Hydride transfer mechanism in the catalytic allylation of norbornadiene with allyl formate
- Авторы: Durakov S.A.1, Shamsiev R.S.1, Flid V.R.1, Gekhman A.E.2
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Учреждения:
- MIREA – Russian Technological University, M. V. Lomonosov Institute of Fine Chemical Technologies
- N. S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
- Выпуск: Том 67, № 12 (2018)
- Страницы: 2234-2240
- Раздел: Full Articles
- URL: https://ogarev-online.ru/1066-5285/article/view/243222
- DOI: https://doi.org/10.1007/s11172-018-2361-7
- ID: 243222
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Аннотация
Allylation of norbornadiene with allyl formate in the presence of the palladium catalytic systems is characterized by several peculiarities associated with the new reaction route: hydroallylation (reductive allylation) occurs along with the traditional allylation (oxidative allylation). Both processes are considered from the single point of view, and the mechanism assuming different routes of the hydride transfer in the key intermediates was proposed. It was proved by using deuterated reactants that the hydride transfer can involve the allyl, norbornenyl, or formyl moieties. In all cases, the hydrogen atom bound to the carbon atom in the β-position relative to palladium is eliminated in this step.
Об авторах
S. Durakov
MIREA – Russian Technological University, M. V. Lomonosov Institute of Fine Chemical Technologies
Email: vitaly-flid@yandex.ru
Россия, 86 prosp. Vernadskogo, Moscow, 119571
R. Shamsiev
MIREA – Russian Technological University, M. V. Lomonosov Institute of Fine Chemical Technologies
Email: vitaly-flid@yandex.ru
Россия, 86 prosp. Vernadskogo, Moscow, 119571
V. Flid
MIREA – Russian Technological University, M. V. Lomonosov Institute of Fine Chemical Technologies
Автор, ответственный за переписку.
Email: vitaly-flid@yandex.ru
Россия, 86 prosp. Vernadskogo, Moscow, 119571
A. Gekhman
N. S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
Email: vitaly-flid@yandex.ru
Россия, 31 Leninsky prosp., Moscow, 119991
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