Issue 80, 2018

Diastereoselective synthesis of 1,3-disubstituted isoindolines and sultams via bronsted acid catalysis

Abstract

The bis(trifluoromethane)sulfonimide (Tf2NH) catalyzed intramolecular hydroamidation of terminal alkynes is reported. The combination of Et3SiH and Tf2NH provides cis-1,3-disubstituted isoindolines and sultams in high yield (up to 98%) and high diastereoselectivity (up to 99 : 1 d.r.).

Graphical abstract: Diastereoselective synthesis of 1,3-disubstituted isoindolines and sultams via bronsted acid catalysis

Associated articles

Supplementary files

Article information

Article type
Communication
Submitted
20 Jun 2018
Accepted
07 Sep 2018
First published
11 Sep 2018

Chem. Commun., 2018,54, 11292-11295

Author version available

Diastereoselective synthesis of 1,3-disubstituted isoindolines and sultams via bronsted acid catalysis

Y. Tao and S. R. Gilbertson, Chem. Commun., 2018, 54, 11292 DOI: 10.1039/C8CC04946G

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