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Enantioselective benzoin condensation catalyzed by bifunctional N-heterocyclic carbenes
  • 时间:0
  • 分类:TQ463.4[化学工程—制药化工] O614.811[理学—无机化学;理学—化学]
  • 作者机构:[1]Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
  • 相关基金:This work was supported by the National Natural Science Foundation of China (20602036), the Ministry of Science and Technology of China (2009ZX09501-018) and the Chinese Academy of Sciences.
中文摘要:

安息香冷凝作用是重要碳碳形成契约的反应。有好产量,高 enantioselectivity 和宽广底层范围的安息香反应高度在器官的合成被需要。bifunctional 催化的分子间的安息香冷凝作用 N 杂环的 carbenes 被调查了,并且相应 -hydroxyketones 与收益被获得直到 76% 并且 enantioselectivities 直到 99% ee。

英文摘要:

Benzoin condensation is an important carbon-carbon bond-forming reaction. The benzoin reaction with good yield, high enantioselectivity and broad substrate scope is highly desired in organic synthesis. The intermolecular benzoin condensation catalyzed by bifunctional N-heterocyclic carbenes has been investigated, and the corresponding α-hydroxyketones were obtained with yields up to 76% and enantioselectivities up to 99% ee.

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