Wittig Reaction
The Wittig Reaction is an organic chemical reaction in which an aldehyde or ketone undergoes nucleophilic addition with a phosphonium ylide to form an alkene, distinguished by the formation of a carbon–carbon double bond through the transformation of a carbonyl group into a vinyl group.
2.7K
Publications
98.7K
Citations
7.4K
Authors
1.2K
Institutions
Publications per year
2017–2026
204
Variants
Wittig Olefination
Parents
2.7K
Synthesis of a carbon nanobelt
Guillaume Povie, Yasutomo Segawa, Taishi Nishihara et al. · Science · 2017 · 584 citations · Full text
1–5 of 2.7K
7.4K
20
h-index
19
h-index
18
h-index
17
h-index
17
h-index
1–5 of 7.4K
1.2K

Centre National de la Recherche Scientifique
Paris, France
29 h-index
221 publications
7.2K citations

Chinese Academy of Sciences
Beijing, China
25 h-index
183 publications
10.1K citations
Tokyo Institute of Technology
Tokyo, Japan
22 h-index
134 publications
3.6K citations
Shanghai Institute of Organic Chemistry
Shanghai, China
22 h-index
107 publications
6.3K citations
Central China Normal University
Wuhan, China
20 h-index
141 publications
4K citations
Laboratoire de Chimie Organique
Paris, France
19 h-index
110 publications
3.3K citations
National Taiwan Normal University
Taipei, Taiwan
18 h-index
111 publications
4.1K citations
The University of Tokyo
Tokyo, Japan
17 h-index
97 publications
5.1K citations
1–8 of 1.2K
JACS · 111 publications · 9K citations
60
h-index
JOC · 298 publications · 12.2K citations
58
h-index
OL · 126 publications · 5.7K citations
48
h-index
260 publications · 7.3K citations
40
h-index
121 publications · 4.6K citations
35
h-index
1–5