Literature DB >> 28759226

Method for Highly Enantioselective Ligation of Two Chiral C(sp3) Stereocenters.

Eswar Bhimireddy1, E J Corey1.   

Abstract

A method is described for the joining of two α-lithiated C(sp3) stereocenters efficiently and with retention of configuration. The key step involves the effective removal of two electrons from a chiral organocuprate R2CuLi, by i-propyl 2,4-dinitrobenzoate to form a Cu(III) complex that undergoes at -90 °C accelerated reductive elimination enantioselectively and exclusively without the formation of free radicals.

Entities:  

Year:  2017        PMID: 28759226     DOI: 10.1021/jacs.7b07366

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


  1 in total

1.  Asymmetric 1,2-Carbamoyl Rearrangement of Lithiated Chiral Oxazolidine Carbamates and Diastereoselective Synthesis of α-Hydroxy Amides.

Authors:  Arun K Ghosh; Amartyo J Basu; Che-Sheng Hsu; Monika Yadav
Journal:  Chemistry       Date:  2022-06-14       Impact factor: 5.020

  1 in total

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