Pure and Applied Chemistry

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• Busacca Carl A., Qu Bo, Grět Nicole, Fandrick Keith R., Saha Anjan K., Marsini Maurice, Reeves Diana, Haddad Nizar, Eriksson Magnus, Wu Jiang-Ping, Grinberg Nelu, Lee Heewon, Li Zhibin, Lu Bruce, Chen Dajun, Hong Yaping, Ma Shengli, Senanayake Chris H.: Tuning the Peri Effect for Enantioselectivity: Asymmetric Hydrogenation of Unfunctionalized Olefins with the BIPI Ligands. Adv. Synth. Catal. 2013, 355, 1455. <http://dx.doi.org/10.1002/adsc.201201104>
• Gutmann Torsten, del Rosal Iker, Chaudret Bruno, Poteau Romuald, Limbach Hans-Heinrich, Buntkowsky Gerd: From Molecular Complexes to Complex Metallic Nanostructures- 2 H Solid-State NMR Studies of Ruthenium-Containing Hydrogenation Catalysts. ChemPhysChem 2013, 14, 3026. <http://dx.doi.org/10.1002/cphc.201300200>
• Busacca Carl A., Fandrick Daniel R., Song Jinhua J., Senanayake Chris H.: The Growing Impact of Catalysis in the Pharmaceutical Industry. Synth Catal 2011, 353, 1825. <http://dx.doi.org/10.1002/adsc.201100488>
• Heckenroth Marion, Khlebnikov Vsevolod, Neels Antonia, Schurtenberger Peter, Albrecht Martin: Catalytic Hydrogenation Using Abnormal N-Heterocyclic Carbene Palladium Complexes: Catalytic Scope and Mechanistic Insights. ChemCatChem 2011, 3, 167. <http://dx.doi.org/10.1002/cctc.201000270>
• Schurig Volker: Gas chromatographic enantioseparation of derivatized α-amino acids on chiral stationary phases—Past and present. J Chromatogr B 2011, 879, 3122. <http://dx.doi.org/10.1016/j.jchromb.2011.04.005>
• Gopalaiah Kovuru, Kagan Henri B.: Use of Nonfunctionalized Enamides and Enecarbamates in Asymmetric Synthesis. Chemistry Review 2011, 111, 4599. <http://dx.doi.org/10.1021/cr100031f>
• Kagan H. B., Fiaud J. C., Hoornaert C., Meyer D., Poulin J. C.: Synthesis of new chiral phosphines for asymmetric catalysis. Bull Soc Chim Belges 2010, 88, 923. <http://dx.doi.org/10.1002/bscb.19790881113>
• Asymmetrische Hydrierungen. Nachr Chem Tech Lab 2010, 25, 712. <http://dx.doi.org/10.1002/nadc.19770251212>
• Achamlale S., Mabrouk H., Elachqar A., El Hallaoui A., El Hajji S., Alami A., Bellan J., Mazières M. R., Wolf J. G., Pierrot M.: Synthesis and Thermal Isomerization of Carboxylic and Phosphonic α-Aminoesters Substituted With a Triazole Ring. Phosphorus Sulfur Silicon Relat Elem 2007, 182, 357. <http://dx.doi.org/10.1080/10426500600919959>
• Brunner Henri: Rhodium-Katalysatoren für die enantioselektive Hydrosilylierung - ein neues Konzept zur Entwicklung asymmetrischer Katalysatoren. Angew Chem 2006, 95, 921. <http://dx.doi.org/10.1002/ange.19830951202>
• Berens Ulrich, Englert Ulli, Geyser Stefan, Runsink Jan, Salzer Albrecht: A Flexible Approach to Different Families of Bidentate P,P Ligands as Highly Efficient Ligands for Asymmetric Catalysis. Eur J Org Chem 2006, 2006, 2100. <http://dx.doi.org/10.1002/ejoc.200500937>
• Kagan Henri B: Various aspects of the reaction of a chiral catalyst or reagent with a racemic or enantiopure substrate. Tetrahedron 2001, 57, 2449. <http://dx.doi.org/10.1016/S0040-4020(01)00065-5>
• Kobayashi Kimiko, Kato Takayuki, Unno Masafumi, Masuda Shinji: Asymmetric Synthesis of Organosilicon Compounds Using a C2 Chiral Auxiliary. Bull Chem Soc Jpn 1997, 70, 1393. <http://dx.doi.org/10.1246/bcsj.70.1393>
