Literature DB >> 22124420

Copper(I) catalyzed asymmetric 1,2-addition of Grignard reagents to α-methyl substituted α,β-unsaturated ketones.

Ashoka V R Madduri1, Adriaan J Minnaard, Syuzanna R Harutyunyan.   

Abstract

The first catalytic enantioselective 1,2-addition of Grignard reagents to ketones is presented. This additive-free copper(I) catalyzed 1,2-addition provides chiral allylic tertiary alcohols with an er of up to 98:2 and excellent yields due to the complete shift of overwhelming 1,4-selectivity of copper(I)-catalysts towards 1,2-selectivity in the addition reaction to enones. This journal is © The Royal Society of Chemistry 2012

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22124420     DOI: 10.1039/c1cc16725a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Asymmetric addition of Grignard reagents to ketones: culmination of the ligand-mediated methodology allows modular construction of chiral tertiary alcohols.

Authors:  Claudio Monasterolo; Ryan O'Gara; Saranna E Kavanagh; Sadbh E Byrne; Bartosz Bieszczad; Orla Murray; Michael Wiesinger; Rebecca A Lynch; Kirill Nikitin; Declan G Gilheany
Journal:  Chem Sci       Date:  2022-04-20       Impact factor: 9.969

2.  Catalytic Enantioselective Addition of Organozirconium Reagents to Aldehydes.

Authors:  Ricard Solà; Marcos Veguillas; María José González-Soria; Nicholas Carter; M Angeles Fernández-Ibáñez; Beatriz Maciá
Journal:  Molecules       Date:  2018-04-20       Impact factor: 4.411

3.  Stereospecific Asymmetric Synthesis of Tertiary Allylic Alcohol Derivatives by Catalytic [2,3]-Meisenheimer Rearrangements.

Authors:  Xin Yu; Nick Wannenmacher; René Peters
Journal:  Angew Chem Int Ed Engl       Date:  2020-04-30       Impact factor: 15.336

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.