Repository at Hanyang UniversityCOLLEGE OF NATURAL SCIENCES[S](자연과학대학)CHEMISTRY(화학과)Articles
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dc.contributor.author조천규-
dc.date.accessioned2019-11-29T05:07:57Z-
dc.date.available2019-11-29T05:07:57Z-
dc.date.issued2017-08-
dc.identifier.citationORGANIC LETTERS, v. 19, no. 17, page. 4688-4691en_US
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.orglett.7b02372-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/115155-
dc.description.abstractA flexible synthetic strategy for the total syntheses of ningalins D and G is described. The highly effective TMS-OTf/2,6-lutidine-mediated [3,3]-sigmatropic rearrangement of densely loaded dinaphthyl hydrazides and cyclization of the resulting 2,2'-diamino-1,1'-dinaphthyls afforded the key 7H-dibenzo[c,g]carbazole intermediates. Successful conversions to biphenylene quinone methides followed by regioselective brominations completed the total syntheses of the titled marine alkaloids.en_US
dc.description.sponsorshipThis work was supported by the grants from the National Research Foundation of Korea (2014R1A5A1011165).en_US
dc.language.isoen_USen_US
dc.publisherAMER CHEMICAL SOCen_US
dc.subjectFISCHER INDOLE SYNTHESISen_US
dc.subjectMETHYL ARENESen_US
dc.subjectALKALOIDSen_US
dc.subjectREARRANGEMENTen_US
dc.subjectHYDRAZIDESen_US
dc.subjectACIDen_US
dc.subjectBROMINATIONen_US
dc.subjectLAMELLARINSen_US
dc.subjectCOMBINATIONen_US
dc.subjectIODINATIONen_US
dc.titleTotal Syntheses of Ningalins D and Gen_US
dc.typeArticleen_US
dc.relation.no17-
dc.relation.volume19-
dc.identifier.doi10.1021/acs.orglett.7b02372-
dc.relation.page4688-4691-
dc.relation.journalORGANIC LETTERS-
dc.contributor.googleauthorKim, Jang-Yeop-
dc.contributor.googleauthorKim, Dong-Hyun-
dc.contributor.googleauthorJeon, Tae-Hong-
dc.contributor.googleauthorKim, Woo-Hyung-
dc.contributor.googleauthorCho, Cheon-Gyu-
dc.relation.code2017001238-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidccho-
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