Pure and Applied Chemistry

CrossRef Cited-by Linking

• Arribas Inmaculada, Álvarez Eleuterio, Pizzano Antonio: Novel Bis(1,3,2-diazaphospholidine) Ligands for Asymmetric Catalysis. Organometallics 2013, 32, 2497. <http://dx.doi.org/10.1021/om400185q>
• Magano Javier, Dunetz Joshua R.: Large-Scale Carbonyl Reductions in the Pharmaceutical Industry. Org. Process Res. Dev. 2012, 16, 1156. <http://dx.doi.org/10.1021/op2003826>
• Wilckens Kristina, Duhs Marcel-Antoine, Lentz Dieter, Czekelius Constantin: Chiral 1,1′-Bi(tetrahydroisoquinoline)-Type Diamines as Efficient Ligands for Nickel-Catalysed Enantioselective Michael Addition to Nitroalkenes. Eur J Org Chem 2011, 2011, 5441. <http://dx.doi.org/10.1002/ejoc.201100488>
• Wolf Christian, Xu Hanhui: Asymmetric catalysis with chiral oxazolidine ligands. Chem Commn 2011, 47, 3339. <http://dx.doi.org/10.1039/c0cc04629a>
• Wetzel Alexander, Pratsch Gerald, Kolb Roman, Heinrich Markus R.: Radical Arylation of Phenols, Phenyl Ethers, and Furans. Chem Eur J 2010, 16, 2547. <http://dx.doi.org/10.1002/chem.200902927>
• Preetz Angelika, Drexler Hans-Joachim, Fischer Christian, Dai Zhenya, Börner Armin, Baumann Wolfgang, Spannenberg Anke, Thede Richard, Heller Detlef: Rhodium-Complex-Catalyzed Asymmetric Hydrogenation: Transformation of Precatalysts into Active Species. Chem Eur J 2008, 14, 1445. <http://dx.doi.org/10.1002/chem.200701150>
• Holz Jens, Zayas Odalys, Jiao Haijun, Baumann Wolfgang, Spannenberg Anke, Monsees Axel, Riermeier Thomas H., Almena Juan, Kadyrov Renat, Börner Armin: A Highly Tunable Family of Chiral Bisphospholanes for Rh-Catalyzed Enantioselective Hydrogenation Reactions. Chem Eur J 2006, 12, 5001. <http://dx.doi.org/10.1002/chem.200600033>
• Aguado Gemma P., Rúa Federico, Branchadell Vicenç, Nielsen Peter E., Ortuño Rosa M.: Cyclobutyl-carbonyl substituted PNA: synthesis and study of a novel PNA derivative. Tet Asymm 2006, 17, 2499. <http://dx.doi.org/10.1016/j.tetasy.2006.09.012>
• Yan Yongjun, Zhang Xumu: Six-membered bis(azaphosphorinane), readily available ligand for highly enantioselective asymmetric hydrogenations. Tetrahetron Lett 2006, 47, 1567. <http://dx.doi.org/10.1016/j.tetlet.2006.01.003>
• Cluzeau Jérôme, Lubell William D.: Design, synthesis, and application of azabicyclo[X.Y.0]alkanone amino acids as constrained dipeptide surrogates and peptide mimics. Biopolymers (Biospectroscopy) 2005, 80, 98. <http://dx.doi.org/10.1002/bip.20213>
• Li Ming, Tang Dianyong, Luo Xiaoling, Shen Wei: Mechanism of asymmetric hydrogenation of enamides with [Rh(BisP*)]+ catalyst: Model DFT study. Int J Quantum Chem 2005, 102, 53. <http://dx.doi.org/10.1002/qua.20294>
• González-Arellano Camino, Corma Avelino, Iglesias Marta, Sánchez Felix: Enantioselective hydrogenation of alkenes and imines by a gold catalyst. Chem Commun 2005, 3451. <http://dx.doi.org/10.1039/b505271h>
• Wu Shulin, He Minsheng, Zhang Xumu: Synthesis of ortho-phenyl substituted MeO-BIPHEP ligand and its application in Rh-catalyzed asymmetric hydrogenation. Tet Asymm 2004, 15, 2177. <http://dx.doi.org/10.1016/j.tetasy.2004.05.043>
