DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hong, Seonghyeok | ko |
dc.contributor.author | Kweon, Byeongseok | ko |
dc.contributor.author | Lee, Wooseok | ko |
dc.contributor.author | Chang, Sukbok | ko |
dc.contributor.author | Hong, Sungwoo | ko |
dc.date.accessioned | 2023-05-17T02:00:40Z | - |
dc.date.available | 2023-05-17T02:00:40Z | - |
dc.date.created | 2023-05-02 | - |
dc.date.created | 2023-05-02 | - |
dc.date.created | 2023-05-02 | - |
dc.date.issued | 2023-04 | - |
dc.identifier.citation | ORGANIC LETTERS, v.25, no.15, pp.2722 - 2727 | - |
dc.identifier.issn | 1523-7060 | - |
dc.identifier.uri | http://hdl.handle.net/10203/306876 | - |
dc.description.abstract | A one-pot umpolung method for the ring-opening pyridylation of unstrained cyclic amines was developed using N-amidopyridinium salts. This process involves the formation of electron donor-acceptor complexes between bromide and N-amidopyridinium salts, ultimately leading to the functionalization of pyridines. This protocol is compatible with a range of 5-or 6-membered cyclic amines and pyridines, thereby providing a powerful synthon for preparing C4functionalized pyridines under visible-light conditions in the absence of an external photocatalyst. | - |
dc.language | English | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.title | Deconstructive Pyridylation of Unstrained Cyclic Amines through a One-Pot Umpolung Approach | - |
dc.type | Article | - |
dc.identifier.wosid | 000970557300001 | - |
dc.identifier.scopusid | 2-s2.0-85152663585 | - |
dc.type.rims | ART | - |
dc.citation.volume | 25 | - |
dc.citation.issue | 15 | - |
dc.citation.beginningpage | 2722 | - |
dc.citation.endingpage | 2727 | - |
dc.citation.publicationname | ORGANIC LETTERS | - |
dc.identifier.doi | 10.1021/acs.orglett.3c00922 | - |
dc.contributor.localauthor | Chang, Sukbok | - |
dc.contributor.localauthor | Hong, Sungwoo | - |
dc.description.isOpenAccess | N | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordPlus | TERTIARY-AMINES | - |
dc.subject.keywordPlus | LIGHT | - |
dc.subject.keywordPlus | FUNCTIONALIZATION | - |
dc.subject.keywordPlus | RADICALS | - |
dc.subject.keywordPlus | NITROGEN | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.