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The first catalytic asymmetric cycloadditions of imines with an enolisable anhydride†
Sarah A. Cronin,Aarón Gutiérrez Collar,Sivaji Gundala,Claudio Cornaggia,Esther Torrente,Francesco Manoni,Astrid Botte,Brendan Twamley,Stephen J. Connon
Organic & Biomolecular Chemistry Pub Date : 07/06/2016 00:00:00 , DOI:10.1039/C6OB00048G
Abstract

The first catalytic, asymmetric reactions of imines with homophthalic anhydride to form disubstituted 3,4-dihydroisoquinolones are reported. The use of N-mesyl aldimines is key, as more basic imines undergo rapid uncatalysed reactions, while imines possessing larger N-sulphonyl substituents form lactams with lower ee.

Graphical abstract: The first catalytic asymmetric cycloadditions of imines with an enolisable anhydride
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