Carbocation Intermediates
Carbocation Intermediates is a reaction intermediate characterized by a trivalent, electron-deficient carbon atom bearing a positive formal charge, formed during the course of organic reactions where bond heterolysis generates an electron-poor center susceptible to nucleophilic attack.
543
Publications
23.7K
Citations
1.8K
Authors
495
Institutions
Publications per year
2017–2026
140
Variants
Carbocations
Parents
543
Hindered dialkyl ether synthesis with electrogenerated carbocations
Jinbao Xiang, Ming Shang, Yu Kawamata et al. · Nature · 2019 · 394 citations
Douglas A. Whittington, Mitchell L. Wise, Marek Urbanský et al. · Proceedings of the National Academy of Sciences · 2002 · 321 citations · Full text
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495
University of California, Davis
Davis, United States
21 h-index
58 publications
2.9K citations

Chinese Academy of Sciences
Beijing, China
14 h-index
51 publications
1.9K citations
University of Pennsylvania
Philadelphia, United States
11 h-index
40 publications
3.7K citations

Kyoto University
Kyoto, Japan
10 h-index
24 publications
618 citations
University of Illinois Urbana-Champaign
Urbana, United States
9 h-index
38 publications
4.5K citations
Case Western Reserve University
Cleveland, United States
9 h-index
21 publications
353 citations
The University of Tokyo
Tokyo, Japan
8 h-index
39 publications
1.5K citations
University at Buffalo, State University of New York
Buffalo, United States
8 h-index
17 publications
445 citations
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JACS · 95 publications · 5.3K citations
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JOC · 74 publications · 2.1K citations
25
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OL · 36 publications · 1.2K citations
23
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29 publications · 2.1K citations
22
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14 publications · 679 citations
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