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- W4308773968 endingPage "15985" @default.
- W4308773968 startingPage "15963" @default.
- W4308773968 abstract "A convenient and efficient synthetic strategy to prepare enantioenriched gem-difluoromethylenated spiro-pyrrolidinyl and spiro-piperidinyl oxindoles is described. Fluoride-mediated diastereoselective nucleophilic addition of PhSCF2SiMe3 to chiral N-tert-butanesulfinyl ketimines derived from isatins was a key step and provided diastereomeric adducts, which were readily separable. Removal of the chiral sulfinyl group followed by structural manipulation afforded chiral gem-difluoromethylenated spiro-pyrrolidinyl and spiro-piperidinyl oxindoles." @default.
- W4308773968 created "2022-11-15" @default.
- W4308773968 creator A5005844572 @default.
- W4308773968 creator A5018279372 @default.
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- W4308773968 creator A5044643514 @default.
- W4308773968 creator A5078131117 @default.
- W4308773968 creator A5078833398 @default.
- W4308773968 date "2022-11-11" @default.
- W4308773968 modified "2023-09-26" @default.
- W4308773968 title "Diastereoselective Addition of PhSCF<sub>2</sub>SiMe<sub>3</sub> to Chiral <i>N</i>-<i>tert</i>-Butanesulfinyl Ketimines Derived from Isatins: Synthesis of Enantioenriched <i>gem</i>-Difluoromethylenated Spiro-pyrrolidinyl and Spiro-piperidinyl Oxindoles" @default.
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- W4308773968 doi "https://doi.org/10.1021/acs.joc.2c02098" @default.