Reactions of linear conjugated dienone structures with arenes under superelectrophilic activation conditions. An experimental and theoretical study of intermediate multicentered electrophilic species-Reference-Cited by-同舟云学术

Reactions of linear conjugated dienone structures with arenes under superelectrophilic activation conditions. An experimental and theoretical study of intermediate multicentered electrophilic species

Published:2022 Issue:25 Volume:46 Page:12041-12053
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Kochurin Matvei A.¹,Ismagilova Alina R.²,Zakusilo Dmitriy N.²,Khoroshilova Olesya V.¹^ORCID,Boyarskaya Irina A.¹,Vasilyev Aleksander V.¹²^ORCID

Affiliation:

1. Department of Organic Chemistry, Institute of Chemistry, Saint Petersburg State University, Universitetskaya nab., 7/9, Saint Petersburg, 199034, Russia

2. Department of Chemistry, Saint Petersburg State Forest Technical University, Institutsky per., 5, Saint Petersburg, 194021, Russia

Abstract

Reactions of conjugated dienones with arenes under superelectrophilic activation conditions result in the formation of conjugated enones, indanes, and carbocyclic structures.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ01828D

Reference39 articles.

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2. G. A.Olah and D. A.Klumpp , Superelectrophiles and Their Chemistry , Wiley , New York , 2008

3. Contemporary Carbocation Chemistry: Applications in Organic Synthesis

4. Trifluoromethanesulfonic acid in organic synthesis

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