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Pyrolysis azetidine

The thermodynamics and shock-tube kinetics of pyrolysis of azetidine, in argon at high dilution, have been compared with those for trimethylene oxide, sulfide and imine. ... [Pg.405]

In the present review the ring systems containing one heteroatom are considered first, except for P-lactams which are given a special section at the end. Interest in azetidines continues to be stimulated by the discovery of the potentially useful trinitro derivative. The requirements for the stereoselective synthesis of substituted oxetane are being explored and derivatives of aluminium are useful in the stereoselective routes to oxetanones. The preparation and subsequent pyrolysis of oxetanones is suggested as an alternative to the Wittig route to olefins. Stereoselective routes to thietanes and thietane 1 -oxides are mentioned. [Pg.66]


See other pages where Pyrolysis azetidine is mentioned: [Pg.239]    [Pg.269]    [Pg.703]    [Pg.176]    [Pg.239]    [Pg.269]    [Pg.239]    [Pg.269]    [Pg.398]    [Pg.703]    [Pg.703]    [Pg.239]    [Pg.269]    [Pg.5]    [Pg.703]    [Pg.84]    [Pg.61]   
See also in sourсe #XX -- [ Pg.405 ]

See also in sourсe #XX -- [ Pg.405 ]




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Azetidine

Azetidines pyrolysis

Azetidines pyrolysis

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