Matches in SemOpenAlex for { <https://semopenalex.org/work/W2953354919> ?p ?o ?g. }
- W2953354919 endingPage "637" @default.
- W2953354919 startingPage "571" @default.
- W2953354919 abstract "Molecular oxygen constitutes about one fifth of the global atmospheric air, and hence, it is one of the most abundant and inexpensive natural resources, and can be utilized as a very useful reagent in synthetic organic chemistry. Because the electronic configuration of the oxygen molecule acquires a triplet state in the ground state, it is involved in radical type reactions, such as autoxidation of benzylic positions. Additionally, by very simple modifications, it can be transformed into ozone, singlet oxygen or peroxides, all of which are excellent synthetic reagents as well. Thus, ozone adds to, by 1,3-dipolar cycloaddition, and cleaves carbon–carbon double bonds under very mild conditions. Singlet oxygen however reacts with various olefins mostly in three modes. It adds to 1,3-dienes by the Diels-Alder type mechanism, and gives such cyclic peroxides as ascaridol. In the case of sterically hindered and electron rich olefins, a 1,2-cycloaddition reaction will take place and unstable dioxetane can be obtained." @default.
- W2953354919 created "2019-06-27" @default.
- W2953354919 creator A5066039132 @default.
- W2953354919 date "1995-01-01" @default.
- W2953354919 modified "2023-09-25" @default.
- W2953354919 title "Biogenesis-like transformation of 4-substituted phenols by photooxygenation" @default.
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