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   <subfield code="a">[2+2]-Photocycloaddition von Cyclohexen an 2-Acetyl-5,5-dimethyl-1,3-cyclohexandion und 3-Acetyl-1,5,5-trimethyl-2,4-pyrrolidindion</subfield>
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   <subfield code="a">[2+2]-Photocycloaddition of cyclohexene to 2-acetyl-5,5-dimethyl-1,3-cyclohexanedione and 3-acetyl-1,5,5-trimethyl-2,4-pyrrolidinedion</subfield>
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   <subfield code="a">Summary: Irradiation of solutions of excess cyclohexene and 2-acetyl-5,5-dimethyl-1,3-cyclohexanedione (1), and 3-acetyl-1,5,5-trimethyl-2,4-pyrrolidinedione (4) results mainly in the formation of 1,5-diones2 and5. These originate from intermediate cycloadducts of cyclohexene and theexo-enols of the cyclic 1,3-diketones. The yields decrease with increasing polarity of the solvent. In solution2 and5 are in equilibrium with the cyclic hemiacetales3 and6.</subfield>
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