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Methyl chlorosulfite

Pritchard and co-workers (147) reported the preparation of an acyclic chiral sulfite, 98, which is formed as a mixture of diastereo-mers in the reaction between racemic methyl chlorosulfite and (+)-diphenacyl malate. The pure diastereomers of 98 were isolated by fractional crystallization. [Pg.364]

Dehydration Alumina (see also Dihydropyrane, preparation). Boric acid. Boron triSuoride. N-Bromoacetamide-Pyridine-SOj. Dicyclohexylcarbodiimide. Diketene. Dimethylform-amide-Thionyl chloride. Dimethyl sulfoxide. Ethylene chlorophosphite. Florisil. Girard s reagent. Hydrobromic acid. Iodine. Mesyl chloride-Sulfur dioxide. Methyl chlorosulfite. Methylketene diethylacetal. Naphthalene-d-sulfonic acid. Oxalic acid. Phenyl isocyanate. Phosgene. Phosphorus pentoxide. Phosphoryl chloride. Phthalic anhydride. Potassium bisulfate. Pyridine. Thionyi chloride. Thoria. p-Toluenesulfonic acid. p-Toluenesulfonyl chloride. Triphenylphosphine dibromide. [Pg.1387]

Polymerization at subzero temperatures initiated by methyl chlorosulfite and hydroperoxide [231]. [Pg.272]

Hexadiynylene chlorosulfite, 2155 Lithium ethynediolate, 0989 f Methoxyacetylene, 1143 3-Methoxypropyne, 1520 f Methyl propiolate, 1438... [Pg.2209]

See other pages where Methyl chlorosulfite is mentioned: [Pg.619]    [Pg.198]    [Pg.198]    [Pg.619]    [Pg.619]    [Pg.198]    [Pg.198]    [Pg.619]    [Pg.489]    [Pg.399]    [Pg.1315]    [Pg.65]   
See also in sourсe #XX -- [ Pg.675 ]



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Chlorosulfite

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