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Oxygen, heterocyclic compounds 1,3-dioxolane

Calculation of group increments for oxygen, sulfur and nitrogen compounds has allowed the estimation of conventional ring-strain energies (CRSE) for saturated heterocycles from enthalpies of formation. For 1,3-dioxolane, CRSE is about 20 kJ mol . In 2,4-dialkyl-l,3-dioxolanes the cis form is always thermodynamically the more stable by approximately 1 kJ mol" . [Pg.32]


See other pages where Oxygen, heterocyclic compounds 1,3-dioxolane is mentioned: [Pg.102]    [Pg.1091]    [Pg.21]    [Pg.336]    [Pg.258]    [Pg.297]   
See also in sourсe #XX -- [ Pg.494 ]




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Compounds oxygenated

Heterocycle oxygen

Heterocycles oxygenation

Heterocyclic compounds 1,3-dioxolane

Heterocyclic oxygen

Heterocyclics 1.3- dioxolanes

Oxygen compounds

Oxygen heterocycles compounds

Oxygen heterocyclic compounds

Oxygenate compounds

Oxygenous compound

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