ENANTIOSELECTIVE EPOXIDATION OF CYCLIC 1,3-DIENES CATALYZED BY A STERICALLY AND ELECTRONICALLY OPTIMIZED (SALEN)MN COMPLEX
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Chang, Sukbok | ko |
| dc.contributor.author | HEID, RM | ko |
| dc.contributor.author | JACOBSEN, EN | ko |
| dc.date.accessioned | 2013-02-25T18:09:34Z | - |
| dc.date.available | 2013-02-25T18:09:34Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1994-01 | - |
| dc.identifier.citation | TETRAHEDRON LETTERS, v.35, no.5, pp.669 - 672 | - |
| dc.identifier.issn | 0040-4039 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/64207 | - |
| dc.description.abstract | Chiral (salen)Mn(m)Cl complexes catalyze epoxidation of cyclic 1,3-dienes with moderate-to-good enantioselectivity. A new catalyst (2), bearing sterically hindered and electron donating OSi(iPr)(3) (OTIPS)substituents, induces up to 12% higher selectivity than the previously-reported tert-butyl substituted analog 1. | - |
| dc.language | English | - |
| dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
| dc.subject | EPOXIDES | - |
| dc.title | ENANTIOSELECTIVE EPOXIDATION OF CYCLIC 1,3-DIENES CATALYZED BY A STERICALLY AND ELECTRONICALLY OPTIMIZED (SALEN)MN COMPLEX | - |
| dc.type | Article | - |
| dc.identifier.wosid | A1994MU47700004 | - |
| dc.type.rims | ART | - |
| dc.citation.volume | 35 | - |
| dc.citation.issue | 5 | - |
| dc.citation.beginningpage | 669 | - |
| dc.citation.endingpage | 672 | - |
| dc.citation.publicationname | TETRAHEDRON LETTERS | - |
| dc.identifier.doi | 10.1016/S0040-4039(00)75786-8 | - |
| dc.contributor.localauthor | Chang, Sukbok | - |
| dc.contributor.nonIdAuthor | HEID, RM | - |
| dc.contributor.nonIdAuthor | JACOBSEN, EN | - |
| dc.type.journalArticle | Article | - |
| dc.subject.keywordPlus | EPOXIDES | - |
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