Povarov Reaction of Cycloiminium Formed in Situ via Hydroamination Cycloisomerization of Homopropargylic Amines with Electron-Rich Olefins-Reference-Cited by-同舟云学术

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Povarov Reaction of Cycloiminium Formed in Situ via Hydroamination Cycloisomerization of Homopropargylic Amines with Electron-Rich Olefins

Published:2017-01-06 Issue:2 Volume:82 Page:950-958
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liu Qiangqiang¹,Wang Chan¹,Li Qiang¹,Hou Yajie¹,Wu Ye¹,Liu Lingyan¹^ORCID,Chang Weixing¹,Li Jing¹²

Affiliation:

1. State Key Laboratory and Institute of Elemento-Organic Chemistry, the College of Chemistry, Nankai University, Tianjin 300071, China

2. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Weijin Road 94, Nankai District, Tianjin 300071, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02496

Reference42 articles.

1. αβ-UNSATURATED ETHERS AND THEIR ANALOGUES IN REACTIONS OF DIENE SYNTHESIS

2. Recent synthetic developments in a powerful imino Diels–Alder reaction (Povarov reaction): application to the synthesis of N-polyheterocycles and related alkaloids

3. Synthesis of substituted 1,2,3,4-tetrahydroquinones by the Povarov reaction. New potentials of the classical reaction

4. Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels–Alder Reaction

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4. The povarov reaction in the synthesis of <i>N</i>-polycyclic compounds with a tetrahydroquinoline fragment;Журнал органической химии;2023-07-15

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