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- W2022160579 abstract "Les structures d'imines et d'oxazirannes dérivés de la méthyl-2 et de la diméthyl-2,6 cyclohexanone ont été déterminées par RMN 1H. Nous avons pu montrer que pour tous les oxazirannes étudiés, la conformation préférentielle correspond à une position équatoriale de l'azote. The structures of imines and oxaziridines derived from 2-methyl and 2,6-dimethyl cyclohexanone have been determined by 1H n.m.r. spectroscopy. The preferred conformation of all the oxaziridines we examined was found to have the nitrogen atom in equatorial position." @default.
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- W2022160579 date "1976-12-01" @default.
- W2022160579 modified "2023-10-16" @default.
- W2022160579 title "Photolyse d'oxazirannes: VI—Détermination par RMN du proton des configurations et conformations privilégiées d'oxazirannes à jonction spirannique" @default.
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- W2022160579 doi "https://doi.org/10.1002/mrc.1270081203" @default.
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