Pure and Applied Chemistry

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• Wang Xiaoming, Guo Peihua, Han Zhaobin, Wang Xubin, Wang Zheng, Ding Kuiling: Spiroketal-Based Diphosphine Ligands in Pd-Catalyzed Asymmetric Allylic Amination of Morita–Baylis–Hillman Adducts: Exceptionally High Efficiency and New Mechanism. J. Am. Chem. Soc. 2014, 136, 405. <http://dx.doi.org/10.1021/ja410707q>
• Nishioka Noriyuki, Koizumi Toshio: Pd(0)-catalyzed polycondensation of aryl-substituted propargylic carbonates with bifunctional nucleophiles promoted by aryl group on the acetylenic terminal carbon. J Polym Sci A Polym Chem 2011, 49, 642. <http://dx.doi.org/10.1002/pola.24475>
• Dai Li, Li Xin, Yuan Hao, Li Xia, Li Zhihuai, Xu Di, Fei Fan, Liu Yingqiang, Zhang Jun, Zhou Zhiming: Ionic-salt-tagged ferrocenyl diphosphine–imine ligands and their application to palladium-catalyzed asymmetric allylic etherification. Tet Asymm 2011, 22, 1379. <http://dx.doi.org/10.1016/j.tetasy.2011.07.025>
• Zhang Ping, Le Hai, Kyne Robert E., Morken James P.: Enantioselective Construction of All-Carbon Quaternary Centers by Branch-Selective Pd-Catalyzed Allyl–Allyl Cross-Coupling. J Am Chem Soc 2011, 133, 9716. <http://dx.doi.org/10.1021/ja2039248>
• Wang Yu, Hämäläinen Antti, Tois Jan, Franzén Robert: Preparation of indole-phosphine oxazoline (IndPHOX) ligands and their application in allylic alkylation. Tet Asymm 2010, 21, 2376. <http://dx.doi.org/10.1016/j.tetasy.2010.08.008>
• Saporita Maria, Bottari Giovanni, Bruno Giuseppe, Drommi Dario, Faraone Felice: Regio- and enantioselectivity in the alkylation and etherification reactions of cinnamyl allylic derivatives catalyzed by [(η5-C5R5)Ru(N–N*)(NCCH3)]PF6 (R=H, Me) complexes containing N–N* bulky chiral ligands of different rigidity and flexibility. Journal of Molecular Catalysis A 2009, 309, 159. <http://dx.doi.org/10.1016/j.molcata.2009.05.011>
• Kadnikova Ekaterina N., Thakor Vikalp A.: Enantioselective hydrolysis of 1-arylallyl acetates catalyzed by Candida antarctica lipase. Tet Asymm 2008, 19, 1053. <http://dx.doi.org/10.1016/j.tetasy.2008.04.018>
• Foltz Carole, Enders Markus, Bellemin-Laponnaz Stéphane, Wadepohl Hubert, Gade Lutz H.: Using a Tripod as a Chiral Chelating Ligand: Chemical Exchange Between Equivalent Molecular Structures in Palladium Catalysis with 1,1,1-Tris(oxazolinyl)ethane (“Trisox”). Chem Eur J 2007, 13, 5994. <http://dx.doi.org/10.1002/chem.200700307>
• Gavrilov Konstantin N., Maksimova Marina G., Zheglov Sergey V., Bondarev Oleg G., Benetsky Eduard B., Lyubimov Sergey E., Petrovskii Pavel V., Kabro Anzhelika A., Hey-Hawkins Evamarie, Moiseev Sergey K.: Ferrocenyliminophosphites as Easy-to-Modify Ligands for Asymmetric Catalysis. Eur J Org Chem 2007, 2007, 4940. <http://dx.doi.org/10.1002/ejoc.200700396>
• Trost Barry M., Horne Daniel B., Woltering Michael J.: Palladium-Catalyzed DYKAT of Butadiene Monoepoxide: Enantioselective Total Synthesis of (+)-DMDP, (−)-Bulgecinine, and (+)-Broussonetine G. Chem Eur J 2006, 12, 6607. <http://dx.doi.org/10.1002/chem.200600202>
• Mikhel Igor S., Bernardinelli Gérald, Alexakis Alexandre: Chiral P-monodentate phosphoramidite and phosphite ligands for the enantioselective Pd-catalyzed allylic alkylation. Inorg Chim Ada 2006, 359, 1826. <http://dx.doi.org/10.1016/j.ica.2005.06.040>
• Diéguez Montserrat, Pàmies Oscar, Claver Carmen: Furanoside thioether–phosphinite ligands for Pd-catalyzed asymmetric allylic substitution reactions: Scope and limitations. J Organomet Chem 2006, 691, 2257. <http://dx.doi.org/10.1016/j.jorganchem.2005.11.024>
