Literature DB >> 16468777

Zn(pybox)-complex-catalyzed asymmetric aqueous Mukaiyama-aldol reactions.

Joanna Jankowska1, Jacek Mlynarski.   

Abstract

Catalytic asymmetric aldol reactions in aqueous media have been developed using chiral zinc complex. The aldol products have been obtained in high yields, high diastereocontrol, and good level of enantioselectivity. Various aromatic and alpha,beta-unsaturated aldehydes and silyl enol ethers derived from ketones can be employed in this reaction to provide the aldol adducts in good to high yield. The elaborated catalytic system has been found as selective for aliphatic aldehydes as well.

Entities:  

Year:  2006        PMID: 16468777     DOI: 10.1021/jo0514568

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


  3 in total

1.  Stereoselective synthesis of highly functionalized alpha-diazo-beta-ketoalkanoates via catalytic one-pot Mukaiyama-Aldol reactions.

Authors:  Lei Zhou; Michael P Doyle
Journal:  Org Lett       Date:  2010-02-19       Impact factor: 6.005

2.  Mitomycins syntheses: a recent update.

Authors:  Jean-Christophe Andrez
Journal:  Beilstein J Org Chem       Date:  2009-07-08       Impact factor: 2.883

Review 3.  Mukaiyama Aldol Reactions in Aqueous Media.

Authors:  Taku Kitanosono; Shū Kobayashi
Journal:  Adv Synth Catal       Date:  2013-10-31       Impact factor: 5.837

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.