dc.citation.endPage |
4834 |
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dc.citation.number |
30 |
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dc.citation.startPage |
4831 |
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dc.citation.title |
TETRAHEDRON LETTERS |
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dc.citation.volume |
34 |
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dc.contributor.author |
LEE, E |
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dc.contributor.author |
TAE, JS |
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dc.contributor.author |
LEE, C |
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dc.contributor.author |
Park, Cheol-Min |
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dc.date.accessioned |
2023-12-22T13:06:27Z |
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dc.date.available |
2023-12-22T13:06:27Z |
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dc.date.created |
2014-11-10 |
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dc.date.issued |
1993-07 |
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dc.description.abstract |
Beta-alkoxyacrylates were found to be exceptionally efficient radical acceptors in radical-mediated intramolecular cyclizations. For example, reaction of 5-bromo-2-pentanol with ethyl propiolate, tributylstannane-mediated radical cyclization, and hydrolysis yielded (+/-)-(cis-6-methyltetrahydropyran-2-yl)acetic acid, a known component of civet. |
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dc.identifier.bibliographicCitation |
TETRAHEDRON LETTERS, v.34, no.30, pp.4831 - 4834 |
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dc.identifier.doi |
10.1016/S0040-4039(00)74101-3 |
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dc.identifier.issn |
0040-4039 |
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dc.identifier.scopusid |
2-s2.0-0027302923 |
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dc.identifier.uri |
https://scholarworks.unist.ac.kr/handle/201301/8577 |
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dc.identifier.url |
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0027302923 |
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dc.identifier.wosid |
A1993LN88200028 |
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dc.language |
영어 |
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dc.publisher |
PERGAMON-ELSEVIER SCIENCE LTD |
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dc.title |
BETA-ALKOXYACRYLATES IN RADICAL CYCLIZATIONS - REMARKABLY EFFICIENT OXACYCLE SYNTHESIS |
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dc.type |
Article |
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dc.description.journalRegisteredClass |
scopus |
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