4.8 Article

PyBidine-Ni(OAc)2-Catalyzed Michael/AIdoI Reaction of Methyleneindolinones and Thiosalicylaldehydes for Stereochemically Divergent Thiochromanyl-spirooxindoles

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ORGANIC LETTERS
卷 18, 期 22, 页码 5824-5827

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b02783

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资金

  1. JSPS KAKENHI [JP16H01004]
  2. Workshop on Chirality at Chiba University (WCCU)
  3. Grants-in-Aid for Scientific Research [16H01004] Funding Source: KAKEN

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(S,S)-Diphenylethylenediamine-derived bis(imidazolidine)pyridine (PyBidine)-Ni(OAc)(2) complex catalyzed the asymmetric Michael/aldol reaction of methyleneindolinone and thiosalicylaldehyde to produce (2'R,3S,4'R)-thiochromanyl-spirooxindole having three contiguous stereogenic centers.

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