4.4 Article

Asymmetric benzoin condensation promoted by chiral triazolium precatalyst bearing a pyridine moiety

期刊

TETRAHEDRON
卷 68, 期 3, 页码 894-899

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2011.11.028

关键词

N-Heterocyclic carbene; Catalytic asymmetric reaction; Benzoin condensation

资金

  1. Japan Science and Technology Agency [221Z03585]
  2. Kanazawa University
  3. Grants-in-Aid for Scientific Research [21550038, 24750037] Funding Source: KAKEN

向作者/读者索取更多资源

Chiral triazolium salts bearing a pyridine ring were developed as N-heterocyclic carbene precursors. In the presence of the chiral triazolium salt and a base, the catalytic asymmetric benzoin condensation proceeded to afford the product in high level of chemical yield and enantioselectivity. A wide range of aromatic aldehydes were applicable to this reaction. (C) 2011 Elsevier Ltd. All rights reserved.

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