Pure and Applied Chemistry

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• Pichota Arkadius, Gramlich Volker, Beck Albert K., Seebach Dieter: Preparation and Characterization of New C2- and C1-Symmetric Nitrogen, Oxygen, Phosphorous, and Sulfur Derivatives and Analogs of TADDOL. Part I. HCA 2012, 95, 1239. <http://dx.doi.org/10.1002/hlca.201200146>
• Magrez Magaly, Wencel-Delord Joanna, Alexakis Alexandre, Crévisy Christophe, Mauduit Marc: Significant Asymmetric Amplification in Enantioselective Cu/DiPPAM-catalyzed 1,6- and 1,4-Conjugate Additions of Diethylzinc to (Di)enones. Org. Lett. 2012, 14, 3576. <http://dx.doi.org/10.1021/ol300866p>
• van Koten Gerard: Organocopper Compounds: From Elusive to Isolable Species, from Early Supramolecular Chemistry with RCuI Building Blocks to Mononuclear R2–nCuII and R3–mCuIII Compounds. A Personal View. Organometallics 2012, 31, 7634. <http://dx.doi.org/10.1021/om300830n>
• VAN KOTEN G.: ChemInform Abstract: Asymmetric Catalysis with Chiral Organocopper-Copper Arenethiolates. ChemInform 2010, 25, no. <http://dx.doi.org/10.1002/chin.199441290>
• Janssen Maurits D., Grove David M., van Koten Gerard, Spek Anthony L.: Palladium arenethiolates with intramolecularly coordinating nitrogen lewis bases. Recl Trav Chim Pays-Bas 2010, 115, 286. <http://dx.doi.org/10.1002/recl.19961150505>
• Satyanarayana Tummanapalli, Abraham Susan, Kagan Henri B.: Nichtlineare Effekte in der asymmetrischen Katalyse. Angew Chem 2009, 121, 464. <http://dx.doi.org/10.1002/ange.200705241>
• Satyanarayana Tummanapalli, Abraham Susan, Kagan Henri B.: Nonlinear Effects in Asymmetric Catalysis. Angew Chem Int Ed 2009, 48, 456. <http://dx.doi.org/10.1002/anie.200705241>
• Cotton Hanna K., Norinder Jakob, Bäckvall Jan-E.: Screening of ligands in the asymmetric metallocenethiolatocopper(I)-catalyzed allylic substitution with Grignard reagents. Tetrahedron 2006, 62, 5632. <http://dx.doi.org/10.1016/j.tet.2006.03.100>
• Shi Min, Zhang Wen: Asymmetric 1,4-Addition of Diethylzinc to Cyclic Enones Catalyzed by Cu(I)-Chiral Sulfonamide-Thiophosphoramide Ligands and Lithium Salts. Adv Synth Catal 2005, 347, 535. <http://dx.doi.org/10.1002/adsc.200404321>
• Blanc Catherine, Agbossou-Niedercorn Francine: Chiral aminophosphine–oxazoline auxiliaries applied to copper-catalysed enantioselective 1,4-additions to enones. Tet Asymm 2004, 15, 757. <http://dx.doi.org/10.1016/j.tetasy.2004.01.002>
• Arink Anne M., Braam Thijs W., Keeris Roy, Jastrzebski Johann T. B. H., Benhaim Cyril, Rosset Stéphane, Alexakis Alexandre, van Koten Gerard: Copper(I) Thiolate Catalysts in Asymmetric Conjugate Addition Reactions. Org Lett 2004, 6, 1959. <http://dx.doi.org/10.1021/ol049457u>
• Leschke M., Lang H., Melter M., Rheinwald G., Weber C., Mayer H. A., Pritzkow H., Zsolnai L., Driess A., Huttner G.: Einkernige und zweikernige Kupfer(I)-Komplexe vom Typ LCuCl, LCu2Cl2 und LCu2ClX [L = P(C6H4CH2NMe2-2)3; X = Br, I]. Z anorg allg Chem 2002, 628, 349. <http://dx.doi.org/10.1002/1521-3749(200202)628:2<349::AID-ZAAC349>3.0.CO;2-R>
• Tromp Moniek, van Bokhoven Jeroen A., Arink Anne M., Bitter Johannes H., van Koten Gerard, Koningsberger Diederik C.: Cu K-Edge EXAFS Characterisation of Copper(I) Arenethiolate Complexes in both the Solid and Liquid State: Detection of CuCu Coordination. Chem Eur J 2002, 8, 5667. <http://dx.doi.org/10.1002/1521-3765(20021216)8:24<5667::AID-CHEM5667>3.0.CO;2-O>