• Kotha Sambasivarao: Opportunities in asymmetric synthesis: An industrial prospect. Tetrahedron 1994, 50, 3639. <http://dx.doi.org/10.1016/S0040-4020(01)90388-6>
• Genet J.P., Pinel C., Mallart S., Juge S., Thorimbert S., Laffitte J.A.: Asymmetric synthesis. Practical production of D and L threonine. Dynamic kinetic resolution in rhodium and ruthenium catalyzed hydrogenation of 2-acylamino-3-oxobutyrates. Tet Asymm 1991, 2, 555. <http://dx.doi.org/10.1016/S0957-4166(00)86108-X>
• Braun Manfred, Moritz Jörg: (S,S)-1,3-Bis[(2-methoxyethoxy)methoxy]-1,3-diphenylacetone – A New Chiral Ketone withC2 Symmetry. Chem Ber 1989, 122, 1215. <http://dx.doi.org/10.1002/cber.19891220632>
• Göndös György, Gera Lajos, Bartók Mihály, Orr James C.: Homogeneous and heterogeneous catalytic asymmetric reactions. J Organomet Chem 1989, 373, 365. <http://dx.doi.org/10.1016/0022-328X(89)85065-X>
• Brunner Henri: Enantioselective catalysis with transition metal complexes. J Organomet Chem 1986, 300, 39. <http://dx.doi.org/10.1016/0022-328X(86)84055-4>
• Karim A., Mortreux A., Petit F., Buono G., Peiffer G., Siv C.: Synthese d'aminophosphinephosphinites chiraux. Utilisation en reduction asymetrique catalytique. J Organomet Chem 1986, 317, 93. <http://dx.doi.org/10.1016/S0022-328X(00)99348-3>
• Oppolzer Wolfgang, Mills Robert J., Reglier Marius: Efficient asymmetric hydrogenations of camphor-soltam-imide-conjugated alkenes. Tetrahetron Lett 1986, 27, 183. <http://dx.doi.org/10.1016/S0040-4039(00)83972-6>
• Schöllkopf Ulrich, Hoppe Inga, Thiele Angelika: Asymmetric synthesis of α-aminophosphonic acids, I enantioselective synthesis of L-(1-aminoethyl)phosphonic acid by asymmetric catalytic hydrogenation ofN-[1-(dimethoxyphosphoryl)ethenyl]formamide. Liebigs Ann Chem 1985, 1985, 555. <http://dx.doi.org/10.1002/jlac.198519850316>
• Brunner Henri, Knott Alfons, Benn Reinhard, Rufińska Anna: Asymmetrische katalysen. J Organomet Chem 1985, 295, 211. <http://dx.doi.org/10.1016/0022-328X(85)80273-4>
• Schurig Volker: Gaschromatographische Enantiomerentrennung an metallkomplexfreien Stationärphasen. Angew Chem 1984, 96, 733. <http://dx.doi.org/10.1002/ange.19840961004>
• Brunner Henri, Reiter Barbara, Riepl Georg: Asymmetrische Katalysen, 14. Enantioselektive Hydrosilylierung prochiraler Ketone mit Rh- und Pt-Komplexen optisch aktiver N-Chelatliganden. Chem Ber 1984, 117, 1330. <http://dx.doi.org/10.1002/cber.19841170407>
• Schöllkopf Ulrich, Scheuer Rainer: Asymmetrische Synthesen über heterocyclische Zwischenstufen, XXIII. Studien zur enantioselektiven Synthese von α-Alkyl-α-(2-furyl)-glycinen durch Alkylieren von an C-6 chiral substituierten 3-(2-Furyl)-3,6-dihydro-2H-1,4-oxazin-2-onen. Liebigs Ann Chem 1984, 1984, 939. <http://dx.doi.org/10.1002/jlac.198419840513>
• Schöllkopf Ulrich, Nozulak Joachim, Groth Ulrich: Asymmetric syntheses via heterocyclic intermediates-XXII. Tetrahedron 1984, 40, 1409. <http://dx.doi.org/10.1016/S0040-4020(01)82426-1>
• Brunner Henri: Rhodium Catalysts for Enantioselective Hydrosilylation—A New Concept in the Development of Asymmetric Catalysts. Angew Chem Int Ed Engl 1983, 22, 897. <http://dx.doi.org/10.1002/anie.198308973>
• Schöllkopf Ulrich, Groth Ulrich, Gull Martin-Reinhold, Nozulak Joachim: Asymmetrische Synthesen über heterocyclische Zwischenstufen, XVIII. Zur enantioselektiven Synthese von (2RS)-Serin-methylestern oder (2R)-Serinen ausgehend vom Bislactimether voncyclo-(-L-Val-Gly-). Liebigs Ann Chem 1983, 1983, 1133. <http://dx.doi.org/10.1002/jlac.198319830706>
