Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0957-4166(99)00117-2
DC FieldValue
dc.titleA versatile and efficient approach to enantiomerically pure monodentate and bidentate P-chiral phosphines
dc.contributor.authorLeung, P.-H.
dc.contributor.authorLiu, A.
dc.contributor.authorMok, K.F.
dc.date.accessioned2014-06-23T05:31:09Z
dc.date.available2014-06-23T05:31:09Z
dc.date.issued1999-04-09
dc.identifier.citationLeung, P.-H., Liu, A., Mok, K.F. (1999-04-09). A versatile and efficient approach to enantiomerically pure monodentate and bidentate P-chiral phosphines. Tetrahedron Asymmetry 10 (7) : 1309-1314. ScholarBank@NUS Repository. https://doi.org/10.1016/S0957-4166(99)00117-2
dc.identifier.issn09574166
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75502
dc.description.abstractEnantiomerically pure (R)-methylphenylvinylphosphine and the P-chiral diphosphine ligands (5R,7R)-, (5R,7S)- and (5S,7R)-[5- (methylphenylphosphino)-2,3-dimethyl-7-phenyl-7-phosphabicyclo[2.2.1]hept-2- ene] were stereospecifically obtained in high yields from the chiral palladium template controlled Diels-Alder reaction between (±)- methylphenylphosphine and 3,4-dimethylphenylphosphole.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0957-4166(99)00117-2
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/S0957-4166(99)00117-2
dc.description.sourcetitleTetrahedron Asymmetry
dc.description.volume10
dc.description.issue7
dc.description.page1309-1314
dc.description.codenTASYE
dc.identifier.isiut000080466500009
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