Issue 69, 2020

Nickel(ii)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles

Abstract

A nickel(II) catalyzed enantioselective thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles was realized with modified chiral N,N′-dioxide ligands, affording a variety of C3-substituted indole derivatives in high yields (up to 95%) with excellent enantioselectivities (up to 96% ee) under mild reaction conditions. A possible transition state model was proposed based on previous reports and the X-ray crystal structure of the catalyst.

Graphical abstract: Nickel(ii)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles

Supplementary files

Article information

Article type
Communication
Submitted
02 Jul 2020
Accepted
21 Jul 2020
First published
22 Jul 2020

Chem. Commun., 2020,56, 10002-10005

Nickel(II)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles

W. Yang, X. Lin, Y. Zhang, W. Cao, X. Liu and X. Feng, Chem. Commun., 2020, 56, 10002 DOI: 10.1039/D0CC04590J

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