4.7 Article

Enantio- and Diastereoselective Synthesis of Spiro-epoxyoxindoles

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 79, 期 9, 页码 3924-3929

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jo5003856

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资金

  1. National Natural Science Foundation of China [21232003, 21202053, 21272087]
  2. National Basic Research Program of China [2011CB808603]
  3. China Scholarship Concil

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An asymmetric synthesis of epoxyoxindoles from isatins has been developed by employing chiral sulfur ylides generated in situ from camphor-derived sulfonium salts. This reaction allows an efficient access to enantioenriched spiro-epoxyoxindoles under mild reaction conditions, featuring high yields and excellent enantio- and diastereoselectivities.

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