• Klabunovskii E. I.: Asymmetric catalysis involving heterocyclic compounds (review). Chem Heterocycl Compd 1983, 19, 233. <http://dx.doi.org/10.1007/BF00513251>
• Olmstead Marilyn M., Guimerans Rosalvina R., Farr James P., Balch Alan L.: Bis(diphenylphosphinomethyl)phenylphosphine as a chelating and bridging ligand. The preparations and molecular structures of palladium complexes. Inorg Chim Ada 1983, 75, 199. <http://dx.doi.org/10.1016/S0020-1693(00)91213-1>
• Schöllkopf Ulrich: Enantioselective synthesis of non-proteinogenic amino acids via metallated bis-lactim ethers of 2,5-diketopiperazines. Tetrahedron 1983, 39, 2085. <http://dx.doi.org/10.1016/S0040-4020(01)91926-X>
• Richter Felix, Vahrenkamp Heinrich: Chirale SFeCoM-Cluster: Enantiomerentrennung und Bestimmung der absoluten Konfiguration. Chem Ber 1982, 115, 3243. <http://dx.doi.org/10.1002/cber.19821151004>
• Hartwig Wolfgang, Schöllkopf Ulrich: Asymmetrische Synthesen über heterocyclische Zwischenstufen, XVI. Enantioselektive Synthese von α-Alkyl-α-phenylglycinen durch Alkylieren von an C-6 chiral substituierten 3,6-Dihydro-3-phenyl-2H-1,4-oxazin-2-onen. Liebigs Ann Chem 1982, 1982, 1952. <http://dx.doi.org/10.1002/jlac.198219821105>
• C. Payne Nicholas, W. Stephan Douglas: Enantiomeric discrimination . J Organomet Chem 1982, 228, 203. <http://dx.doi.org/10.1016/S0022-328X(00)87098-9>
• Brunner Henri, Pieronczyk Willigis, Schönhammer Beate, Streng Karin, Bernal Ivan, Korp Und Jim: Asymmetrische Katalysen, V. Enantioselektive Aminosäuresynthese durch Hydrierung prochiraler Olefine mit Rh-Komplexen des neuen optisch aktiven chelatbildenden Phosphans Norphos. Chem Ber 1981, 114, 1137. <http://dx.doi.org/10.1002/cber.19811140331>
• Schöllkopf Ulrich, Hausberg Hans-Heinrich, Segal Marcos, Reiter Udo, Hoppe Inga, Saenger Wolfram, Lindner Klaus: Asymmetrische Synthesen über heterocyclische Zwischenstufen, IV Asymmetrische Synthese von α-Methylphenylalanin und seinen Analoga durch Alkylieren von 1-chiral substituiertem 4-Methyl-2-imidazolin-5-on. Liebigs Ann Chem 1981, 1981, 439. <http://dx.doi.org/10.1002/jlac.198119810311>
• Schöllkopf Ulrich, Hartwig Wolfgang, Groth Ulrich, Westphalen Karl-Otto: Asymmetrische Synthesen über heterocyclische Zwischenstufen, V Asymmetrische Synthese von α-Methylaminosäuren durch Alkylieren des lithiierten Lactimethers voncyclo-(L-Ala-L-Ala). Liebigs Ann Chem 1981, 1981, 696. <http://dx.doi.org/10.1002/jlac.198119810416>
• Groth Ulrich, Hartwig Wolfgang, Schöllkopf Ulrich: Asymmetrische Synthesen über heterocyclische Zwischenstufen, X. Enantioselektive Synthese von (2R)-2-Methylserinen. Liebigs Ann Chem 1981, 1981, 2407. <http://dx.doi.org/10.1002/jlac.198119811224>
• Johnson Thomas H., Klein Kurt C., Thomen Shirley, Brown Theodore L.: The use of chiral phosphinites in asymmetric chemistry 4. Asymmetric hydrosilylation of ketones effected by rhodium catalysts modified with glucophinite and camphinite. Journal of Molecular Catalysis 1981, 12, 37. <http://dx.doi.org/10.1016/0304-5102(81)80017-X>
• Tsuruya Shigeru, Kuse Tetsushi, Masai Mitsuo, Imamura Sei-Ichiro, Lafont D., Sinou D., Descotes G., Glaser R., Geresh S., De Munck N.A., Verbruggen M.W., Scholten J.J.F.: Oxidative coupling reaction of 2,6-di-alkylphenols catalyzed with copper(II) complexes. Journal of Molecular Catalysis 1981, 10, 285. <http://dx.doi.org/10.1016/0304-5102(81)85051-1>
