4.4 Article

Synthesis of 2,3-Dihydrotryptamines from Amide Solvents and Acyclic Materials through Metal-Free Amidoalkylarylation of Unactivated Alkenes

期刊

SYNLETT
卷 30, 期 11, 页码 1329-1333

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0037-1611825

关键词

amides; cross-coupling; cyclization; green chemistry; radical reaction; tandem reaction

资金

  1. National Natural Science Foundation of China [21702083]
  2. Program for Innovative Research Team (in Science and Technology) in Universities of Yunnan Province
  3. Yunnan Ten Thousand Talent Program for Young Top-Notch Talents
  4. Science Foundation Project of Harbin University of Commerce [18XN067]

向作者/读者索取更多资源

The first synthesis of 2,3-dihydrotryptamines from acyclic materials and an exo -selective amidoalkylation/cyclization cascade of N -allyl anilines through alpha-C(sp (3) )-H functionalization of simple amides across unactivated alkenes are presented. This reaction proceeds in mixed aqueous media and under metal-free conditions and features a broad substrate scope and a simple operation.

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