dc.contributor.authorZou, Yinjun
dc.contributor.authorQin, Liena
dc.contributor.authorRen, Xinfeng
dc.contributor.authorLu, Yunpeng
dc.contributor.authorLi, Yongxin
dc.contributor.authorZhou, Jianrong Steve
dc.date.accessioned2014-04-04T06:01:34Z
dc.date.available2014-04-04T06:01:34Z
dc.date.copyright2013en_US
dc.date.issued2013
dc.identifier.citationZou, Y., Qin, L., Ren, X., Lu, Y., Li, Y., & Zhou, J. S. (2013). Selective Arylation and Vinylation at the α Position of Vinylarenes. Chemistry - A European Journal, 19(10), 3504-3511.en_US
dc.identifier.issn0947-6539en_US
dc.identifier.urihttp://hdl.handle.net/10220/19097
dc.description.abstractIn intermolecular Heck reactions of styrene and vinylarenes, the aryl and vinyl groups routinely insert at the β position. However, selective insertion at the α position has been very rare. Herein, we provide a missing piece in the palette of Heck reaction, which gave >20:1 α selectivity. The key to our success is a new ferrocene 1,1′-bisphosphane (dnpf) that carries 1-naphthyl groups. Our mechanistic studies revealed that the high α selectivity is partly attributable to the steric effect of dnpf. The rigid and bulky 1-naphthyl groups of dnpf sterically disfavor β insertion.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesChemistry - A European Journalen_US
dc.rights© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds
dc.titleSelective Arylation and Vinylation at the α Position of Vinylarenesen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1002/chem.201203646


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record