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Intramolecular Diels-Alder cycloadditions of 2-pyrones toward the synthesis of medium sized macrocyclic skeletons
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 조천규 | - |
| dc.date.accessioned | 2021-08-04T03:24:16Z | - |
| dc.date.available | 2021-08-04T03:24:16Z | - |
| dc.date.issued | 2006-04-20 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/70492 | - |
| 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 | 제97회-2006년 춘계대한화학회 | - |
| dc.citation.conferencePlace | 고양시한국국제전시장 | - |
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