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• W4225289115 abstract "An efficient tosylhydrazine-mediated conjugate reduction of 3-phenacylideneoxindole and sequential Michael/intramolecular aldol reaction is reported under base-catalyzed conditions towards the formation of densely substituted dispirocyclopentanebisoxindole derivatives. The reaction proceeded in a diastereoselective manner to afford four chiral stereocenters. The method also has advantages of wide substrate scope, readily available starting materials and operational simplicity through one pot reaction." @default.
• W4225289115 created "2022-05-05" @default.
• W4225289115 creator A5008173964 @default.
• W4225289115 creator A5013544376 @default.
• W4225289115 date "2022-04-27" @default.
• W4225289115 modified "2023-09-25" @default.
• W4225289115 title "Tosylhydrazine-promoted self-conjugate reduction–Michael/aldol reaction of 3-phenacylideneoxindoles towards dispirocyclopentanebisoxindole derivatives" @default.
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• W4225289115 doi "https://doi.org/10.3762/bjoc.18.49" @default.
• W4225289115 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35558650" @default.
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