Diastereoselective Synthesis of 3,4-Benzomorphan Derivatives via Tandem [5 + 1]/Hemiaminalization of (2-Aminoaryl)divinyl Ketones-Reference-Cited by-同舟云学术

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Diastereoselective Synthesis of 3,4-Benzomorphan Derivatives via Tandem [5 + 1]/Hemiaminalization of (2-Aminoaryl)divinyl Ketones

Published:2016-01-06 Issue:2 Volume:18 Page:324-327
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Yifei¹,Feng Chengjie¹,Shi Hui¹,Xu Xianxiu¹

Affiliation:

1. Department of Chemistry, Northeast Normal University, Changchun 130024, China

Funder

Ministry of Education of the People's Republic of China

National Natural Science Foundation of China

Young Scientific Research Foundation of Jilin Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b03506

Reference71 articles.

1. First Total Synthesis of (±)-Melinonine-E and (±)-Strychnoxanthine Using a Radical Cyclization Process as the Core Ring-Forming Step

2. Radical promoted cyclisations of trichloroacetamides with silyl enol ethers and enol acetates: the role of the hydride reagent [tris(trimethylsilyl)silane vs. tributylstannane]

3. Regioselective Synthesis of Bridged Azabicyclic Compounds Using Radical Translocation/Cyclization Reactions of 4-Alkynyl-1-(o-iodobenzoyl)piperidines

4. Total Synthesis of the Immunosuppressant FR901483 via an Amidoacrolein Cycloaddition

5. Tandem Cationic aza-Cope Rearrangement−Mannich Cyclization Approach to the Core Structure of FR901483 via a Bridgehead Iminium Ion

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