4.4 Article

Ag/ThioClickFerrophos catalyzed highly enantioselective 1,3-dipolar cycloaddition of azomethine ylides with alkenes

期刊

TETRAHEDRON LETTERS
卷 51, 期 38, 页码 5068-5070

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2010.07.085

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资金

  1. Japan Society for the Promotion of Science (JSPS) [22550044]
  2. Chuo University
  3. Grants-in-Aid for Scientific Research [22550044] Funding Source: KAKEN

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A silver(I)/ThioClickFerrophos complex catalyzed the endo selective asymmetric 1,3-dipolar cycloaddition reaction of methyl N-benzylideneglycinate (the source of azomethine ylides) with alpha,beta-unsaturated esters and maleimides to give the endo-2,4,5- and 2,3,4,5-substituted pyrrolidines in good yields with high enantioselectivities (up to 99% ee). The complex also effectively catalyzed the endo selective reactions with beta-nitrostyrene to give the 4-nitropyrrolidine in a high enantioselectivity. (C) 2010 Elsevier Ltd. All rights reserved.

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