• Pfaltz A., Drury W. J.: Asymmetric Catalysis Special Feature Part II: Design of chiral ligands for asymmetric catalysis: From C2-symmetric P,P- and N,N-ligands to sterically and electronically nonsymmetrical P,N-ligands. Proceedings of the National Academy of Sciences 2004, 101, 5723. <http://dx.doi.org/10.1073/pnas.0307152101>
• Aguado Gemma P., Moglioni Albertina G., Brousse Beatriz N., Ortuño Rosa M.: Synthesis and diastereoselective catalytic hydrogenation of optically active cyclobutyl α,β-dehydro-α-dipeptides. Tet Asymm 2003, 14, 2445. <http://dx.doi.org/10.1016/S0957-4166(03)00485-3>
• Ireland Tania, Tappe Katja, Grossheimann Gabi, Knochel Paul: Synthesis of a New Class of Chiral 1,5-Diphosphanylferrocene Ligands and Their Use in Enantioselective Hydrogenation. Chem Eur J 2002, 8, 843. <http://dx.doi.org/10.1002/1521-3765(20020215)8:4<843::AID-CHEM843>3.0.CO;2-9>
• Lotz Matthias, Polborn Kurt, Knochel Paul: New Ferrocenyl Ligands with Broad Applications in Asymmetric Catalysis. Angew Chem 2002, 114, 4902. <http://dx.doi.org/10.1002/ange.200290023>
• Lotz Matthias, Polborn Kurt, Knochel Paul: New Ferrocenyl Ligands with Broad Applications in Asymmetric Catalysis. Angew Chem Int Ed 2002, 41, 4708. <http://dx.doi.org/10.1002/anie.200290024>
• Ishii Akihiro, Kanai Masatomi, Higashiyama Kimio, Mikami Koichi: Practical asymmetric synthetic route to 4,4,4-trifluoro-3-hydroxybutyrate: Head-to-tail and head-to-head crystallizations through double and single hydrogen bonds of hetero- and homochiral 4,4,4-trifluoro-3-hydroxybutyrophenones. Chirality 2002, 14, 709. <http://dx.doi.org/10.1002/chir.10040>
• Benincori T., Rizzo S., Sannicò F.: Free design of chiral diphosphine chelating ligands for stereoselective homogeneous catalysis by assmbling five-membered atomatic heterocycles. J Heterocyclic Chem 2002, 39, 471. <http://dx.doi.org/10.1002/jhet.5570390304>
• Madec J, Pfister X, Phansavath P, Ratovelomanana-Vidal V, Genêt J.-P: Asymmetric hydrogenation reactions using a practical in situ generation of chiral ruthenium–diphosphine catalysts from anhydrous RuCl3. Tetrahedron 2001, 57, 2563. <http://dx.doi.org/10.1016/S0040-4020(01)00067-9>
• Saylik Dilek, Campi Eva M., Donohue Andrew C., Jackson W.Roy, Robinson Andrea J.: A new enantioselective synthesis of β-amino acids. Tet Asymm 2001, 12, 657. <http://dx.doi.org/10.1016/S0957-4166(01)00097-0>
• Franciò Giancarlo, Faraone Felice, Leitner Walter: Von Chinolin abgeleitete, chirale Phosphan/Phosphoramidit-Liganden (QUINAPHOS) für die asymmetrische Katalyse. Angew Chem 2000, 112, 1486. <http://dx.doi.org/10.1002/(SICI)1521-3757(20000417)112:8<1486::AID-ANGE1486>3.0.CO;2-B>
• Jiang Qiongzhong, Xiao Dengming, Zhang Zhaoguo, Cao Ping, Zhang Xumu: Hochenantioselektive Hydrierung cyclische Enolacetate mit einem Rhodium-PennPhos-Komplex. Angew Chem 1999, 111, 578. <http://dx.doi.org/10.1002/(SICI)1521-3757(19990215)111:4<578::AID-ANGE578>3.0.CO;2-N>
• Ireland Tania, Großheimann Gabriele, Wieser-Jeunesse Catherine, Knochel Paul: Ferrocenylliganden mit zwei Phosphanylsubstituenten inα,ɛ-Position für die Übergangsmetall-katalysierte asymmetrische Hydrierung funktionalisierter Doppelbindungen. Angew Chem 1999, 111, 3397. <http://dx.doi.org/10.1002/(SICI)1521-3757(19991102)111:21<3397::AID-ANGE3397>3.0.CO;2-R>
