thiourea organocatalyst via SN2′ substitution. A series of 2,2-disubstituted benzofuranones bearing adjacent tetrasubstituted and tertiary stereocenters have been synthesized with moderate to good yields and very good stereoselectivities.
Key words
allylic alkylation - benzofuranones - nitroallylic acetates - organocatalysis - asymmetric synthesisSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0037-1610337.
- Supporting Information
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For a review, see:
For selected examples, see:
For selected reviews on asymmetric allylic alkylations, see: