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Sulfoxides acylation

Dimethyl sulfoxide See Dimethyl sulfoxide Acyl halides... [Pg.280]

A mixture of the (highly activated) dichloro compound with potassium fluoride in the solvent was heated to reflux to effect replacement of chlorine by fluorine. The reaction accelerated out of control and exploded, leaving much carbonised residue. Analogous reactions had been effected uneventfully on many previous occasions. See Dimethyl sulfoxide Acyl halides, etc. [Pg.669]

Occasionally, departures from these considerations have been made where such action appeared advantageous in bringing out a relationship between formally unrelated compounds or hazards. In all multi-component cases, however, the secondary reactants (except air and water) appear as formula entries back-referred to the main entry text, so that the latter is accessible from either primary or secondary reactants. See Dimethyl sulfoxide Acyl halides (main entry)... [Pg.2118]


See other pages where Sulfoxides acylation is mentioned: [Pg.237]    [Pg.872]    [Pg.1439]    [Pg.1441]    [Pg.1453]    [Pg.1456]    [Pg.1463]    [Pg.1538]    [Pg.263]    [Pg.312]    [Pg.756]    [Pg.943]    [Pg.1480]    [Pg.1483]    [Pg.1489]    [Pg.1490]    [Pg.1505]    [Pg.1508]    [Pg.1516]    [Pg.1601]    [Pg.230]    [Pg.872]    [Pg.1439]    [Pg.1441]    [Pg.1453]    [Pg.1456]    [Pg.1463]    [Pg.1538]    [Pg.230]   
See also in sourсe #XX -- [ Pg.155 ]




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Acyl halides with sulfoxides

Acylation of dimethyl sulfoxide

Acylation of the sulfoxide

Acylation of the sulfoxide oxygen

Sulfoxides a-alkylthio, as acyl anion equivalent

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