|1.||Utsunomiya, Masaru: 2 articles (10/2009 - 02/2006)|
|2.||Incarvito, Christopher D: 2 articles (07/2006 - 02/2006)|
|3.||Hartwig, John F: 2 articles (07/2006 - 02/2006)|
|4.||van Leeuwen, P W: 2 articles (11/2001 - 08/2001)|
|5.||Huang, Hanmin: 1 article (09/2015)|
|6.||Yu, Hui: 1 article (09/2015)|
|7.||Zhang, Guoying: 1 article (09/2015)|
|8.||Nakahara, Yasuhito: 1 article (10/2009)|
|9.||Miyamoto, Yoshiki: 1 article (10/2009)|
|10.||Ohshima, Takashi: 1 article (10/2009)|
|1.||Bites and Stings (Sting)
09/07/2015 - "[Pd(Xantphos)I2 ], which features a very large bite angle, has been found to facilitate the rapid carbonylation of azaarene-substituted allylamines into bioactive quinolizinones in good to excellent yields. "
07/19/2006 - "The rate and yield were higher from the complex ligated by Xantphos, which contains a larger bite angle. "
02/15/2006 - "The catalyst for these reactions is generated from [Pd(eta(3)-allyl)Cl](2) (with or without added AgOTf) or [Pd(CH(3)CN)(4)](BF(4))(2) and Xantphos (9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene), which generates complexes with large P-Pd-P bite angles. "
08/20/2004 - "The reaction is strongly influenced by the presence of nBu4NCl, and the use of Xantphos, a rigid bidentate ligand with a wide natural bite angle, was found to be crucial for the success of the reaction. "
02/15/2006 - "Studies of substituted unsymmetrical and unsubstituted symmetrical model eta(3)-allyl complexes showed that nucleophilic attack on complexes ligated by Xantphos was faster than on complexes bearing ligands with smaller bite angles and that nucleophilic attack on unsymmetrical allyl complexes with larger bite angle ligands was faster than on unsymmetrical allyl complexes with smaller bite angle ligands. "
|2.||2-naphthol BINAP (BINAP)
|9.||allyl alcohol (allylic alcohol)