Enone–alkene Cycloadditions
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Enone–alkene Cycloadditions
In organic chemistry, enone–alkene cycloadditions are a version of the +2cycloaddition This reaction involves an enone and alkene as substrates. Although the concerted photochemical +2cycloaddition is allowed, the reaction between enones and alkenes is stepwise and involves discrete diradical intermediates. History In 1908, it was reported that exposure of carvone to "Italian sunlight" for one year gives carvone- camphor. Subsequent investigations demonstrated the utility of the photochemical +2cycloaddition of enones to alkenes. Mechanism In spite of the stepwise, radical mechanism, both stereoselective intra- and intermolecular variants have emerged. Cyclic enones are employed, otherwise competitive cis-trans isomerization ensues. The mechanism of +2photocyclization is proposed to begin with photoexcitation of the enone to a singlet excited state. The singlet state is typically very short lived, and decays by intersystem crossing to the triplet state. At this point, ...
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Organic Chemistry
Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms.Clayden, J.; Greeves, N. and Warren, S. (2012) ''Organic Chemistry''. Oxford University Press. pp. 1–15. . Study of structure determines their structural formula. Study of properties includes physical and chemical properties, and evaluation of chemical reactivity to understand their behavior. The study of organic reactions includes the chemical synthesis of natural products, drugs, and polymers, and study of individual organic molecules in the laboratory and via theoretical ( in silico) study. The range of chemicals studied in organic chemistry includes hydrocarbons (compounds containing only carbon and hydrogen) as well as compounds based on carbon, but also containing other elements, especially oxygen, nitrogen, sulfur, phosphorus (included in ...
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