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author:

Zheng, H. (Zheng, H..) [1] | Huang, Y. (Huang, Y..) [2] | Weng, Z. (Weng, Z..) [3]

Indexed by:

Scopus

Abstract:

With regard to the high lipophilicity of the trifluoromethylthio group (CF 3 S-), there is a growing interest in the development of efficient methods for the incorporation of CF 3 S moiety onto organic molecules. In this review, recent advances in trifluoromethylthiolation using nucleophilic trifluoromethylthiolating reagents are discussed, highlighting some of the most intriguing examples of the synthesis of trifluoromethylthio-containing compounds using novel reagents. © 2016 Elsevier Ltd. All rights reserved.

Keyword:

Nucleophilic; Reagent; Trifluoromethyl thioethers; Trifluoromethylthiolation

Community:

  • [ 1 ] [Zheng, H.]College of Chemistry and Chemical Engineering, Fuzhou University, Fuzhou, 350108, China
  • [ 2 ] [Huang, Y.]College of Chemistry and Chemical Engineering, Fuzhou University, Fuzhou, 350108, China
  • [ 3 ] [Weng, Z.]College of Chemistry and Chemical Engineering, Fuzhou University, Fuzhou, 350108, China

Reprint 's Address:

  • [Weng, Z.]College of Chemistry and Chemical Engineering, Fuzhou UniversityChina

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Source :

Tetrahedron Letters

ISSN: 0040-4039

Year: 2016

Issue: 13

Volume: 57

Page: 1397-1409

2 . 1 9 3

JCR@2016

1 . 5 0 0

JCR@2023

ESI HC Threshold:235

JCR Journal Grade:2

CAS Journal Grade:3

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count: 143

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 1

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