• Halpern Jack: Mechanistic aspects of homogeneous catalytic hydrogenation and related processes. Inorg Chim Ada 1981, 50, 11. <http://dx.doi.org/10.1016/S0020-1693(00)83716-0>
• Kawai Michio, Masuda Toshio: Asymmetric Reduction of Poly(isopropenyl methyl ketone) via Rhodium(I)-Catalyzed Hydrosilylation. Polym J 1981, 13, 573. <http://dx.doi.org/10.1295/polymj.13.573>
• Glaser Robert, Geresh Shimona, Twaik Menachem: Structural Requirements in Chiral Diphosphine-Rhodium Complexes. XIV. Heptagonal Chelating Ring Flexibility in Rhodium(I) Complexes of Trans -1,2-bis(Diphenylphosphinomethyl)cycloalkanes. Isr. J. Chem. 1980, 20, 102. <http://dx.doi.org/10.1002/ijch.198000058>
• Mazzel M., Marconi W., Riocci M.: Asymmetric hydrogenation of substituted acrylic acids by Rh���-aminophosphine chiral complex supported on mineral clays. Journal of Molecular Catalysis 1980, 9, 381. <http://dx.doi.org/10.1016/0304-5102(80)80030-7>
• Halpern Jack: Homogeneous catalytic hydrogenation: A retrospective account. J Organomet Chem 1980, 200, 133. <http://dx.doi.org/10.1016/S0022-328X(00)88642-8>
• Balavoine G., Brunie S., Kagan H.B.: Structure cristalline du complexe [FeCp((-)DIOP)I] analyse conformationnelle du cycle de chelation de la (-)diop. J Organomet Chem 1980, 187, 125. <http://dx.doi.org/10.1016/S0022-328X(00)90542-4>
• Beck W., Nagel U.: Über ein optisch aktives 1-Phosphino-2-aminopropan aus Ephedrin und die stereospezifische Bildung von Dicarbonylcyclopentadienylmolybdänkomplexen mit diesem Chelatliganden. Z anorg allg Chem 1979, 458, 22. <http://dx.doi.org/10.1002/zaac.19794580103>
• Aviron-Violet P., Colleuille Y., Varagnat J.: Hydrogenation asymetrique en presence de diphosphines chirales. Journal of Molecular Catalysis 1979, 5, 41. <http://dx.doi.org/10.1016/0304-5102(79)80080-2>
• Chan A.S.C., Pluth J.J., Halpern Jack: Intermediates in homogeneous catalytic hydrogenation. The crystal and molecular structure of the methyl(Z)-α-acetamodicinnamate adduct of 1,2-bis(diphenylphosphino)ethanerhodium(I). Inorg Chim Ada 1979, 37, L477. <http://dx.doi.org/10.1016/S0020-1693(00)95478-1>
• ApSimon J.W., Seguin R.P.: Recent advances in asymmetric synthesis. Tetrahedron 1979, 35, 2797. <http://dx.doi.org/10.1016/S0040-4020(01)99497-9>
• Ledor Peter W., Beck Wolfgang, Fick Hans G., Zippel Horst: Metallkomplexe mitN,N-Bis (diphenylphosphino)- α-aminosäureestern. Chem Ber 1978, 111, 615. <http://dx.doi.org/10.1002/cber.19781110221>
• Glaser Robert, Geresh Shimona, Twaik Menachem, Benoiton N.Leo: Structural requirements in chiral diphosphine-rhodium complexes—XII. Tetrahedron 1978, 34, 3617. <http://dx.doi.org/10.1016/0040-4020(78)88439-7>
• Fiorini M., Marcati F., Giongo G.M.: Chiral aminophosphine���rhodium complexes as catalysts for asymmetric hydrogenation of olefins. Journal of Molecular Catalysis 1978, 4, 125. <http://dx.doi.org/10.1016/0304-5102(78)80005-4>
• Sanger Alan R, Tan K.Ghie: Complexes of iridium(I) with the optically active bisphosphine DIOP. Inorg Chim Ada 1978, 31, L439. <http://dx.doi.org/10.1016/S0020-1693(00)94954-5>
• Fiaud J.C., de Gournay A.Hibon, Larcheveque M., Kagan H.B.: Asymmetric catalytic allylation of β-diketones or β-ketoesters with allylic ethers using a palladium-DIOP catalyst: A mechanistic study. J Organomet Chem 1978, 154, 175. <http://dx.doi.org/10.1016/S0022-328X(00)83439-7>
