Literature DB >> 26750998

Chiral Frustrated Lewis Pairs Catalyzed Highly Enantioselective Hydrosilylations of 1,2-Dicarbonyl Compounds.

Xiaoyu Ren1, Haifeng Du1.   

Abstract

A highly enantioselective hydrosilylation of 1,2-dicarbonyl compounds was successfully realized for the first time utilizing the combination of tricyclohexylphosphine and chiral alkenylborane derived in situ from diyne as a frustrated Lewis pair catalyst. A variety of optically active α-hydroxy ketones and esters were obtained in 52-98% yields with 86-99% ee's.

Entities:  

Year:  2016        PMID: 26750998     DOI: 10.1021/jacs.5b13104

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Halogenated triphenylgallium and -indium in frustrated Lewis pair activations and hydrogenation catalysis.

Authors:  Maotong Xu; Josephine Possart; Alexander E Waked; Julie Roy; Werner Uhl; Douglas W Stephan
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2017-08-28       Impact factor: 4.226

2.  Investigation on the Synthesis, Application and Structural Features of Heteroaryl 1,2-Diketones.

Authors:  Robert J Wehrle; Alexander Rosen; Thu Vu Nguyen; Kalyn Koons; Eric Jump; Mason Bullard; Natalie Wehrle; Adam Stockfish; Patrick M Hare; Abdurrahman Atesin; Tülay A Ateşin; Lili Ma
Journal:  ACS Omega       Date:  2022-07-20
  2 in total

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