1990
DOI: 10.1002/chin.199003190
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ChemInform Abstract: Heterocyclic Enamides Studies. Part 1. Preparation of 4‐Bromo‐ and 4‐Chloroisoquinolines from 1,2‐Dihydroisoquinoline Derivatives.

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“…419 1,2-Dihydroisoquino-line derivatives, on treatment with bromine, undergo bromination at the unsaturated C-4 carbon. 420 Reaction of bromine with 4,6-dimethyl-2-(allylthio)pyrimidine produced the corresponding 3-(bromomethyl)-5,7-dimethyl-2,3-dihydrothiazolo[3,2-a]pyrimidinium bromogenides. 421 422 Kim et al brominated 1-vinyl-2-pyridone with bromine in methanol to produce the corresponding bicyclic adduct in 25% yield.…”
Section: Bromination Reactions 31 Bromination With Molecular Brominementioning
confidence: 99%
See 1 more Smart Citation
“…419 1,2-Dihydroisoquino-line derivatives, on treatment with bromine, undergo bromination at the unsaturated C-4 carbon. 420 Reaction of bromine with 4,6-dimethyl-2-(allylthio)pyrimidine produced the corresponding 3-(bromomethyl)-5,7-dimethyl-2,3-dihydrothiazolo[3,2-a]pyrimidinium bromogenides. 421 422 Kim et al brominated 1-vinyl-2-pyridone with bromine in methanol to produce the corresponding bicyclic adduct in 25% yield.…”
Section: Bromination Reactions 31 Bromination With Molecular Brominementioning
confidence: 99%
“…The reaction of [(methoxycarbonyl)methylene]tetrahydroquinoxalinone with aqueous bromine resulted in the formation of the corresponding monobromo product . 1,2-Dihydroisoquinoline derivatives, on treatment with bromine, undergo bromination at the unsaturated C-4 carbon . Reaction of bromine with 4,6-dimethyl-2-(allylthio)pyrimidine produced the corresponding 3-(bromomethyl)-5,7-dimethyl-2,3-dihydrothiazolo[3,2- a ]pyrimidinium bromogenides .…”
Section: Bromination Reactionsmentioning
confidence: 99%