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- W2079054039 endingPage "10955" @default.
- W2079054039 startingPage "10945" @default.
- W2079054039 abstract "Oxindoles substituted at N-1 by electron-withdrawing groups and at C-3 by ω-amino chains of various lengths undergo mild and easy isomerization to new 5- to 12-membered lactams in good yields (30–96%). As efficient asymmetric syntheses of diversely 3,3-disubstituted oxindoles are currently developed, this isomerization provides a new and valuable access to medium-sized lactams α-substituted with a quaternary asymmetric carbon bearing a 2-aminophenyl residue." @default.
- W2079054039 created "2016-06-24" @default.
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- W2079054039 date "2014-11-04" @default.
- W2079054039 modified "2023-10-07" @default.
- W2079054039 title "Synthesis of Lactams by Isomerization of Oxindoles Substituted at C-3 by an ω-Amino Chain" @default.
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- W2079054039 doi "https://doi.org/10.1021/jo501978j" @default.
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