Synthesis of new chiral amidophosphite ligands and their application in hydrogenation of benzodiazepinones and enamides
- Авторы: Sokolovskaya M.V.1, Lyubimov S.E.1, Davankov V.A.1
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Учреждения:
- A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
- Выпуск: Том 66, № 7 (2017)
- Страницы: 1213-1216
- Раздел: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/240926
- DOI: https://doi.org/10.1007/s11172-017-1875-8
- ID: 240926
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Аннотация
New chiral amidophosphites were synthesized and tested in the Ir-catalyzed hydrogenation of 4-substituted 1,3-dihydro-2H-1,5-benzodiazepin-2-ones and Rh-catalyzed hydrogenation of dehydro amino acid derivatives. The triphenylphosphine additive can considerably increase the enantioselectivity of both processes.
Об авторах
M. Sokolovskaya
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: lssp452@mail.ru
Россия, 28 ul. Vavilova, Moscow, 119991
S. Lyubimov
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Автор, ответственный за переписку.
Email: lssp452@mail.ru
Россия, 28 ul. Vavilova, Moscow, 119991
V. Davankov
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: lssp452@mail.ru
Россия, 28 ul. Vavilova, Moscow, 119991
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