Conversion of Thionoesters and Thionolactones to Ethers; a General and Efficient Radical Desulfurisation
Triphenyltin hydride reduces thionoesters and thionolactones to their corresponding ethers in high yield.
Nicolaou, Kyriacos C.,Sato, Mitsunobu,Theodorakis, Emmanuel A.,Miller, Neil D.
p. 1583 - 1586
(2007/10/02)
A MILD PROCEDURE FOR ETHERIFICATION OF ALCOHOLS WITH PRIMARY ALKYL HALIDES IN THE PRESENCE OF SILVER TRIFLATE
Alcohols were alkylated in good to excellent yield with primary alkyl halides by a method employing silver triflate and a non-nucleophilic amine base.
Burk, Robert M.,Gac, Todd S.,Roof, Michael B.
p. 8111 - 8112
(2007/10/02)
SOLVOLYSIS OF 3β-CHLORO-5-CHOLESTENE IN THE PRESENCE OF ZINC SALTS
When heated in alcohols in the presence of zinc chloride 3β-chloro-5-cholestene undergoes solvolysis, and cholesterol ethers are formed with high yields.The same direction of reaction is preserved if the zinc chloride is formed directly in the reaction mixture.
Kutulya, L. A.,Oleinik, S. S.,Protsenko, L. I.,Tishchenko, V. G.
p. 1467 - 1469
(2007/10/02)
Reactions of relevance to the chemistry of aminoglycoside antibiotics. Part 8. Synthesis and properties of O-alkyl selenoesters.
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Barton,Hansen,Picker
p. 1723 - 1730
(2007/10/05)
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