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dc.contributor.author민선준-
dc.date.accessioned2019-05-22T01:21:30Z-
dc.date.available2019-05-22T01:21:30Z-
dc.date.issued2018-02-
dc.identifier.citationORGANIC LETTERS, v. 20, No. 4, Page. 1175-1178en_US
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.orglett.8b00098-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/105362-
dc.description.abstractA concise synthesis of 8-azabicyclo [3.2.1] octanes via sequential oxidative Mannich reactions is described. This approach involves an intermolecular oxidative Mannich coupling reaction between N-aryl pyrrolidines with TMS enol ether and a subsequent intramolecular oxidative Mannich cyclization of the corresponding silyl enol ether. DDQ is used as a key oxidant for both reactions.en_US
dc.description.sponsorshipThis work was supported by the National Research Foundation of Korea (NRF-2016R1A2B1012277 and 2014M3C1A3054141) and the Korea Health Industry Development Institute (KHIDI, HI17C1037).en_US
dc.language.isoen_USen_US
dc.publisherAMER CHEMICAL SOCen_US
dc.subjectCATALYTIC ENANTIOSELECTIVE SYNTHESISen_US
dc.subjectDEHYDROGENATIVE COUPLING REACTIONSen_US
dc.subjectBOND-FORMING REACTIONSen_US
dc.subjectC-H FUNCTIONALIZATIONen_US
dc.subjectTROPANE ALKALOIDSen_US
dc.subjectASYMMETRIC-SYNTHESISen_US
dc.subjectTERTIARY-AMINESen_US
dc.subjectAEROBIC CONDITIONSen_US
dc.subjectDERIVATIVESen_US
dc.subjectPHOTOREDOXen_US
dc.titleConstruction of 8-Azabicyclo[3.2.1]octanes via Sequential DDQ-Mediated Oxidative Mannich Reactions of N-Aryl Pyrrolidinesen_US
dc.typeArticleen_US
dc.relation.no4-
dc.relation.volume20-
dc.identifier.doi10.1021/acs.orglett.8b00098-
dc.relation.page1175-1178-
dc.relation.journalORGANIC LETTERS-
dc.contributor.googleauthorJo, Hanbyeol-
dc.contributor.googleauthorHassan, Ahmed H. E.-
dc.contributor.googleauthorJung, Seung Young-
dc.contributor.googleauthorLee, Jae Kyun-
dc.contributor.googleauthorCho, Yong Seo-
dc.contributor.googleauthorMin, Sun-Joon-
dc.relation.code2018001077-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY[E]-
dc.sector.departmentDEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING-
dc.identifier.pidsjmin-


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