4.6 Article

Aryl acrylonitriles synthesis enabled by palladium-catalyzed α-alkenylation of arylacetonitriles with vinyl halides/triflates

期刊

FRONTIERS IN CHEMISTRY
卷 10, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fchem.2022.1091566

关键词

arylacetonitrile; palladium catalysis; alkenylation; isomerization; aryl acrylonitrile

资金

  1. National Key R&D Program of China [2019YFE0109200]
  2. NSFC [21662043]
  3. NSF of Yunnan [202207AA110007, 202207AB110002]
  4. Yunnan Science and Technology Department [2019FY003010]
  5. Ling-Jun Scholars Yunnan Province [202005AB160003]
  6. Program for Xingdian Talents (Yun-Ling Scholars)
  7. IRTSTYN
  8. Yunnan University [2019FY003010]

向作者/读者索取更多资源

In this study, an efficient method for synthesizing aryl acrylonitrile derivatives was developed using a Palladium/NIXANTPHOS-based catalyst system. The method demonstrated high yields and synthetic versatility for various substitutions and functionalizations.
Aryl acrylonitriles are an important subclass of acrylonitriles in the medicinal chemistry and pharmaceutical industry. Herein, an efficient synthesis of aryl acrylonitrile derivatives using a Palladium/NIXANTPHOS-based catalyst system was developed. This approach furnishes a variety of substituted and functionalized aryl acrylonitriles (up to 95% yield). The scalability of the transformation and the synthetic versatility of aryl acrylonitrile were demonstrated.

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