Literature DB >> 15524429

Highly enantioselective phenylacetylene additions to ketones catalyzed by (S)-BINOL-Ti complex.

Yifeng Zhou1, Rui Wang, Zhaoqing Xu, Wenjin Yan, Lei Liu, Yongfeng Kang, Zhijian Han.   

Abstract

The readily available and inexpensive (S)-BINOL ligand in combination with Ti(O(i)Pr)(4) is an effective chiral catalyst for the catalytic asymmetric addition of alkynylzinc to unactivated simple ketones. Good to excellent enantioselectivities were achieved. No previous case has been reported successfully using BINOL to catalyze the addition of phenylacetylene to unactivated ketones, and thus the utility of BINOL in asymmetric catalysis is expanded.

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Year:  2004        PMID: 15524429     DOI: 10.1021/ol0485621

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


  2 in total

1.  The Enantioselective Addition of Alkyne Nucleophiles to Carbonyl Groups.

Authors:  Barry M Trost; Andrew H Weiss
Journal:  Adv Synth Catal       Date:  2009-05       Impact factor: 5.837

2.  Asymmetric synthesis of tertiary benzylic alcohols.

Authors:  Monika I Antczak; Feng Cai; Joseph M Ready
Journal:  Org Lett       Date:  2010-12-13       Impact factor: 6.005

  2 in total

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