• Jones Stephen W., Palmer Christopher F., Paul Jane M., Tiffin Peter D.: Preparation of (S)-2-quinolylalanine by asymmetric hydrogenation. Tetrahetron Lett 1999, 40, 1211. <http://dx.doi.org/10.1016/S0040-4039(98)02568-4>
• Yamano Toru, Taya Naohiro, Kawada Mitsuru, Huang Taisheng, Imamoto Tsuneo: Enantioselective hydrogenation of β-keto esters catalyzed by P-chiral bis(dialkylphosphino)ethanes-Ru(II). Tetrahetron Lett 1999, 40, 2577. <http://dx.doi.org/10.1016/S0040-4039(99)00251-8>
• Burk Mark J., Bedingfield Karen M., Kiesman William F., Allen John G.: Catalytic asymmetric hydrogenation of β-substituted α,β,γ,δ-unsaturated amino acids. Tetrahetron Lett 1999, 40, 3093. <http://dx.doi.org/10.1016/S0040-4039(99)00437-2>
• Stammers Timothy A., Burk Mark J.: Synthesis of enantiomerically pure backbone alkyl substituted peptide nucleic acids utilizing the Et-DuPHOS-Rh+ hydrogenation of enamido esters. Tetrahetron Lett 1999, 40, 3325. <http://dx.doi.org/10.1016/S0040-4039(99)00518-3>
• Holz Jens, Heller Detlef, Stürmer Rainer, Börner Armin: Synthesis of the first water-soluble chiral tetrahydroxy diphosphine Rh(I) catalyst for enantioselective hydrogenation. Tetrahetron Lett 1999, 40, 7059. <http://dx.doi.org/10.1016/S0040-4039(99)01458-6>
• Jiang Qiongzhong, Jiang Yutong, Xiao Dengming, Cao Ping, Zhang Xumu: Hoch enantioselektive Hydrierung einfacher Ketone mit PennPhos-Rh-Katalysatoren. Angew Chem 1998, 110, 1203. <http://dx.doi.org/10.1002/(SICI)1521-3757(19980420)110:8<1203::AID-ANGE1203>3.0.CO;2-M>
• Fehring Volker, Selke Rüdiger: Hochenantioselektive komplexkatalysierte Reduktion von Ketonen – jetzt auch mit rein aliphatischen Derivaten. Angew Chem 1998, 110, 1927. <http://dx.doi.org/10.1002/(SICI)1521-3757(19980703)110:13/14<1927::AID-ANGE1927>3.0.CO;2-I>
• Burk Mark J., Bienewald Frank, Harris Michael, Zanotti-Gerosa Antonio: Einfacher Zugang zu 2-Alkylsuccinaten durch asymmetrische katalytische Hydrierung von durch Stobbe-Kondensation erhaltenen Itaconaten. Angew Chem 1998, 110, 2034. <http://dx.doi.org/10.1002/(SICI)1521-3757(19980703)110:13/14<2034::AID-ANGE2034>3.0.CO;2-C>
• Hegedus Louis S.: Transition metals in organic synthesis: highlights for the year 1996. Coord Chem Rev - 1998, 168, 49. <http://dx.doi.org/10.1016/S0010-8545(97)00067-2>
• Hoerrner R. Scott, Askin David, Volante R.P., Reider Paul J.: A highly enantioselective asymmetric hydrogenation route to β-(2R,3S)-methyltryptophan. Tetrahetron Lett 1998, 39, 3455. <http://dx.doi.org/10.1016/S0040-4039(98)00604-2>
• Burk Mark J., Allen John G., Kiesman William F., Stoffan Karen M.: A convenient cross-coupling route to α,β,γ,δ-unsaturated amino acids. Tetrahetron Lett 1997, 38, 1309. <http://dx.doi.org/10.1016/S0040-4039(97)00065-8>
• Davies David T., Goodall Karen, Kapur Neha, O'Brien Matthew, Parsons Andrew F.: The Synthesis of Dehydroamino Acids from Pyruvic Acid. Synth Common 1997, 27, 3815. <http://dx.doi.org/10.1080/00397919708007306>