Synlett 2016; 27(04): 555-558
DOI: 10.1055/s-0035-1560546
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© Georg Thieme Verlag Stuttgart · New York

Enantioselective Addition of Thiols to ortho-Quinone Methides Catalyzed by Chiral Phosphoric Acids

Zengwei Lai
Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR, P. R. of China   eMail: sunjw@ust.hk
,
Jianwei Sun*
Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR, P. R. of China   eMail: sunjw@ust.hk
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Publikationsverlauf

Received: 09. September 2015

Accepted after revision: 04. November 2015

Publikationsdatum:
07. Dezember 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.

Supporting Information