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Synlett 2016; 27(04): 555-558
DOI: 10.1055/s-0035-1560546
DOI: 10.1055/s-0035-1560546
cluster
Enantioselective Addition of Thiols to ortho-Quinone Methides Catalyzed by Chiral Phosphoric Acids
Further Information
Publication History
Received: 09 September 2015
Accepted after revision: 04 November 2015
Publication Date:
07 December 2015 (online)


Abstract
The first Brønsted acid catalyzed enantioselective addition of thiols to the in situ generated ortho-quinone methides (o-QMs) is described. Complementary to the chiral amine catalyzed approach, the present reaction employs a chiral phosphoric acid as the catalyst. The readily available o-hydroxybenzyl alcohols serve as the atom-economical precursors of o-QMs to react with tritylthiol with moderate to good efficiency and enantioselectivity under mild conditions.
Key words
asymmetric catalysis - quinone methide - organocatalysis - nucleophilic addition - Brønsted acidSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1560546.
- Supporting Information