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author:

Rong, M. (Rong, M..) [1] | Huang, R. (Huang, R..) [2] | You, Y. (You, Y..) [3] | Weng, Z. (Weng, Z..) [4]

Indexed by:

Scopus

Abstract:

The copper-mediated trifluoromethylselenolation of propargylic chlorides and allylic bromides is described. This approach provides a wide range of propargylic and allylic trifluoromethyl selenoethers in moderate to good yields. These results open the way to synthesis strategies for various trifluoromethylselenolated compounds. © 2014 Elsevier Ltd. All rights reserved.

Keyword:

Allylic trifluoromethyl selenoethers; Copper; Propargylic trifluoromethyl selenoethers; Trifluoromethylselenolation; Trifluoromethylthiolation

Community:

  • [ 1 ] [Rong, M.]Department of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 2 ] [Huang, R.]Department of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 3 ] [You, Y.]Department of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 4 ] [Weng, Z.]Department of Chemistry, Fuzhou University, Fuzhou, 350108, China

Reprint 's Address:

  • [You, Y.]Department of Chemistry, Fuzhou UniversityChina

Email:

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Source :

Tetrahedron

ISSN: 0040-4020

Year: 2014

Issue: 46

Volume: 70

Page: 8872-8878

2 . 6 4 1

JCR@2014

2 . 1 0 0

JCR@2023

ESI HC Threshold:268

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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