1997
DOI: 10.1055/s-1997-1291
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A Convenient Oxidative Dethioacetalization of 1,3-Dithiolanes and 1,3-Dithianes with Iron(III) Nitrate and Montmorillonite K10 in Hexane

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Cited by 32 publications
(10 citation statements)
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“…For (n ϭ 2,3): N-Chlorobenzotriazole, CH 2 Cl 2 , Ϫ80ЊC; NaOH, 50% yield. When the reaction was run in MeOH, a dimethyl ketal was produced that could be hydrolyzed with AcOH 3 and Montmorillonite K10 clay in hexane 148 and Fe(NO 3 ) 3 /basic alumina are also effective. 20.…”
Section: Methods That Form An Acid In Situmentioning
confidence: 99%
“…For (n ϭ 2,3): N-Chlorobenzotriazole, CH 2 Cl 2 , Ϫ80ЊC; NaOH, 50% yield. When the reaction was run in MeOH, a dimethyl ketal was produced that could be hydrolyzed with AcOH 3 and Montmorillonite K10 clay in hexane 148 and Fe(NO 3 ) 3 /basic alumina are also effective. 20.…”
Section: Methods That Form An Acid In Situmentioning
confidence: 99%
“…The Mannich bases exhibit anticonvulsant [9,10], antitubercular [11], antimalarial [12], anti-HIV [13], anti-viral [14], and anti-cancer [15] activities.…”
Section: Original Research Articlementioning
confidence: 99%
“…SOCl 2 -treated silica and DMSO is a good combination with which to cleave 2-substituted-1,3-dithiolanes; however, under similar conditions 2,2-disubstituted-1,3-dithiolanes undergo ring expansion to give dihydro-1,4-dithiins [212]. Recent methods for the cleavage of 1,3-dithiolanes include the use of 2,4,6-trichlorotriazine and DMSO [213], oxone on wet alumina [214] and ferric nitrate on K-10 montmorillonite clay [215].…”
Section: Cleavage Reactionsmentioning
confidence: 99%