2009
DOI: 10.3998/ark.5550190.0010.105
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One-pot synthesis of sulfur heterocycles from simple organic substrates

Abstract: Sulfur-nitrogen heterocycles are important compounds due to their unusual physical properties and significant and versatile biological activity. A novel strategy for their preparation from readily available organic substrates with the employment of sulfur monochloride is proposed. A synthesis of wide range of heterocyclic systems including 1,2-dithioles, 1,2,3,4,5-pentathiepins, 1,2,3-dithiazoles, 1,4-thiazines, 1,2,3,4,5,6,7-heptathiocanes and others, in a cascade transformations has been developed.

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Cited by 16 publications
(2 citation statements)
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“…α,β-Unsaturated ketones like Chalcons undergo a variety of useful reactions to produce a large number of their derivatives specialy heterocyclic derivatives [1][2][3][4][5]. A large number of Schiff bases were prepared and their biological activity were investigated and found to be very good antibacterial, antifungal agents [6][7][8].…”
Section: Introductionmentioning
confidence: 99%
“…α,β-Unsaturated ketones like Chalcons undergo a variety of useful reactions to produce a large number of their derivatives specialy heterocyclic derivatives [1][2][3][4][5]. A large number of Schiff bases were prepared and their biological activity were investigated and found to be very good antibacterial, antifungal agents [6][7][8].…”
Section: Introductionmentioning
confidence: 99%
“…A specific feature of sulfur monochloride (S 2 Cl 2 ) is its diverse reactivity [15,16,17,18]. The most useful property of this compound is its sulfurating ability.…”
Section: Introductionmentioning
confidence: 99%