Literature DB >> 10774019

Synthesis of 3-trifluoroethylfurans by palladium-catalyzed cyclization-isomerization of (Z)-2-alkynyl-3-trifluoromethyl allylic alcohols

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Abstract

Hydroiodonation of trifluoromethyl propargylic alcohols 1 regio- and stereoselectively produce (Z)-2-iodo-3-trifluoromethyl allylic alcohols 2. (Z)-2-Alkynyl-3-trifluoromethyl allylic alcohols 5, available through Pd(PPh3)4-mediated coupling of 2 and terminal alkynes 4, cyclize and subsequently isomerize to 3-trifluoroethylfurans 6 upon catalysis under PdCl2(CH3CN)2 in THF at 5-10 degrees C.

Entities:  

Year:  2000        PMID: 10774019     DOI: 10.1021/jo991463u

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

Review 1.  Transition metal-mediated synthesis of monocyclic aromatic heterocycles.

Authors:  Anton V Gulevich; Alexander S Dudnik; Natalia Chernyak; Vladimir Gevorgyan
Journal:  Chem Rev       Date:  2013-01-10       Impact factor: 60.622

2.  Solution-phase synthesis of a highly substituted furan library.

Authors:  Chul-Hee Cho; Feng Shi; Dai-Il Jung; Benjamin Neuenswander; Gerald H Lushington; Richard C Larock
Journal:  ACS Comb Sci       Date:  2012-06-11       Impact factor: 3.784

3.  Regioselective carbon-carbon bond formation of 5,5,5-trifluoro-1-phenylpent-3-en-1-yne.

Authors:  Motoki Naka; Tomoko Kawasaki-Takasuka; Takashi Yamazaki
Journal:  Beilstein J Org Chem       Date:  2013-10-23       Impact factor: 2.883

  3 in total

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