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Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol© 2016, Pleiades Publishing, Ltd.Carvacrol trimethylsilyl ether when reacting with P4S10 forms S

Chiral salts of dithiophosphoric acids on the basis of organic nitrogen compounds

Chiral S-stannyl dithiophosphates and dithiophosphonates on the basis of monoterpenolsCopyright © 2018 John Wiley & Sons, Ltd. Chiral S-tributylstannyl dithiophosphates

Novel effectively carbonaceous and sulfurated hydrogen corrosion inhibitors on the basis of organosulfurphosphorus compounds white phosphorus, elemental sulfur, industrial alcohols or phenols, and amines. Long-chain S-alkyl O

α-d-Glucofuranose and α-d-allofuranose diacetonides and silyl ether of α-d-glucofuranose diacetonide in dithiophosphorylation reactions of n-hexadecylamine. The S-silyldithiophosphonate was prepared in 93% yield by the reaction of 2,4-bis

Cinchona Alkaloids in the Synthesis of Chiral Salts of Phosphorus Dithioacids on the Basis of 1,2:3,4-Di-O-isopropylidene-α-D-galactopyranose and dithiophosphonic acids with 8 S,9R-quinine, 8R,9 S-quinidine, 8 S,9R-cinchonidine, 8R,9 S-cinchonine, and 8R,9 S

Disilyl dithiophosphonates in the synthesis of open chain and cyclic organothiophosphorus compoundsO-(Trimethylsiloxy)alkyl S-trimethylsilyl aryldithiophosphonates 7a-d were obtained by the reaction

Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol© 2016, Pleiades Publishing, Ltd.Carvacrol trimethylsilyl ether when reacting with P4S10 forms S

Dithiophosphonation of 4-(1H-pyrrol-1-yl)phenol and 4-(1H-imidazol-1-yl)phenol

Long-chain alkyl esters of O,O-dialkyl dithiophosphoric and thionophosphoric acids prepared on the basis of red phosphorus, elemental sulfur, alcohols, and industrial fractions of higher monoolefinsCopyright © Taylor & Francis Group, LLC. Mixtures of long chain S-alkyl O

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