Literature DB >> 21174471

A highly diastereo- and enantioselective copper(I)-catalyzed Henry reaction using a bis(sulfonamide)-diamine ligand.

Wei Jin1, Xincheng Li, Boshun Wan.   

Abstract

A series of bis(sulfonamide)-diamine (BSDA) ligands were synthesized from commercially available chiral α-amino alcohols and diamines. The chiral BSDA ligand 3a, coordinated with Cu(I), catalyzes the enantioselective Henry reaction with excellent enantioselectivity (up to 99%). Moreover, with the assistance of pyridine, a CuBr-3a system promotes the diastereoselective Henry reaction with various aldehyde substrates and gives the corresponding syn-selective adduct with up to a 99% yield and 32.3:1 syn/anti selectivity. The enantiomeric excess of the syn adduct was 97%.

Entities:  

Year:  2010        PMID: 21174471     DOI: 10.1021/jo101932a

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


  2 in total

1.  Enantioselective synthesis of α-oxy amides via Umpolung amide synthesis.

Authors:  Matthew W Leighty; Bo Shen; Jeffrey N Johnston
Journal:  J Am Chem Soc       Date:  2012-09-11       Impact factor: 15.419

Review 2.  Asymmetric catalysis in direct nitromethane-free Henry reactions.

Authors:  Lin Dong; Fen-Er Chen
Journal:  RSC Adv       Date:  2020-01-13       Impact factor: 4.036

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.