• Winter W., Koppenhöfer B., Schurig V.: Molekülsruktur und abs. konfiguration von (+)-p-menthadien-(1,8)-on-(2)-rhodium(I)-h5-cyclopentadienid, (+)-(4S-Carvon) RhI(C5H5). J Organomet Chem 1978, 150, 145. <http://dx.doi.org/10.1016/S0022-328X(00)85557-6>
• Mestroni G., Zassinovich G., Camus A.: Complexes of rhodium(I) and iridium(I) with 2,2′-bipyridine and similar ligands as hydrogenation catalysts. J Organomet Chem 1977, 140, 63. <http://dx.doi.org/10.1016/S0022-328X(00)84397-1>
• Slack D.A., Baird M.C.: Investigations of olefin hydrogenation catalysts. The major species present in solutions containing rhodium(I) complexes of chelating diphosphines. J Organomet Chem 1977, 142, C69. <http://dx.doi.org/10.1016/S0022-328X(00)88364-3>
• Menzel Hartmut, Beck Wolfgang: Phosphinhaltige terpenderivate als optisch aktive liganden in der homogenen katalyse. J Organomet Chem 1977, 133, 307. <http://dx.doi.org/10.1016/S0022-328X(00)89130-5>
• Zassinovich G., Camus A., Mestroni G.: Complexes of rhodium(I) and iridium(I) with optically active schieff bases. J Organomet Chem 1977, 133, 377. <http://dx.doi.org/10.1016/S0022-328X(00)89137-8>
• Hegedus Louis S.: Transition metal derivatives in organic synthesis . J Organomet Chem 1977, 143, 309. <http://dx.doi.org/10.1016/S0022-328X(00)91964-8>
• Consiglio G.: Asymmetric hydrocarboxylation of olefins . J Organomet Chem 1977, 132, C26. <http://dx.doi.org/10.1016/S0022-328X(00)93732-X>
• Glaser Robert, Twaik Menachem, Geresh Shimona, Blumenfeld Jeanine: Structural requirements in chiral diphosphine-rhodium complexes. VIII. Asymmetric hydrogenation of N-acetyldehydroamino acids with rhodium(I) complexes containing chiral carbocyclic analogues of DIOP. Tetrahetron Lett 1977, 18, 4635. <http://dx.doi.org/10.1016/S0040-4039(01)83588-7>
• Glaser Robert, Blumenfeld Jeanine, Twaik Menachem: Structural requirements in chiral diphosphine-rhodium complexes. X1 asymmetric homogeneous hydrogenation of z-N-acetyldehydroamino acids and esters with (1R,2R)-trans-1,2-bis(diphenylphosphinomethyl)cyclobutane/rhodium(I) complexes. Tetrahetron Lett 1977, 18, 4639. <http://dx.doi.org/10.1016/S0040-4039(01)83589-9>
• Glaser Robert, Geresh Shimona, Blumenfeld Jeanine, Vainas Baruch, Twaik Menachem: Structural Requirements in Chiral Diphosphine-Rhodium Complexes. V. Asymmetric Homogeneous Hydrogenation of Z-α-acetamidocinnamate Esters of Chiral Alcohols with DIOP-Rhodium(I) Complexes and Symmetrical Diphosphine-Rhodium(I) Complexes. Isr. J. Chem. 1976, 15, 17. <http://dx.doi.org/10.1002/ijch.197600005>
• Consiglio Giambattista, Pino Piero: Simultaneous Asymmetric Hydrogenation and Hydroformylation by Chiral Platinum Complexes. Isr. J. Chem. 1976, 15, 221. <http://dx.doi.org/10.1002/ijch.197600040>
• David Garner C., Hughes Barry, King Trevor J., Zassinovich G., Camus A., Mestroni G., Hawkins Clifford J., Peachey Russell M., Szoredi Charles L.: Preparation and characterisation of the cyclodistannoxane [(H2C���CH)4Sn2(O2CCF3)2O]2. Inorganic and Nuclear Chemistry Letters 1976, 12, 859. <http://dx.doi.org/10.1016/0020-1650(76)80137-7>
• Lednor P.W., Beck W., Thiel G.: Reactions of cis-[MCl2(PPh2Cl)2] (M = Pd or Pt), or [PdCl2(PPhCl2)2] with α-amino-acid esters, monosaccharides, thiomonosaccharides, or nucleosides. Inorg Chim Ada 1976, 20, L11. <http://dx.doi.org/10.1016/S0020-1693(00)94060-X>