• Trudeau Stéphane, Morken James P.: StePHOX, a new family of optically active, tunable phosphine–oxazoline ligands: syntheses and applications. Tetrahedron 2006, 62, 11470. <http://dx.doi.org/10.1016/j.tet.2006.05.043>
• Hilgraf Robert, Pfaltz Andreas: Chiral Bis(N-sulfonylamino)phosphine- and TADDOL-Phosphite-Oxazoline Ligands: Synthesis and Application in Asymmetric Catalysis. Adv Synth Catal 2005, 347, 61. <http://dx.doi.org/10.1002/adsc.200404168>
• Gouriou Laure, Lloyd-Jones Guy C, Vyskočil Štěpán, Kočovský Pavel: 2H-quadrupolar coupling-based analysis of stereochemical and regiochemical memory in the Pd-catalysed allylic alkylation of iso-cinnamyl type substrates employing the chiral monophosphine ligands ‘MOP’ and ‘MAP’. J Organomet Chem 2003, 687, 525. <http://dx.doi.org/10.1016/j.jorganchem.2003.09.015>
• Carmona Daniel, Ferrer Joaquina, Lalaguna Elena, Lorenzo Mónica, Lahoz Fernando J., Elipe Sergio, Oro Luis A.: Preparation and Properties of RhI and IrI Ethylene Complexes Containing the ChiralP,N-Chelate Ligand (4S)-2-[2-(Diphenylphosphanyl)phenyl]-4-isopropyl-1,3-oxazoline. Eur J Inorg Chem 2002, 2002, 259. <http://dx.doi.org/10.1002/1099-0682(20021)2002:1<259::AID-EJIC259>3.0.CO;2-T>
• Dotta Pascal, Anil Kumar P. G., Pregosin Paul S.: A [Pd (η3-PhCHCHCHPh)(phosphino-oxazoline)]+ complex with almost identical P- and N-trans influences.13C chemical shifts and allylic alkylation chemistry. Magn Reson Chem 2002, 40, 653. <http://dx.doi.org/10.1002/mrc.1075>
• van Haaren Richard J, Keeven Peter H, van der Veen Lars A, Goubitz Kees, van Strijdonck Gino P.F, Oevering Henk, Reek Joost N.H, Kamer Paul C.J, van Leeuwen Piet W.N.M: The effect of ligand donor atoms on the regioselectivity in the palladium catalyzed allylic alkylation. Inorg Chim Ada 2002, 327, 108. <http://dx.doi.org/10.1016/S0020-1693(01)00694-6>
• van Haaren Richard J., van Strijdonck Gino P. F., Oevering Henk, Reek Joost N. H., Kamer Paul C. J., van Leeuwen Piet W. N. M.: On the Influence of the Bite Angle on the Allylic Alkylation of (E) and (Z) Substrates: Loss and Retention of Double Bond Stereochemistry. Eur J Inorg Chem 2001, 2001, 837. <http://dx.doi.org/10.1002/1099-0682(200103)2001:3<837::AID-EJIC837>3.0.CO;2-J>
• Tanabe Keisuke, Takeuchi Ryo: Highly Regioselective Allylic Alkylation of Dienyl Acetates and Enynyl Acetates Catalyzed by an Iridium Complex. Angew Chem 2000, 112, 2051. <http://dx.doi.org/10.1002/1521-3757(20000602)112:11<2051::AID-ANGE2051>3.0.CO;2-S>
• Polosukhin A.I, Gavrilov K.N, Bondarev O.G, Korostylev A.V, Petrovskii P.V, Davankov V.A: Quincoridine-based aminophosphite ligands and their Rh(I) and Pd(II) complexes. J Organomet Chem 2000, 608, 89. <http://dx.doi.org/10.1016/S0022-328X(00)00373-9>
• Takeuchi Ryo: Iridium complex-catalyzed allylic alkylation. J Polyhedron 2000, 19, 557. <http://dx.doi.org/10.1016/S0277-5387(99)00407-6>
• Gavrilov Konstantin N, Polosukhin Aleksei I: Chiral P,N-bidentate ligands in coordination chemistry and organic catalysis involving rhodium and palladium. RUSS CHEM REV 2000, 69, 661. <http://dx.doi.org/10.1070/RC2000v069n08ABEH000559>
• Lukešová Lenka, Ludvík Jiří, Císařová Ivana, Štěpnička Petr: Group 6 Metal Mixed Carbonyl Complexes with a Carboxyferrocenylphosphane. Collect Czech Chem Commun 2000, 65, 1897. <http://dx.doi.org/10.1135/cccc20001897>
• Pfaltz Andreas: Chiral heterocycles as ligands in asymmetric catalysis. J Heterocyclic Chem 1999, 36, 1437. <http://dx.doi.org/10.1002/jhet.5570360607>
• Meynhardt B., Lüning U., Wolff C., Näther C.: Diastereoselective Generation of Quaternary Stereocenters by Ligand-Controlled Palladium-Catalyzed Allylations. Eur J Org Chem 1999, 1999, 2327. <http://dx.doi.org/10.1002/(SICI)1099-0690(199909)1999:9<2327::AID-EJOC2327>3.0.CO;2-H>