2005
DOI: 10.1016/j.tetlet.2005.04.112
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Regioselective Michael-induced cyclisation of γ- and δ-hydroxy vinyl sulfides and vinyl dithiocarbamates

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Cited by 25 publications
(23 citation statements)
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“…Vinyl sulfides play an important role in the synthesis of pharmaceutical and natural products [87][88][89]. An impressive one-pot conversion of alkenes into the corresponding enol sulfides was carried out via the N-bromosuccinimide cobromination reaction of alkenes with various thiols in basic medium [90].…”
Section: Synthesis Of Sulfides Via the Addition Of Thiols To Unsaturamentioning
confidence: 99%
“…Vinyl sulfides play an important role in the synthesis of pharmaceutical and natural products [87][88][89]. An impressive one-pot conversion of alkenes into the corresponding enol sulfides was carried out via the N-bromosuccinimide cobromination reaction of alkenes with various thiols in basic medium [90].…”
Section: Synthesis Of Sulfides Via the Addition Of Thiols To Unsaturamentioning
confidence: 99%
“…21 As a useful synthon, organic dithiocarbamates have been extensively used for the synthesis of structurally diverse biological potent scaffolds such as isothiocyanates, 22 thiourea, 23 cynamide, 24 dithiobenzophene, 25 glycosides, 26 amide, 27 dicarboxylates, 28 benzimidazole, 29 carbamate, 30 pyran, 31 flavonoids 32 etc. In view of their tremendous importance and wide applications, their syntheses have gained considerable attention, and therefore have become a focus of synthetic organic chemistry.…”
Section: Etcmentioning
confidence: 99%
“…Workup of the reaction resulted in a yellow oil (0.3062 g, 87%). 1 Phenyl(4-((3-(styrylthio)propyl)thio)phenyl)methanone (8). The title compound was prepared using the general procedure with 4-bromobenzophenone (0.2609 g, 1.0 mmol).…”
Section: Scheme 4 Control Experimentsmentioning
confidence: 99%
“…Workup of the reaction resulted in an orange oil (0.2294 g, 80%). 1 The Journal of Organic Chemistry Article…”
Section: Scheme 4 Control Experimentsmentioning
confidence: 99%