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Intramolecular Diels-Alder cycloadditions of 2-pyrones toward the synthesis of medium sized macrocyclic skeletons.
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 조천규 | - |
| dc.date.accessioned | 2021-08-04T02:52:10Z | - |
| dc.date.available | 2021-08-04T02:52:10Z | - |
| dc.date.issued | 2006-06-26 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/69823 | - |
| dc.description.abstract | Synthesis of medium-sized macrolactones via an intramolecular Diels-Alder (IMDA) reaction of 2-pyrone containing alkyne tether occurs with remarkably high diastereofacial as well as endo/exo selectivity. Because of the ring strain in the alkyne-tethered, medium-sized ring system, single methyl group provides sufficient steric bias leading to the formation of single diastereomeric medium-sized macrolactones. | - |
| dc.title | Intramolecular Diels-Alder cycloadditions of 2-pyrones toward the synthesis of medium sized macrocyclic skeletons. | - |
| dc.type | Conference | - |
| dc.citation.conferenceName | 18th International Symposium on Chirality | - |
| dc.citation.conferencePlace | 부산해운대그랜드호텔 | - |
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Collections - 서울 자연과학대학 > 서울 화학과 > 2. Conference Papers
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Related Researcher
- Cho, Cheon Gyu
- COLLEGE OF NATURAL SCIENCES (DEPARTMENT OF CHEMISTRY)