Affiliation:
1. School of Pharmacy & School of Biological and Food Engineering Changzhou University Changzhou 213164 China
2. Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology School of Petrochemical Engineering Changzhou University Changzhou 213164 China
Abstract
AbstractBenzyl amines were deaminated for the olefination of methyl N‐heteroarenes such as quinolines, benzothiazoles, and quinoxalines catalyzed by 4,6‐dihydroxysalicylic acid with only 1 mol % catalyst loading. A wide range of N‐heteroaryl stilbenoids were synthesized in yields of 42 to 96 % using oxygen (1 atm) as the sole oxidant. 4,6‐dihydroxysalicylic acid not only behaves as an organocatalyst for the oxidation of benzyl amines to the imine intermediates, but also provides an acidic reaction condition for the olefinations. Gram scale reaction and the synthesis of two pharmaceutically relevant conjugated olefins were also successful using this methodology.
Funder
Natural Science Research of Jiangsu Higher Education Institutions of China
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Cited by
1 articles.
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