dc.contributor.author | Aumann, Kylee M | |
dc.contributor.author | Healy, Peter C | |
dc.contributor.author | Coster, Mark J | |
dc.date.accessioned | 2017-05-03T15:16:52Z | |
dc.date.available | 2017-05-03T15:16:52Z | |
dc.date.issued | 2011 | |
dc.date.modified | 2012-02-14T05:30:20Z | |
dc.identifier.issn | 0040-4039 | |
dc.identifier.doi | 10.1016/j.tetlet.2010.12.076 | |
dc.identifier.uri | http://hdl.handle.net/10072/42572 | |
dc.description.abstract | Attempts to selectively arylate [6,6]-spiroacetal enol ethers at the 2-position delivered unexpected results. Palladium-mediated arylation conditions afforded the double-Heck product, whereas reaction with benzenesulfinic acid resulted in a facile rearrangement into the corresponding 5-phenylsulfonyl-3,4,5,6-tetrahydrochromans, providing access to 5-aryl-3,4,5,6-tetrahydrochroman and hexahydrochroman derivatives. | |
dc.description.peerreviewed | Yes | |
dc.description.publicationstatus | Yes | |
dc.language | English | |
dc.language.iso | eng | |
dc.publisher | Elsevier | |
dc.publisher.place | United Kingdom | |
dc.relation.ispartofstudentpublication | N | |
dc.relation.ispartofpagefrom | 1070 | |
dc.relation.ispartofpageto | 1073 | |
dc.relation.ispartofissue | 10 | |
dc.relation.ispartofjournal | Tetrahedron Letters | |
dc.relation.ispartofvolume | 52 | |
dc.rights.retention | Y | |
dc.subject.fieldofresearch | Medicinal and biomolecular chemistry | |
dc.subject.fieldofresearch | Organic chemistry | |
dc.subject.fieldofresearch | Organic chemical synthesis | |
dc.subject.fieldofresearchcode | 3404 | |
dc.subject.fieldofresearchcode | 3405 | |
dc.subject.fieldofresearchcode | 340503 | |
dc.title | Arylation of [6,6]-spiroacetal enol ethers: reactivity and rearrangement | |
dc.type | Journal article | |
dc.type.description | C1 - Articles | |
dc.type.code | C - Journal Articles | |
gro.date.issued | 2011 | |
gro.hasfulltext | No Full Text | |
gro.griffith.author | Healy, Peter C. | |