Photorearrangement of dihetarylethenes as a tool for the benzannulation of heterocycles-Reference-Cited by-同舟云学术

Photorearrangement of dihetarylethenes as a tool for the benzannulation of heterocycles

Published:2019 Issue:20 Volume:17 Page:4990-5000
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Lvov Andrey G.¹²³⁴^ORCID,Kavun Alexey M.¹²³⁴⁵,Kachala Vadim V.¹²³⁴,Lyssenko Konstantin A.⁶⁷⁸⁴,Shirinian Valerii Z.¹²³⁴^ORCID

Affiliation:

1. N. D. Zelinsky Institute of Organic Chemistry

2. Russian Academy of Sciences

3. Moscow

4. Russian Federation

5. Higher Chemical College

6. Department of Chemistry

7. Lomonosov Moscow State University

8. 119992 Moscow

Abstract

The photochemical rearrangement of dihetarylethenes is a powerful tool for the benzannulation of heterocycles, providing a wide scope of benzannulated heterocycles and N-, S-, C-, and O-substituents in the newly formed benzene ring.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB00690G

Reference87 articles.

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2. Indole synthesis – something old, something new

3. Recent trends in the synthesis of carbazoles: an update

4. Benzannulation

5. Recent developments in synthetic methods for benzo[b]heteroles

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