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- W3136366692 abstract "The first representatives of (O-Si) chelated N-[(trifluorosilyl)methyl]anilides were synthesized. N-(Trimethylsilyl)acetanilide reacts with bifunctional silane ClCH2SiF3 with the formation of N-[(trifluorosilyl)methyl]acetanilide as the only product. N-[(Trifluorosilyl)methyl]benzanilide was obtained by similar alkylation of benzanilide with ClCH2SiF3 in the presence of DBU as a base. The structure of the products was proved by NMR and X-ray analysis. The energy of the C=O→Si dative bond in the obtained anilides was estimated by the QTAIM analysis. The calculated values lie near 40 kcal/mol, which is larger than in previously studied N-[difluoro(methyl)silyl]methylcarboxamides (14–30 kcal/mol)." @default.
- W3136366692 created "2021-03-29" @default.
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- W3136366692 date "2021-05-01" @default.
- W3136366692 modified "2023-09-26" @default.
- W3136366692 title "N-[(Trifluorosilyl)methyl]carboxanilides: Synthesis and structural features" @default.
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- W3136366692 doi "https://doi.org/10.1016/j.jorganchem.2021.121788" @default.
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