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Four-membered heterocycles photochemistry

Saturated three- and four-membered heterocyclics absorb little in the readily accessible regions of the UV spectrum. Sulfur-containing rings are an exception, as can be seen in Table 9, Despite the lack of absorption of most parent compounds, there is a wealth of photochemistry of small heterocyclics. Light absorption by substituents, and energy transfer from photoexcited molecules present in the photoreactive system make photoconversion of the heterocycles practical. On the other hand, the lack of substantial absorption of their own can be exploited in the preparation of small heterocycles, by designing the system to be unsuitable for destructive energy transfer. [Pg.153]

The aromaticity of three- and four-membered cyclic sulphur compounds has been discussed as part of an overall review of aromaticity in heterocyclic compounds. The photochemistry of organic sulphur compounds, including reactions involving small rings, has been reviewed. ... [Pg.186]


See other pages where Four-membered heterocycles photochemistry is mentioned: [Pg.12]    [Pg.12]    [Pg.12]    [Pg.12]    [Pg.880]    [Pg.880]    [Pg.935]    [Pg.172]   
See also in sourсe #XX -- [ Pg.11 , Pg.11 ]




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