Literature DB >> 19798719

Organocatalytic asymmetric aza-Michael additions.

Dieter Enders1, Chuan Wang, Jens X Liebich.   

Abstract

The catalytic aza-Michael addition is an important reaction within synthetic organic chemistry, given the significance of the biologically and synthetically interesting products, such as beta-amino acids and beta-lactams. In the last decade organocatalysis emerged as a powerful tool in asymmetric synthesis and had a large impact on the development of asymmetric and catalytic conjugate additions of nitrogen nucleophiles to Michael acceptors. In this review a first summary of the recent rapid progress of asymmetric organocatalyzed aza-Michael reactions is presented.

Entities:  

Year:  2009        PMID: 19798719     DOI: 10.1002/chem.200902236

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  28 in total

1.  Highly enantioselective catalytic synthesis of functionalized chiral diazoacetoacetates.

Authors:  Xinfang Xu; Wen-Hao Hu; Michael P Doyle
Journal:  Angew Chem Int Ed Engl       Date:  2011-05-31       Impact factor: 15.336

Review 2.  Recent advances in C-heteroatom bond forming by asymmetric Michael addition.

Authors:  Majid M Heravi; Parvin Hajiabbasi
Journal:  Mol Divers       Date:  2013-12-31       Impact factor: 2.943

3.  Bifunctional cinchona alkaloid-squaramide-catalyzed highly enantioselective aza-Michael addition of indolines to α,β-unsaturated ketones.

Authors:  Arun K Ghosh; Bing Zhou
Journal:  Tetrahedron Lett       Date:  2013-07-03       Impact factor: 2.415

4.  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

5.  Multifunctional monomer acts as co-initiator and crosslinker to provide autonomous strengthening with enhanced hydrolytic stability in dental adhesives.

Authors:  Linyong Song; Rizacan Sarikaya; Qiang Ye; Anil Misra; Candan Tamerler; Paulette Spencer
Journal:  Dent Mater       Date:  2019-12-03       Impact factor: 5.304

6.  Stereoselective synthesis of chromane derivatives via a domino reaction catalyzed by modularly designed organocatalysts.

Authors:  Satish Jakkampudi; Ramarao Parella; John C-G Zhao
Journal:  Org Biomol Chem       Date:  2018-12-19       Impact factor: 3.876

7.  Formation and Repair of an Interstrand DNA Cross-Link Arising from a Common Endogenous Lesion.

Authors:  Kurt Housh; Jay S Jha; Zhiyu Yang; Tuhin Haldar; Kevin M Johnson; Jiekai Yin; Yinsheng Wang; Kent S Gates
Journal:  J Am Chem Soc       Date:  2021-09-13       Impact factor: 15.419

8.  A Selenourea-Thiourea Brønsted Acid Catalyst Facilitates Asymmetric Conjugate Additions of Amines to α,β-Unsaturated Esters.

Authors:  Yingfu Lin; William J Hirschi; Anuj Kunadia; Anirudra Paul; Ion Ghiviriga; Khalil A Abboud; Rachael W Karugu; Mathew J Vetticatt; Jennifer S Hirschi; Daniel Seidel
Journal:  J Am Chem Soc       Date:  2020-03-11       Impact factor: 15.419

9.  An Asymmetric Organocatalytic Quadruple Cascade to Tetraaryl-Substituted 2-Azabicyclo[3.3.0]octadienones.

Authors:  Céline Joie; Kristina Deckers; Gerhard Raabe; Dieter Enders
Journal:  Synthesis (Stuttg)       Date:  2014-06-01       Impact factor: 3.157

10.  Organocatalytic Asymmetric Synthesis of Functionalized 1,3,5-Triarylpyrrolidin-2-ones via an Aza-Michael/Aldol Domino Reaction.

Authors:  Céline Joie; Kristina Deckers; Dieter Enders
Journal:  Synthesis (Stuttg)       Date:  2014-03-01       Impact factor: 3.157

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.