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The photooxygenation of the 1-methyl-, 2,3-dimethyl-, and 1,4-dimethylcyclohexa-1,4-dienes, which are readily available through Birch reduction, yielded the corresponding ene-products. The formed endocyclic dienes were trapped by the addition of sing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3688fc40dd752e0f562a20bac042730
https://avesis.erciyes.edu.tr/publication/details/adfe399b-ee2b-4e53-981b-dd21166e576e/oai
https://avesis.erciyes.edu.tr/publication/details/adfe399b-ee2b-4e53-981b-dd21166e576e/oai
