Silver-Promoted Site-Selective Intramolecular Cyclization of 2-Methylthiobenzamide Through α-C(sp3)–H Functionalization
dc.contributor.author | Yang, Ke | |
dc.contributor.author | Niu, Ben | |
dc.contributor.author | Ma, Zhiyan | |
dc.contributor.author | Wang, Hui | |
dc.contributor.author | Lawrence, Brianna | |
dc.contributor.author | Ge, Haibo | |
dc.contributor.department | Chemistry and Chemical Biology, School of Science | en_US |
dc.date.accessioned | 2019-12-23T16:06:27Z | |
dc.date.available | 2019-12-23T16:06:27Z | |
dc.date.issued | 2019-11 | |
dc.description.abstract | Silver-mediated intramolecular α-C(sp3)–H bond functionalization of the methylthio group has been established in the presence of Selectfluor as an additive. This novel strategy provides efficient access to various diverse sulfur-based heterocycles with good yields and functional group compatibility. It is noteworthy that the completely novel benzooxathiin-4-imine skeletons were reported for the first time in this study. | en_US |
dc.eprint.version | Author's manuscript | en_US |
dc.identifier.citation | Yang, K., Niu, B., Ma, Z., Wang, H., Lawrence, B., & Ge, H. (2019). Silver-promoted site-selective intramolecular cyclization of 2-methylthiobenzamide through α-C(sp3)–H functionalization. The Journal of Organic Chemistry. https://doi.org/10.1021/acs.joc.9b02202 | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/21560 | |
dc.language.iso | en | en_US |
dc.publisher | ACS | en_US |
dc.relation.isversionof | 10.1021/acs.joc.9b02202 | en_US |
dc.relation.journal | The Journal of Organic Chemistry | en_US |
dc.rights | Publisher Policy | en_US |
dc.source | Author | en_US |
dc.subject | transition metal-promoted α-C–H bond functionalization | en_US |
dc.subject | sulfide group | en_US |
dc.title | Silver-Promoted Site-Selective Intramolecular Cyclization of 2-Methylthiobenzamide Through α-C(sp3)–H Functionalization | en_US |
dc.type | Article | en_US |