dc.contributor.author | Louis, Ignace | |
dc.contributor.author | L. Hungerford, Natasha | |
dc.contributor.author | J. Humphries, Edward | |
dc.contributor.author | D. McLeod, Malcolm | |
dc.date.accessioned | 2017-05-03T15:25:31Z | |
dc.date.available | 2017-05-03T15:25:31Z | |
dc.date.issued | 2006 | |
dc.date.modified | 2010-01-11T07:54:46Z | |
dc.identifier.issn | 15237052 | |
dc.identifier.doi | 10.1021/ol053092b | |
dc.identifier.uri | http://hdl.handle.net/10072/28186 | |
dc.description.abstract | The enantioselective total synthesis of (-)-dactylolide is reported. The absolute stereochemistry of the tetrahydropyran was established by catalytic asymmetric Jacobsen hetero-Diels-Alder reaction. The remote C19 stereocenter was introduced by a sequence of chelation-controlled Grignard addition and Ireland-Claisen rearrangement. | |
dc.description.peerreviewed | Yes | |
dc.description.publicationstatus | Yes | |
dc.language | English | |
dc.language.iso | eng | |
dc.publisher | American Chemical Society | |
dc.publisher.place | Washington, DC | |
dc.relation.ispartofstudentpublication | N | |
dc.relation.ispartofpagefrom | 1117 | |
dc.relation.ispartofpageto | 1120 | |
dc.relation.ispartofissue | 6 | |
dc.relation.ispartofjournal | Organic Letters | |
dc.relation.ispartofvolume | 8 | |
dc.rights.retention | Y | |
dc.subject.fieldofresearch | Organic Chemical Synthesis | |
dc.subject.fieldofresearch | Chemical Sciences | |
dc.subject.fieldofresearchcode | 030503 | |
dc.subject.fieldofresearchcode | 03 | |
dc.title | Enantioselective total synthesis of (-)-dactylolide | |
dc.type | Journal article | |
dc.type.description | C1 - Articles | |
dc.type.code | C - Journal Articles | |
gro.date.issued | 2006 | |
gro.hasfulltext | No Full Text | |
gro.griffith.author | Hungerford, Natasha L. | |