Literature DB >> 16010332

Acyclic amino acid-catalyzed direct asymmetric aldol reactions: alanine, the simplest stereoselective organocatalyst.

Armando Córdova1, Weibiao Zou, Ismail Ibrahem, Efraim Reyes, Magnus Engqvist, Wei-Wei Liao.   

Abstract

The linear amino acid-catalyzed direct asymmetric intermolecular aldol reaction is presented; simple amino acids such as alanine, valine, isoleucine, aspartate, alanine tetrazole and serine catalyzed the direct catalytic asymmetric intermolecular aldol reactions between unmodified ketones and aldehydes with excellent stereocontrol and furnished the corresponding aldol products in up to 98% yield and with up to > 99% ee.

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Year:  2005        PMID: 16010332     DOI: 10.1039/b507968n

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Asymmetric catalytic N-phosphonyl imine chemistry: the use of primary free amino acids and Et2AlCN for asymmetric catalytic Strecker reaction.

Authors:  Parminder Kaur; Suresh Pindi; Walter Wever; Trideep Rajale; Guigen Li
Journal:  J Org Chem       Date:  2010-08-06       Impact factor: 4.354

2.  Asymmetric aldol reactions of α,β-unsaturated ketoester substrates catalyzed by chiral diamines.

Authors:  Sha-Sha Kan; Jian-Zhen Li; Cheng-Yan Ni; Quan-Zhong Liu; Tai-Ran Kan
Journal:  Molecules       Date:  2011-05-04       Impact factor: 4.411

3.  Prebiotically Plausible Organocatalysts Enabling a Selective Photoredox α-Alkylation of Aldehydes on the Early Earth.

Authors:  Anna C Closs; Elina Fuks; Maximilian Bechtel; Oliver Trapp
Journal:  Chemistry       Date:  2020-08-12       Impact factor: 5.236

  3 in total

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