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New Synthetic Routes to (+)-Uleine and (-)-Tubifolidine: General Approach to 2-Azabicyclo[3.3.1]nonane Indole Alkaloids
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Dong-Hyun | - |
| dc.contributor.author | Kim, Jeong-Hwa | - |
| dc.contributor.author | Jeon, Tae-Hong | - |
| dc.contributor.author | Cho, Cheon-Gyu | - |
| dc.date.accessioned | 2022-07-08T03:30:35Z | - |
| dc.date.available | 2022-07-08T03:30:35Z | - |
| dc.date.created | 2021-05-12 | - |
| dc.date.issued | 2020-05 | - |
| dc.identifier.issn | 1523-7060 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/145729 | - |
| dc.description.abstract | Novel asymmetric synthetic routes to (+)-uleine and (-)-tubifolidine are reported herein. The regioselective formation of enol triflates from 2-azabicyclo[3.3.1]nonane ketones followed by indolizations of the resultant ene-hydrazides allowed the efficient construction of key indole intermediates, facilitating the total synthesis of the target natural alkaloids. | - |
| dc.language | 영어 | - |
| dc.language.iso | en | - |
| dc.publisher | AMER CHEMICAL SOC | - |
| dc.title | New Synthetic Routes to (+)-Uleine and (-)-Tubifolidine: General Approach to 2-Azabicyclo[3.3.1]nonane Indole Alkaloids | - |
| dc.type | Article | - |
| dc.contributor.affiliatedAuthor | Cho, Cheon-Gyu | - |
| dc.identifier.doi | 10.1021/acs.orglett.0c00912 | - |
| dc.identifier.scopusid | 2-s2.0-85083311810 | - |
| dc.identifier.wosid | 000530076400032 | - |
| dc.identifier.bibliographicCitation | ORGANIC LETTERS, v.22, no.9, pp.3464 - 3468 | - |
| dc.relation.isPartOf | ORGANIC LETTERS | - |
| dc.citation.title | ORGANIC LETTERS | - |
| dc.citation.volume | 22 | - |
| dc.citation.number | 9 | - |
| dc.citation.startPage | 3464 | - |
| dc.citation.endPage | 3468 | - |
| dc.type.rims | ART | - |
| dc.type.docType | Article | - |
| dc.description.journalClass | 1 | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.subject.keywordPlus | FORMAL TOTAL-SYNTHESIS | - |
| dc.subject.keywordPlus | ENANTIOSELECTIVE TOTAL SYNTHESES | - |
| dc.subject.keywordPlus | CATALYTIC ASYMMETRIC-SYNTHESIS | - |
| dc.subject.keywordPlus | STRYCHNOS ALKALOIDS | - |
| dc.subject.keywordPlus | FISCHER INDOLIZATION | - |
| dc.subject.keywordPlus | FUNCTIONALIZED 2-AZABICYCLO< | - |
| dc.subject.keywordPlus | 3.3.1> | - |
| dc.subject.keywordPlus | NONANES | - |
| dc.subject.keywordPlus | AKUAMMILINE ALKALOIDS | - |
| dc.subject.keywordPlus | ENTRY | - |
| dc.subject.keywordPlus | (-)-STRYCHNINE | - |
| dc.subject.keywordPlus | (+)-ASPIDOSPERMIDINE | - |
| dc.identifier.url | https://pubs.acs.org/doi/10.1021/acs.orglett.0c00912 | - |
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Related Researcher
- Cho, Cheon Gyu
- COLLEGE OF NATURAL SCIENCES (DEPARTMENT OF CHEMISTRY)