Microwave- and Thermally Promoted Iminyl Radical Cyclizations: A Versatile Method for the Synthesis of Functionalized Pyrrolines-Reference-Cited by-同舟云学术

Microwave- and Thermally Promoted Iminyl Radical Cyclizations: A Versatile Method for the Synthesis of Functionalized Pyrrolines

Published:2022-12-06 Issue:24 Volume:87 Page:16250-16262
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Singh Jatinder¹,Nelson Tanner J.¹,Mansfield Samuel A.¹^ORCID,Nickel Garrison A.¹,Cai Yu¹^ORCID,Jones Dakota D.¹,Small Jeshurun E.¹,Ess Daniel H.¹^ORCID,Castle Steven L.¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, United States

Funder

Division of Chemistry

Brigham Young University

American Chemical Society Petroleum Research Fund

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c01806

Reference73 articles.

1. Synthetic Strategies for 5- and 6-Membered Ring Azaheterocycles Facilitated by Iminyl Radicals

2. Recent Advances in Iminyl Radical Cyclizations

3. Synthesis of Nitrogen-Containing Heterocycles via Imidoyl or Iminyl Radical Intermediates

4. Recent advances in iminyl radical-mediated catalytic cyclizations and ring-opening reactions

5. Recent advances in cyclization reactions of unsaturated oxime esters (ethers): synthesis of versatile functionalized nitrogen-containing scaffolds

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