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author:

Chen, T. (Chen, T..) [1] | Wu, W. (Wu, W..) [2] | Weng, Z. (Weng, Z..) [3]

Indexed by:

Scopus

Abstract:

A visible-light photoredox catalyzed reaction of enynones with 2,2,2-trifluoroacetamide to access polysubstituted furfuryl trifluoroacetamide derivatives under mild reaction conditions is reported. This transformation proceeds through the furan-substituted carbene intermediate, which subsequently undergoes an intermocular trapping process by 2,2,2-trifluoroacetamide to produce the desired furfuryl trifluoroacetamides. © 2019 Elsevier Ltd

Keyword:

Cyclization; Enynones; Fluorine; Furan-substituted carbene; Photoredox-catalyzed; Trifluoroacetamide

Community:

  • [ 1 ] [Chen, T.]Fujian Provincial Key Laboratory of Electrochemical Energy Storage Materials, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 2 ] [Wu, W.]Fujian Provincial Key Laboratory of Electrochemical Energy Storage Materials, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 3 ] [Weng, Z.]Fujian Provincial Key Laboratory of Electrochemical Energy Storage Materials, College of Chemistry, Fuzhou University, Fuzhou, 350108, China

Reprint 's Address:

  • [Weng, Z.]Fujian Provincial Key Laboratory of Electrochemical Energy Storage Materials, College of Chemistry, Fuzhou UniversityChina

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Source :

Tetrahedron

ISSN: 0040-4020

Year: 2019

Issue: 51

Volume: 75

2 . 2 3 3

JCR@2019

2 . 1 0 0

JCR@2023

ESI HC Threshold:184

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: 2

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