Synthesis of 2,2,5-Trisubstituted 2H-Pyrroles and 2,3,5-Trisubstituted 1H-Pyrroles by Ligand-Controlled Site-Selective Dearomative C2-Arylation and Direct C3-Arylation-Reference-Cited by-同舟云学术

Synthesis of 2,2,5-Trisubstituted 2H-Pyrroles and 2,3,5-Trisubstituted 1H-Pyrroles by Ligand-Controlled Site-Selective Dearomative C2-Arylation and Direct C3-Arylation

Published:2019-08-09 Issue:17 Volume:21 Page:6972-6977
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yamaguchi Miyuki¹,Fujiwara Sakiko¹,Manabe Kei¹^ORCID

Affiliation:

1. School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Hamamatsu Foundation for Science and Technology Promotion

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02559

Reference62 articles.

1. Pyrrole: An emerging scaffold for construction of valuable therapeutic agents

2. Living on pyrrolic foundations – Advances in natural and artificial bioactive pyrrole derivatives

3. Pyrrole: a resourceful small molecule in key medicinal hetero-aromatics

4. Dimeric pyrrole–imidazole alkaloids: synthetic approaches and biosynthetic hypotheses

5. Synthesis of natural products containing the pyrrolic ring

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