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author:

Zhou, Ledan (Zhou, Ledan.) [1] | Liu, Ding (Liu, Ding.) [2] | Huang, Huashan (Huang, Huashan.) [3] | Zhang, Ke (Zhang, Ke.) [4] | Ning, Yingtang (Ning, Yingtang.) [5] | Chen, Fen-Er (Chen, Fen-Er.) [6]

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EI

Abstract:

We report a general approach to highly functionalized (Z)-allylic amines by decarboxylative allylation of vinyloxazolidin-2-ones. This process engages sodium sulfinates as nucleophiles to form a new carbon-sulfur bond, utilizing a palladium catalyst generated from Pd(OAc)2 and diphosphine ligand dpppe. The scope of the protocol is illustrated by the synthesis of 30 representative allylic amines with high regio- and stereoselectivity. Mechanistic studies show that the Z-selectivity of the reaction stems from the formation of a palladacycle intermediate through Pd-N chelation. The synthetic utility of this method was further exemplified by the gram-scale synthesis and subsequent transformations to various compounds. © 2023 The Royal Society of Chemistry

Keyword:

Allylation Amines Catalysts Palladium Palladium compounds Reaction intermediates Sodium Stereoselectivity

Community:

  • [ 1 ] [Zhou, Ledan]College of Chemistry, Fuzhou University, Fuzhou; 350102, China
  • [ 2 ] [Zhou, Ledan]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Fudan University, Shanghai; 200433, China
  • [ 3 ] [Zhou, Ledan]Shanghai Engineering Center of Industrial Catalysis for Chiral Drugs, Shanghai; 200433, China
  • [ 4 ] [Liu, Ding]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Fudan University, Shanghai; 200433, China
  • [ 5 ] [Liu, Ding]Shanghai Engineering Center of Industrial Catalysis for Chiral Drugs, Shanghai; 200433, China
  • [ 6 ] [Huang, Huashan]College of Chemistry, Fuzhou University, Fuzhou; 350102, China
  • [ 7 ] [Huang, Huashan]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Fudan University, Shanghai; 200433, China
  • [ 8 ] [Huang, Huashan]Shanghai Engineering Center of Industrial Catalysis for Chiral Drugs, Shanghai; 200433, China
  • [ 9 ] [Zhang, Ke]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Fudan University, Shanghai; 200433, China
  • [ 10 ] [Zhang, Ke]Shanghai Engineering Center of Industrial Catalysis for Chiral Drugs, Shanghai; 200433, China
  • [ 11 ] [Ning, Yingtang]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Fudan University, Shanghai; 200433, China
  • [ 12 ] [Ning, Yingtang]Shanghai Engineering Center of Industrial Catalysis for Chiral Drugs, Shanghai; 200433, China
  • [ 13 ] [Chen, Fen-Er]College of Chemistry, Fuzhou University, Fuzhou; 350102, China
  • [ 14 ] [Chen, Fen-Er]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Fudan University, Shanghai; 200433, China
  • [ 15 ] [Chen, Fen-Er]Shanghai Engineering Center of Industrial Catalysis for Chiral Drugs, Shanghai; 200433, China

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Source :

Chemical Communications

ISSN: 1359-7345

Year: 2023

Issue: 65

Volume: 59

Page: 9892-9895

4 . 3

JCR@2023

4 . 3 0 0

JCR@2023

JCR Journal Grade:2

CAS Journal Grade:3

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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