2010
DOI: 10.1080/00397910903009422
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Stereoselective Synthesis of Substituted 2-(Z-Styrylsulfonyl)-1H-imidazoles and Benzothiazole

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Cited by 10 publications
(4 citation statements)
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“…The syntheses of analogues of 3 were modified based on the procedures of Laufer et al 8 Briefly, 4,5-diphenyl-2-thioimidazole was treated with alkyl bromides to give thioethers 10. The thioether was either oxidized to the sulfone 11 first and alkylated 9 or, alternatively, alkylated and then oxidized to yield 13. 10 Deprotonating the benzylic α-carbon and fluorinating once or twice gave analogues 14a and 14b (Scheme 2).…”
mentioning
confidence: 99%
“…The syntheses of analogues of 3 were modified based on the procedures of Laufer et al 8 Briefly, 4,5-diphenyl-2-thioimidazole was treated with alkyl bromides to give thioethers 10. The thioether was either oxidized to the sulfone 11 first and alkylated 9 or, alternatively, alkylated and then oxidized to yield 13. 10 Deprotonating the benzylic α-carbon and fluorinating once or twice gave analogues 14a and 14b (Scheme 2).…”
mentioning
confidence: 99%
“…On the basis of the aforementioned observations and as a part of our research program in the synthesis of novel heterocyclic systems [17][18][19][20][21], we wish to report in this article the modified Hantzsch condensation of 2,4,6-tri-substituted pyridine derivatives catalyzed by CAN via multi-component approach in aqueous medium.…”
Section: Introductionmentioning
confidence: 99%
“…On the basis of the aforementioned observations and as a part of our research program in the synthesis of novel heterocyclic systems , we wish to report in this article the modified Hantzsch condensation of 2,4,6‐tri‐substituted pyridine derivatives catalyzed by CAN via multi‐component approach in aqueous medium.…”
Section: Introductionmentioning
confidence: 99%