Literature DB >> 21247143

Catalytic asymmetric aza-Michael-Michael addition cascade: enantioselective synthesis of polysubstituted 4-aminobenzopyrans.

Xu-Fan Wang1, Jing An, Xiao-Xiao Zhang, Fen Tan, Jia-Rong Chen, Wen-Jing Xiao.   

Abstract

A catalytic asymmetric aza-Michael-Michael addition cascade of anilines to nitroolefin enoates in the presence of chiral bifunctional thiourea catalysts has been disclosed. This reaction provides a mild and efficient approach to polysubstituted chiral 4-aminobenzopyrans bearing three consecutive stereocenters in high yields with excellent stereoselectivities.

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Year:  2011        PMID: 21247143     DOI: 10.1021/ol1031188

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Catalyst-free, aza-Michael polymerization of hydrazides: polymerizability, kinetics, and mechanistic origin of an α-effect.

Authors:  Dillon Love; Kangmin Kim; Dylan W Domaille; Olivia Williams; Jeffrey Stansbury; Charles Musgrave; Christopher Bowman
Journal:  Polym Chem       Date:  2019-10-08       Impact factor: 5.582

2.  Plausible Pnicogen Bonding of epi-Cinchonidine as a Chiral Scaffold in Catalysis.

Authors:  Zakir Ullah; Kang Kim; Arramshetti Venkanna; Hye Su Kim; Moon Il Kim; Mi-Hyun Kim
Journal:  Front Chem       Date:  2021-07-06       Impact factor: 5.221

Review 3.  (Thio)urea-mediated synthesis of functionalized six-membered rings with multiple chiral centers.

Authors:  Giorgos Koutoulogenis; Nikolaos Kaplaneris; Christoforos G Kokotos
Journal:  Beilstein J Org Chem       Date:  2016-03-10       Impact factor: 2.883

  3 in total

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