Hydride transfer mechanism in the catalytic allylation of norbornadiene with allyl formate
- 作者: Durakov S.A.1, Shamsiev R.S.1, Flid V.R.1, Gekhman A.E.2
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隶属关系:
- 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
- 期: 卷 67, 编号 12 (2018)
- 页面: 2234-2240
- 栏目: 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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详细
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.
作者简介
S. Durakov
MIREA – Russian Technological University, M. V. Lomonosov Institute of Fine Chemical Technologies
Email: vitaly-flid@yandex.ru
俄罗斯联邦, 86 prosp. Vernadskogo, Moscow, 119571
R. Shamsiev
MIREA – Russian Technological University, M. V. Lomonosov Institute of Fine Chemical Technologies
Email: vitaly-flid@yandex.ru
俄罗斯联邦, 86 prosp. Vernadskogo, Moscow, 119571
V. Flid
MIREA – Russian Technological University, M. V. Lomonosov Institute of Fine Chemical Technologies
编辑信件的主要联系方式.
Email: vitaly-flid@yandex.ru
俄罗斯联邦, 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
俄罗斯联邦, 31 Leninsky prosp., Moscow, 119991
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