Juliana V Petrova,Maria E Filkina,Yuri K Grishin,Vitaly A Roznyatovsky,Victor A Tafeenko,Mikhail S Nechaev,Bogdan I Ugrak,Tatyana Ya Dutova,Artemii M Savin,Arsenii Y Boldyrikhin,Maxim E Kukushkin,Elena K Beloglazkina
{"title":"腈亚胺与2-亚胺-噻唑[3,2-a]嘧啶-3-酮的1,3-偶极环加成:偶极引发的噻唑-咪唑酮重排。","authors":"Juliana V Petrova,Maria E Filkina,Yuri K Grishin,Vitaly A Roznyatovsky,Victor A Tafeenko,Mikhail S Nechaev,Bogdan I Ugrak,Tatyana Ya Dutova,Artemii M Savin,Arsenii Y Boldyrikhin,Maxim E Kukushkin,Elena K Beloglazkina","doi":"10.1021/acs.joc.5c00670","DOIUrl":null,"url":null,"abstract":"The 1,3-dipolar cycloaddition of nitrile imines to thiazolo[3,2-a]pyrimidine imines featuring both endocyclic and exocyclic C═N bonds was first reported. This reaction resulted in the regio- and stereoselective attachment of two dipole moieties, accompanied by peculiar skeletal rearrangements within the thiazolone fragment. Any products of only dipole addition cannot be isolated. The observed reactivity was explained using DFT protocols to investigate the cyclization mechanism of nitrile imines with thiazolo[3,2-a]pyrimidines.","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"39 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"1,3-Dipolar Cycloaddition of Nitrile Imines to 2-Imino-thiazolo[3,2-a]pyrimidin-3-ones: Dipole-Initiated Thiazolone-Imidazolone Rearrangement.\",\"authors\":\"Juliana V Petrova,Maria E Filkina,Yuri K Grishin,Vitaly A Roznyatovsky,Victor A Tafeenko,Mikhail S Nechaev,Bogdan I Ugrak,Tatyana Ya Dutova,Artemii M Savin,Arsenii Y Boldyrikhin,Maxim E Kukushkin,Elena K Beloglazkina\",\"doi\":\"10.1021/acs.joc.5c00670\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The 1,3-dipolar cycloaddition of nitrile imines to thiazolo[3,2-a]pyrimidine imines featuring both endocyclic and exocyclic C═N bonds was first reported. This reaction resulted in the regio- and stereoselective attachment of two dipole moieties, accompanied by peculiar skeletal rearrangements within the thiazolone fragment. Any products of only dipole addition cannot be isolated. The observed reactivity was explained using DFT protocols to investigate the cyclization mechanism of nitrile imines with thiazolo[3,2-a]pyrimidines.\",\"PeriodicalId\":57,\"journal\":{\"name\":\"Journal of Organic Chemistry\",\"volume\":\"39 1\",\"pages\":\"\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-10-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Organic Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.joc.5c00670\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.joc.5c00670","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
1,3-Dipolar Cycloaddition of Nitrile Imines to 2-Imino-thiazolo[3,2-a]pyrimidin-3-ones: Dipole-Initiated Thiazolone-Imidazolone Rearrangement.
The 1,3-dipolar cycloaddition of nitrile imines to thiazolo[3,2-a]pyrimidine imines featuring both endocyclic and exocyclic C═N bonds was first reported. This reaction resulted in the regio- and stereoselective attachment of two dipole moieties, accompanied by peculiar skeletal rearrangements within the thiazolone fragment. Any products of only dipole addition cannot be isolated. The observed reactivity was explained using DFT protocols to investigate the cyclization mechanism of nitrile imines with thiazolo[3,2-a]pyrimidines.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.