Arianna Bini, Prof. Mariella Mella, Prof. Daniele Merli, Prof. Stefano Protti
{"title":"封面:光化学与热酸催化的大麻萜醇(CBG)环化:意想不到的选择性(ChemPhotoChem 11/2024)","authors":"Arianna Bini, Prof. Mariella Mella, Prof. Daniele Merli, Prof. Stefano Protti","doi":"10.1002/cptc.202481101","DOIUrl":null,"url":null,"abstract":"<p><b>The Front Cover</b> highlights investigations of the reactivity of Cannabigerol (CBG) in organic solvents under both photochemical and acid catalyzed conditions, pointing out the key role of the photoexcited CBG* in the selective formation of a 2,2-disubstituted-chromane derivative (green path). On the other hand, in the presence of Brønsted-Lowry acids, two tertiary carbocations are competitively generated (I<sup>+</sup>, II<sup>+</sup>, orange and blue paths). Finally, when performing the reaction in toluene in the presence of BF<sub>3</sub>*OEt<sub>2</sub>, a Friedel Crafts-like alkylation of the solvent was noticed (purple paths). More information can be found in the Research Article by Daniele Merli, Stefano Protti, and co-workers (DOI: 10.1002/cptc.202400157).\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure>\n </p>","PeriodicalId":10108,"journal":{"name":"ChemPhotoChem","volume":"8 11","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cptc.202481101","citationCount":"0","resultStr":"{\"title\":\"Front Cover: Photochemical Vs Thermal Acid Catalysed Cyclization of Cannabigerol (CBG): An Unexpected Selectivity (ChemPhotoChem 11/2024)\",\"authors\":\"Arianna Bini, Prof. Mariella Mella, Prof. Daniele Merli, Prof. Stefano Protti\",\"doi\":\"10.1002/cptc.202481101\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><b>The Front Cover</b> highlights investigations of the reactivity of Cannabigerol (CBG) in organic solvents under both photochemical and acid catalyzed conditions, pointing out the key role of the photoexcited CBG* in the selective formation of a 2,2-disubstituted-chromane derivative (green path). On the other hand, in the presence of Brønsted-Lowry acids, two tertiary carbocations are competitively generated (I<sup>+</sup>, II<sup>+</sup>, orange and blue paths). Finally, when performing the reaction in toluene in the presence of BF<sub>3</sub>*OEt<sub>2</sub>, a Friedel Crafts-like alkylation of the solvent was noticed (purple paths). More information can be found in the Research Article by Daniele Merli, Stefano Protti, and co-workers (DOI: 10.1002/cptc.202400157).\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure>\\n </p>\",\"PeriodicalId\":10108,\"journal\":{\"name\":\"ChemPhotoChem\",\"volume\":\"8 11\",\"pages\":\"\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-11-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cptc.202481101\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemPhotoChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cptc.202481101\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemPhotoChem","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cptc.202481101","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Front Cover: Photochemical Vs Thermal Acid Catalysed Cyclization of Cannabigerol (CBG): An Unexpected Selectivity (ChemPhotoChem 11/2024)
The Front Cover highlights investigations of the reactivity of Cannabigerol (CBG) in organic solvents under both photochemical and acid catalyzed conditions, pointing out the key role of the photoexcited CBG* in the selective formation of a 2,2-disubstituted-chromane derivative (green path). On the other hand, in the presence of Brønsted-Lowry acids, two tertiary carbocations are competitively generated (I+, II+, orange and blue paths). Finally, when performing the reaction in toluene in the presence of BF3*OEt2, a Friedel Crafts-like alkylation of the solvent was noticed (purple paths). More information can be found in the Research Article by Daniele Merli, Stefano Protti, and co-workers (DOI: 10.1002/cptc.202400157).