Electrocyclic Reactions
Electrocyclic Reactions is a type of pericyclic reaction characterized by the intramolecular rearrangement of electrons in a conjugated π-system to form a new σ-bond between the termini of the system, resulting in the reduction of the number of π-bonds and the formation of a cyclic product with specific stereochemistry governed by orbital symmetry.
1K
Publications
39.7K
Citations
2.8K
Authors
641
Institutions
Publications per year
2017–2026
92
Parents
1K
1–5 of 1K
2.8K
26
h-index
21
h-index
19
h-index
12
h-index
12
h-index
1–5 of 2.8K
641

Centre National de la Recherche Scientifique
Paris, France
22 h-index
111 publications
4K citations
University of California, Los Angeles
Los Angeles, United States
20 h-index
83 publications
5.2K citations
Fukuyama University
Fukuyama, Japan
19 h-index
133 publications
4.7K citations

Kyoto University
Kyoto, Japan
13 h-index
46 publications
1.8K citations

Universidade de Vigo
Vigo, Spain
12 h-index
54 publications
1.8K citations
N.D. Zelinsky Institute of Organic Chemistry
Moscow, Russia
12 h-index
56 publications
1.9K citations

University of Alberta
Edmonton, Canada
12 h-index
34 publications
2.1K citations

Chinese Academy of Sciences
Beijing, China
11 h-index
35 publications
1.1K citations
1–8 of 641
JACS · 132 publications · 8.8K citations
50
h-index
JOC · 98 publications · 3.4K citations
35
h-index
OL · 60 publications · 2.5K citations
33
h-index
99 publications · 2.2K citations
27
h-index
38 publications · 2.4K citations
27
h-index
1–5