BF3·OEt2-Promoted Propargyl Alcohol Rearrangement/[1,5]-Hydride Transfer/Cyclization Cascade Affording Tetrahydroquinolines-Reference-Cited by-同舟云学术

BF3·OEt2-Promoted Propargyl Alcohol Rearrangement/[1,5]-Hydride Transfer/Cyclization Cascade Affording Tetrahydroquinolines

Published:2019-05-22 Issue:11 Volume:21 Page:3990-3993
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhao Shuang¹,Wang Xiaoyang¹,Wang Pengfei¹,Wang Guangwei¹^ORCID,Zhao Wentao¹,Tang Xiangyang¹,Guo Minjie²

Affiliation:

1. Tianjin Key Laboratory of Molecular Optoelectronic Science, Department of Chemistry, School of Science, Tianjin University, Tianjin 300072, P. R. China

2. Institute for Molecular Design and Synthesis, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, P. R. China

Funder

Natural Science Foundation of Tianjin City

Ministry of Science and Technology of the People's Republic of China

Tianjin University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b01153

Reference55 articles.

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2. First Total Synthesis of Martinellic Acid, a Naturally Occurring Bradykinin Receptor Antagonist

3. Cycloaddition Reactions of Imines with 3-Thiosuccinic Anhydrides: Synthesis of the Tricyclic Core of Martinellic Acid

4. CH Bond Functionalization through Intramolecular Hydride Transfer

5. Advancement in Cascade [1,n]-Hydrogen Transfer/Cyclization: A Method for Direct Functionalization of Inactive C(sp3)H Bonds

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