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Recent developments in the trifluoromethylation of alkynes.
Chemistry. 2015 May 18; 21(21):7648-61.C

Abstract

In the last few years, the development of versatile methodologies to incorporate trifluoromethyl groups into organic molecules has attracted significant attention in synthetic chemistry. This review gives an overview over the development on the trifluoromethylation of alkynes, which have not been solely discussed before. Formation of diverse C(sp, sp(2) , sp(3))-CF3 bonds are all covered in this review.

Links

Publisher Full Text (DOI)

Authors+Show Affiliations

Gao P
State key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000 (China), Fax: (+86) 931-891-2582.
Song XR
No affiliation info available
Liu XY
No affiliation info available
Liang YM
No affiliation info available

MeSH

AlkynesChemistry Techniques, SyntheticHalogenationHydrocarbons, FluorinatedMethylation

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't
Review

Language

eng

PubMed ID

25737368

Citation

Gao, Pin, et al. "Recent Developments in the Trifluoromethylation of Alkynes." Chemistry (Weinheim an Der Bergstrasse, Germany), vol. 21, no. 21, 2015, pp. 7648-61.
Gao P, Song XR, Liu XY, et al. Recent developments in the trifluoromethylation of alkynes. Chemistry. 2015;21(21):7648-61.
Gao, P., Song, X. R., Liu, X. Y., & Liang, Y. M. (2015). Recent developments in the trifluoromethylation of alkynes. Chemistry (Weinheim an Der Bergstrasse, Germany), 21(21), 7648-61. https://doi.org/10.1002/chem.201406432
Gao P, et al. Recent Developments in the Trifluoromethylation of Alkynes. Chemistry. 2015 May 18;21(21):7648-61. PubMed PMID: 25737368.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Recent developments in the trifluoromethylation of alkynes. AU - Gao,Pin, AU - Song,Xian-Rong, AU - Liu,Xue-Yuan, AU - Liang,Yong-Min, Y1 - 2015/03/03/ PY - 2015/3/5/entrez PY - 2015/3/5/pubmed PY - 2016/1/27/medline KW - alkyne KW - difunctionalization KW - radical reactions KW - synthetic methods KW - trifluoromethylation SP - 7648 EP - 61 JF - Chemistry (Weinheim an der Bergstrasse, Germany) JO - Chemistry VL - 21 IS - 21 N2 - In the last few years, the development of versatile methodologies to incorporate trifluoromethyl groups into organic molecules has attracted significant attention in synthetic chemistry. This review gives an overview over the development on the trifluoromethylation of alkynes, which have not been solely discussed before. Formation of diverse C(sp, sp(2) , sp(3))-CF3 bonds are all covered in this review. SN - 1521-3765 UR - https://www.unboundmedicine.com/medline/citation/25737368/Recent_developments_in_the_trifluoromethylation_of_alkynes_ DB - PRIME DP - Unbound Medicine ER -