Aryl Hydrazides to Indoles and Synthesis of Indolo[3,2-b]carbozole
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 조천규 | - |
dc.date.accessioned | 2021-08-03T21:32:51Z | - |
dc.date.available | 2021-08-03T21:32:51Z | - |
dc.date.issued | 20090820 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/61172 | - |
dc.description.abstract | Aryl hydrazides underwent the Fischer indolization reactions, while the N-carbamate group(s) remained intact to directly provide N-Cbzindoles. This new method allowed the synthesis of various N-Cbz-carbazoles and N,N′-bis-Cbz-pyrrolo[2,3-f]indoles. | - |
dc.title | Aryl Hydrazides to Indoles and Synthesis of Indolo[3,2-b]carbozole | - |
dc.type | Conference | - |
dc.citation.conferenceName | 2009 대한화학회 유기화학분과회 | - |
dc.citation.conferencePlace | 강원, 설악한화콘도 | - |
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