Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 오창호 | - |
dc.date.accessioned | 2018-03-12T06:08:14Z | - |
dc.date.available | 2018-03-12T06:08:14Z | - |
dc.date.issued | 2013-06 | - |
dc.identifier.citation | Chemistry - A European Journal. (Chemistry - A European Journal, 5 August 2013, 19(32), P.10501-10505 | en_US |
dc.identifier.issn | 0947-6539 | - |
dc.identifier.uri | http://onlinelibrary.wiley.com/doi/10.1002/chem.201301384/full | - |
dc.identifier.uri | http://hdl.handle.net/20.500.11754/45420 | - |
dc.description.abstract | A new Au-catalyzed cascade reaction was developed for the conversion of propargylic acetates 1 to benzannulated products 2 in good to excellent yields. The gold catalyst is involved in generating intermediate A and in the ene-type reaction of intermediate B for the formation of product 2 (see scheme). | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.subject | carbenes | en_US |
dc.subject | catalysis | en_US |
dc.subject | cycloisomerization | en_US |
dc.subject | ene reaction | en_US |
dc.subject | gold | en_US |
dc.subject | propargyl carboxylate | en_US |
dc.title | Gold Carbenes from Substituted Propargyl Acetates: Intramolecular Ene-type Reactions to 2-Acetoxynaphthalene Derivatives | en_US |
dc.type | Article | en_US |
dc.relation.no | 32 | - |
dc.relation.volume | 19 | - |
dc.identifier.doi | 10.1002/chem.201301384 | - |
dc.relation.page | 10501-10505 | - |
dc.relation.journal | CHEMISTRY-A EUROPEAN JOURNAL | - |
dc.contributor.googleauthor | Oh, C.H. | - |
dc.contributor.googleauthor | Kim, J.H | - |
dc.contributor.googleauthor | Piao, L. | - |
dc.contributor.googleauthor | Yu, J. | - |
dc.contributor.googleauthor | Kim, S.Y | - |
dc.relation.code | 2013009401 | - |
dc.sector.campus | S | - |
dc.sector.daehak | COLLEGE OF NATURAL SCIENCES[S] | - |
dc.sector.department | DEPARTMENT OF CHEMISTRY | - |
dc.identifier.pid | changho | - |
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