A highly efficient synthesis of (S)-(+)-N-Boc-coniine using ring-closing olefin metathesis (RCM)
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Jo, E | ko |
| dc.contributor.author | Na, Y | ko |
| dc.contributor.author | Chang, Sukbok | ko |
| dc.date.accessioned | 2013-03-02T21:22:52Z | - |
| dc.date.available | 2013-03-02T21:22:52Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1999-07 | - |
| dc.identifier.citation | TETRAHEDRON LETTERS, v.40, no.30, pp.5581 - 5582 | - |
| dc.identifier.issn | 0040-4039 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/75584 | - |
| dc.description.abstract | Optically active (S)-(+)-coniine as an N-Boc protected form was concisely prepared starting from an amino acid, L-norvaline. The key step involved a ring-closing olefin metathesis (RCM) of the dialkenyl compound 6 to give the corresponding cyclic olefin 8 in an essentially quantitative yield. (C) 1999 Elsevier Science Ltd. All rights reserved. | - |
| dc.language | English | - |
| dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
| dc.subject | PIPERIDINE ALKALOIDS | - |
| dc.subject | ORGANIC-SYNTHESIS | - |
| dc.title | A highly efficient synthesis of (S)-(+)-N-Boc-coniine using ring-closing olefin metathesis (RCM) | - |
| dc.type | Article | - |
| dc.identifier.wosid | 000081427400037 | - |
| dc.type.rims | ART | - |
| dc.citation.volume | 40 | - |
| dc.citation.issue | 30 | - |
| dc.citation.beginningpage | 5581 | - |
| dc.citation.endingpage | 5582 | - |
| dc.citation.publicationname | TETRAHEDRON LETTERS | - |
| dc.identifier.doi | 10.1016/S0040-4039(99)01081-3 | - |
| dc.contributor.localauthor | Chang, Sukbok | - |
| dc.contributor.nonIdAuthor | Jo, E | - |
| dc.contributor.nonIdAuthor | Na, Y | - |
| dc.type.journalArticle | Article | - |
| dc.subject.keywordPlus | PIPERIDINE ALKALOIDS | - |
| dc.subject.keywordPlus | ORGANIC-SYNTHESIS | - |
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