19 research outputs found
Dithiophosphorylation of paracetamol
Get PDF漏 2014 Pleiades Publishing, Ltd. Paracetamol smoothly reacted with 2,4-diaryl-1,3,2位5,4位5-dithiadiphosphetane 2,4-disulfides to give O-[4-(acetylamino)phenyl] hydrogen arylphosphonodithioates
Dithiophosphorylation of nerol and geraniol trimethylsilyl derivatives
Get PDF漏 2017, Pleiades Publishing, Ltd.Reaction of tetraphosphorus decasulfide with 袨-(cis- and trans-3,7-dimethylocta-2,6-dien-1-yl)-trimethylsilanes affords 袨,袨-bis(cis- and trans-3,7-dimethylocta-2,6-dien-1-yl) S-(trimethylsilyl)dithiophosphates
Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol
Get PDF漏 2016, Pleiades Publishing, Ltd.Carvacrol trimethylsilyl ether when reacting with P4S10 forms S-trimethylsilyl ester of O,O-bis(5-isopropyl-2-methylphenyl)dithiophosphoric acid. The reactions of 2,4-diorganyl-1,3,2,4-dithiadiphosphetane-2,4-disulfides with carvacrol (thymol) trimethylsilyl ether yield the S-trimethylsilyl esters of the corresponding dithiophosphoric acids
2,4-Diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides, their structure and S-silyl dithiophosphonic derivatives
Get PDF漏 2016 Taylor & Francis Group, LLC.Novel 2,4-diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfideswere prepared by the reactions of tetraphosphorus decasulfide with butylphenyl ether or 3-brominephenyl-1-isoamyl ether in 1,2-dichlorobenzene. Their structures were established by X-ray single crystal diffraction. Chiral S-trimethylsilyl dithiophosphonates were prepared by the reactions of 2,4-diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides with trimethyl silyl ethers of monoterpenols. Unsaturated S-trimethylsilyl dithiophosphonates were synthesized by the reactions of 2,4-diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides with O-trimethylsilyl ethers of geraniol, nerol, and (R,S)-linalool. S-Esters of dithiophosphonic acids, which possessed antimicrobial activity, were prepared by the reactions of chiral S-trimethylsilyl dithiophosphonateswith orthoformiates, acetals and thioacetals
Dithiophosphorylation of paracetamol
No full text漏 2014 Pleiades Publishing, Ltd. Paracetamol smoothly reacted with 2,4-diaryl-1,3,2位5,4位5-dithiadiphosphetane 2,4-disulfides to give O-[4-(acetylamino)phenyl] hydrogen arylphosphonodithioates
Dithiophosphorylation of paracetamol
Get PDF漏 2014 Pleiades Publishing, Ltd. Paracetamol smoothly reacted with 2,4-diaryl-1,3,2位5,4位5-dithiadiphosphetane 2,4-disulfides to give O-[4-(acetylamino)phenyl] hydrogen arylphosphonodithioates
Dithiophosphorylation of paracetamol
No full text漏 2014 Pleiades Publishing, Ltd. Paracetamol smoothly reacted with 2,4-diaryl-1,3,2位5,4位5-dithiadiphosphetane 2,4-disulfides to give O-[4-(acetylamino)phenyl] hydrogen arylphosphonodithioates
Dithiophosphorylation of nerol and geraniol trimethylsilyl derivatives
No full text漏 2017, Pleiades Publishing, Ltd.Reaction of tetraphosphorus decasulfide with 袨-(cis- and trans-3,7-dimethylocta-2,6-dien-1-yl)-trimethylsilanes affords 袨,袨-bis(cis- and trans-3,7-dimethylocta-2,6-dien-1-yl) S-(trimethylsilyl)dithiophosphates
Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol
Get PDF漏 2016, Pleiades Publishing, Ltd.Carvacrol trimethylsilyl ether when reacting with P4S10 forms S-trimethylsilyl ester of O,O-bis(5-isopropyl-2-methylphenyl)dithiophosphoric acid. The reactions of 2,4-diorganyl-1,3,2,4-dithiadiphosphetane-2,4-disulfides with carvacrol (thymol) trimethylsilyl ether yield the S-trimethylsilyl esters of the corresponding dithiophosphoric acids
Dithiophosphorylation of nerol and geraniol trimethylsilyl derivatives
Get PDF漏 2017, Pleiades Publishing, Ltd.Reaction of tetraphosphorus decasulfide with 袨-(cis- and trans-3,7-dimethylocta-2,6-dien-1-yl)-trimethylsilanes affords 袨,袨-bis(cis- and trans-3,7-dimethylocta-2,6-dien-1-yl) S-(trimethylsilyl)dithiophosphates
