Reactions · Wikipedia: Category:Name reactions
Fukuyama coupling
Cross-coupling
Overview
The Fukuyama coupling is a coupling reaction taking place between a thioester and an organozinc halide in the presence of a palladium catalyst. The reaction product is a ketone. This reaction was discovered by Tohru Fukuyama et al. in 1998.
Actions
- This entry doesn't have stoichiometric equivalents on file yet — the Reaction Scale Calculator needs at least one participant tagged with an equivalents value.
- Mechanism / source ↗
- View as JSON ↗
Search literature
More Cross-coupling reactions
- 2-(4-METHOXYPHENYL)-2-CYCLOHEXEN-1-ONE: PREPARATION OF 2-IODO-2-CYCLOHEXEN-1-ONE AND SUZUKI COUPLING WITH 4-METHOXYPHENYLBORONIC ACID (2-Cyclohexen-1-one, 2-(4-methoxyphenyl)- and 2-Cyclohexen-1-one, 2-iodo-)) Cross-coupling
- ACCELERATED SUZUKI COUPLING VIA A LIGANDLESS PALLADIUM CATALYST: 4-METHOXY-2'-METHYLBIPHENYL (1,1'-Biphenyl, 4'-methoxy-2-methyl-) Cross-coupling
- ALKYNYL(PHENYL)IODONIUM TOSYLATES: PREPARATION AND STEREOSPECIFIC COUPLING WITH VINYLCOPPER REAGENTS. FORMATION OF CONJUGATED ENYNES. 1-HEXYNYL(PHENYL)IODONIUM TOSYLATE AND (E)-5-PHENYLDODEC-5-EN-7-YNE (Iodine, 1-hexynyl(4-methylbenzenesulfonato-O)phenyl- and Benzene, (1-butyl-1-octen-3-ynyl)-, (E)-) Cross-coupling
- B-PROTECTED HALOBORONIC ACIDS FOR ITERATIVE CROSS-COUPLING Cross-coupling
- Buchwald–Hartwig amination Cross-coupling
- Cadiot–Chodkiewicz coupling Cross-coupling