Chengcheng Fang , Jie-Qing Ou , Xiaoye Mo , Yingqian Xu , Sifeng Li
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Palladium-catalyzed chemoselective N-monoallylation of aromatic amines with diallylamine through a borrowing hydrogen strategy
A palladium-catalyzed N-monoallylation reaction of aromatic amines with diallylamine at relatively low temperatures has been established for the synthesis of N-monoallylated amines via a borrowing hydrogen strategy. Employing diallylamine as the allylating agent, primary (hetero)aryl amines, N-alkyl secondary (hetero)aryl amines, N,N-diarylamines, and various commercially available aniline-containing pharmaceuticals can be utilized to synthesize N-monoallyl aromatic amines with releasing ammonia as the by-product.
期刊介绍:
Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry.
Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters.
Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.