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The reaction of lead tetra-acetate with some unbranched α,ω-diols
(Elsevier, 1969)
Unbranched α,ω-diols are mainly converted by means of lead tetra-acetate in refluxing benzene to the corresponding ethers of di-α-tetrahydrofuryl, di-α-tetrahydropyryl and/or α-tetrahydrofuryl-α′-tetrahydropyryl type. Thus, ...
Reactions with lead tetraacetate-I. Oxidation of saturated aliphatic alcohols part 1
(Elsevier, 1964)
When oxidized with lead tetraacetate 1-heptanol and 1-octanol undergo cyclization to give as major products the corresponding 2-alkyltetrahydrofurans, accompanied by a small amount of the isomeric tetrahydropyran derivatives. ...
Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers
(Elsevier, 1965)
The lead tetraacetate oxidation of saturated aliphatic alcohols, with structures which do not permit 1,5-cyclization, gave tetrahydropyran derivatives in yields not exceeding 16%. The formation of a small amount of the ...
Opening of steroid ring a by means of lead tetraacetate
(Elsevier, 1964)
The lead tetraacetate oxidation of cholestan-1β-ol and cholestan-1α-ol in benzene solution did not afford cyclic ethers but resulted, in major part, in the opening of ring A with formation of 1,10-seco-aldehydes. In addition, ...
The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate
(Elsevier, 1965)
The only amino compounds oxidized so far with lead tetroacetate were primary aromatic amines, which gave mainly the corresponding azo compounds(1), and some tertiary aryldialkyl amines, which in glacial acetic acid in the ...
Reactions with lead tetraacetate. I. Oxidation of saturated aliphatic alcohols. Part 1
(Elsevier, 1963)
It was recently shown that various steroid alcohols could react with lead tetraacetate in non-polar solvents to give tetrahydrofuran and tetrahydropyran derivatives. cyclization occurring when the position of and the ...