REDUCTIVE RING-OPENING OF CYCLOPROPYL KETONES WITH SAMARIUM(II) DIIODIDE
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Yong Hae | ko |
| dc.contributor.author | LEE, IS | ko |
| dc.date.accessioned | 2013-02-25T09:31:30Z | - |
| dc.date.available | 2013-02-25T09:31:30Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1992-10 | - |
| dc.identifier.citation | HETEROATOM CHEMISTRY, v.3, no.5-6, pp.509 - 512 | - |
| dc.identifier.issn | 1042-7163 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/61189 | - |
| dc.description.abstract | Functionalized cyclopropyl ketones have been found to undergo facile reductive cyclopropane ring opening with samarium (II) diiodide in the presence of a proton source. These reactions were exceedingly rapid, taking place in most cases at -78-degrees-C under neutral conditions. An ester group substituted at the C2 position of the cyclopropane ring played an important role in the ring opening of cyclopropyl ketones. | - |
| dc.language | English | - |
| dc.publisher | JOHN WILEY & SONS INC | - |
| dc.subject | ORGANIC-SYNTHESIS | - |
| dc.title | REDUCTIVE RING-OPENING OF CYCLOPROPYL KETONES WITH SAMARIUM(II) DIIODIDE | - |
| dc.type | Article | - |
| dc.identifier.wosid | A1992KL80300009 | - |
| dc.type.rims | ART | - |
| dc.citation.volume | 3 | - |
| dc.citation.issue | 5-6 | - |
| dc.citation.beginningpage | 509 | - |
| dc.citation.endingpage | 512 | - |
| dc.citation.publicationname | HETEROATOM CHEMISTRY | - |
| dc.identifier.doi | 10.1002/hc.520030510 | - |
| dc.contributor.nonIdAuthor | LEE, IS | - |
| dc.type.journalArticle | Article | - |
| dc.subject.keywordPlus | ORGANIC-SYNTHESIS | - |
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