{"title":"黄素致敏光脱氢和光脱羧的共价中间体。","authors":"W R Knappe, P Hemmerich","doi":"10.1515/znb-1972-0907","DOIUrl":null,"url":null,"abstract":"The photoreactions of the flavin triplet with unsaturated hydrocarbons, aldehydes, sulphur compounds, and carbonic acids are reported. These reactions proceed by attack at the allylic C-H-, the RCO-H-, or the α-C-H-bond, respectively; in the case of carbonic acids decarboxylation occurs. In all the reported reactions covalent adducts are formed, whose structure and mode of decay is characterized.","PeriodicalId":78857,"journal":{"name":"Zeitschrift fur Naturforschung. Teil B. Anorganische Chemie, organische Chemie, Biochemie, Biophysik, Biologie","volume":"27 9","pages":"1032-5"},"PeriodicalIF":0.0000,"publicationDate":"1972-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1515/znb-1972-0907","citationCount":"14","resultStr":"{\"title\":\"Covalent intermediates in flavin-sensitized photodehydrogenation and photodecarboxylation.\",\"authors\":\"W R Knappe, P Hemmerich\",\"doi\":\"10.1515/znb-1972-0907\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The photoreactions of the flavin triplet with unsaturated hydrocarbons, aldehydes, sulphur compounds, and carbonic acids are reported. These reactions proceed by attack at the allylic C-H-, the RCO-H-, or the α-C-H-bond, respectively; in the case of carbonic acids decarboxylation occurs. In all the reported reactions covalent adducts are formed, whose structure and mode of decay is characterized.\",\"PeriodicalId\":78857,\"journal\":{\"name\":\"Zeitschrift fur Naturforschung. Teil B. Anorganische Chemie, organische Chemie, Biochemie, Biophysik, Biologie\",\"volume\":\"27 9\",\"pages\":\"1032-5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1972-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1515/znb-1972-0907\",\"citationCount\":\"14\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zeitschrift fur Naturforschung. Teil B. Anorganische Chemie, organische Chemie, Biochemie, Biophysik, Biologie\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1515/znb-1972-0907\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift fur Naturforschung. Teil B. Anorganische Chemie, organische Chemie, Biochemie, Biophysik, Biologie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/znb-1972-0907","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Covalent intermediates in flavin-sensitized photodehydrogenation and photodecarboxylation.
The photoreactions of the flavin triplet with unsaturated hydrocarbons, aldehydes, sulphur compounds, and carbonic acids are reported. These reactions proceed by attack at the allylic C-H-, the RCO-H-, or the α-C-H-bond, respectively; in the case of carbonic acids decarboxylation occurs. In all the reported reactions covalent adducts are formed, whose structure and mode of decay is characterized.