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Tris(2,4,6-trifluorophenyl)borane: An Efficient Hydroboration Catalyst.

ABSTRACT: The metal-free catalyst tris(2,4,6-trifluorophenyl)borane has demonstrated its extensive applications in the 1,2-hydroboration of numerous unsaturated reagents, namely alkynes, aldehydes and imines, consisting of a wide array of electron-withdrawing and donating functionalities. A range of over 50?borylated products are reported, with many reactions proceeding with low catalyst loading under ambient conditions. These pinacol boronate esters, in the case of aldehydes and imines, can be readily hydrolyzed to leave the respective alcohol and amine, whereas alkynyl substrates result in vinyl boranes. This is of great synthetic use to the organic chemist.

SUBMITTER: Lawson JR

PROVIDER: S-EPMC5577513 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature

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Tris(2,4,6-trifluorophenyl)borane: An Efficient Hydroboration Catalyst.

Lawson James R JR Wilkins Lewis C LC Melen Rebecca L RL

Chemistry (Weinheim an der Bergstrasse, Germany) 20170727 46

The metal-free catalyst tris(2,4,6-trifluorophenyl)borane has demonstrated its extensive applications in the 1,2-hydroboration of numerous unsaturated reagents, namely alkynes, aldehydes and imines, consisting of a wide array of electron-withdrawing and donating functionalities. A range of over 50 borylated products are reported, with many reactions proceeding with low catalyst loading under ambient conditions. These pinacol boronate esters, in the case of aldehydes and imines, can be readily hy ...[more]

PMID: 28686789

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