Electrochemical Ring-Opening of Cyclopropylamides with Alcohols toward the Synthesis of 1,3-Oxazines-Reference-Cited by-同舟云学术

Electrochemical Ring-Opening of Cyclopropylamides with Alcohols toward the Synthesis of 1,3-Oxazines

Published:2023-12-21 Issue: Volume: Page:
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Xu Peng-Cheng¹,Qian Shencheng¹,Meng Xiangtai²,Zheng Yu¹^ORCID,Huang Shenlin¹^ORCID

Affiliation:

1. Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources International Innovation Center for Forest Chemicals and Materials, Nanjing Forestry University, Nanjing, Jiangsu 210037, China

2. Sinopec Maoming Petrochemical Company, Maoming, Guangdong 525000, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c03537

Reference43 articles.

1. Formal Cycloadditions Driven by the Homolytic Opening of Strained, Saturated Ring Systems

2. Selective Carbon–Carbon Bond Cleavage of Cyclopropylamine Derivatives

3. Activation of aminocyclopropanes via radical intermediates

4. Catalytic (3 + 2) annulation of donor–acceptor aminocyclopropane monoesters and indoles

5. An endo ‐Directing‐Group Strategy Unlocks Enantioselective (3+1+2) Carbonylative Cycloadditions of Aminocyclopropanes

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