• Hupe Eike, Knochel Paul: Formale enantioselektive Michael-Addition mit Umpolung der Reaktivität. Angew Chem 2001, 113, 3109. <http://dx.doi.org/10.1002/1521-3757(20010817)113:16<3109::AID-ANGE3109>3.0.CO;2-N>
• Hupe Eike, Knochel Paul: Formal Enantioselective Michael Addition with Umpolung of Reactivity. Angew Chem Int Ed 2001, 40, 3022. <http://dx.doi.org/10.1002/1521-3773(20010817)40:16<3022::AID-ANIE3022>3.0.CO;2-W>
• Noyori Ryoji, Suga Seiji, Oka Hiromasa, Kitamura Masato: Self and nonself recognition of chiral catalysts: The origin of nonlinear effects in the amino-alcohol catalyzed asymmetric addition of diorganozincs to aldehydes. Chem Record 2001, 1, 85. <http://dx.doi.org/10.1002/tcr.1>
• Lang Heinrich, Leschke Marion, Mayer Hermann A, Melter Michael, Weber Christian, Rheinwald Gerd, Walter Olaf, Huttner Gottfried: A new type of dicopper structure with side arm coordinating triarylphosphane ligands. Inorg Chim Ada 2001, 324, 266. <http://dx.doi.org/10.1016/S0020-1693(01)00619-3>
• Mikami Koichi, Terada Masahiro, Korenaga Toshinobu, Matsumoto Yousuke, Ueki Makoto, Angelaud Rémy: Asymmetrische Aktivierung. Angew Chem 2000, 112, 3676. <http://dx.doi.org/10.1002/1521-3757(20001016)112:20<3676::AID-ANGE3676>3.0.CO;2-W>
• Nakamura Eiichi, Mori Seiji: Warum denn Kupfer? – Strukturen und Reaktionsmechanismen von Organocupratclustern in der Organischen Chemie. Angew Chem 2000, 112, 3902. <http://dx.doi.org/10.1002/1521-3757(20001103)112:21<3902::AID-ANGE3902>3.0.CO;2-L>
• Mikami Koichi, Terada Masahiro, Korenaga Toshinobu, Matsumoto Yousuke, Ueki Makoto, Angelaud Rémy: Asymmetric Activation. Angew Chem 2000, 39, 3532. <http://dx.doi.org/10.1002/1521-3773(20001016)39:20<3532::AID-ANIE3532>3.0.CO;2-L>
• Nakamura Eiichi, Mori Seiji: Wherefore Art Thou Copper? Structures and Reaction Mechanisms of Organocuprate Clusters in Organic Chemistry. Angew Chem 2000, 39, 3750. <http://dx.doi.org/10.1002/1521-3773(20001103)39:21<3750::AID-ANIE3750>3.0.CO;2-L>
• Pichota Arkadius, Pregosin Paul S., Valentini Massimiliano, Wörle Michael, Seebach Dieter: Röntgenstrukturanalyse, Diffusionsmessungen und NOESY-NMR-Untersuchungen chiraler, vierkerniger CuI-Katalysatoren aus einzähnigen Thiol-Derivaten von TADDOL. Angew Chem 2000, 112, 157. <http://dx.doi.org/10.1002/(SICI)1521-3757(20000103)112:1<157::AID-ANGE157>3.0.CO;2-R>
• Bayón J.Carles, Claver Carmen, Masdeu-Bultó Anna M.: Homogeneous catalysis with transition metal complexes containing sulfur ligands. Coord Chem Rev - 1999, 193-195, 73. <http://dx.doi.org/10.1016/S0010-8545(99)00169-1>
• Krause Norbert: Kupferkatalysierte enantioselektive Michael-Additionen: jüngste Fortschritte mit neuen Phosphorliganden. Angew Chem 1998, 110, 295. <http://dx.doi.org/10.1002/(SICI)1521-3757(19980202)110:3<295::AID-ANGE295>3.0.CO;2-B>
• Girard Christian, Kagan Henri B.: Nichtlineare Effekte bei asymmetrischen Synthesen und stereoselektiven Reaktionen. Angew Chem 1998, 110, 3088. <http://dx.doi.org/10.1002/(SICI)1521-3757(19981102)110:21<3088::AID-ANGE3088>3.0.CO;2-A>
• Steenwinkel Pablo, Gossage Robert A., van Koten Gerard: Recent Findings in Cyclometallation of meta-Substituted Aryl Ligands by Platinum Group Metal Complexes by Caryl-R Bond Activation (R=H, CR3, SiR3). Chem Eur J 1998, 4, 759. <http://dx.doi.org/10.1002/(SICI)1521-3765(19980515)4:5<759::AID-CHEM759>3.0.CO;2-K>
• Donkervoort Johannes G., Vicario José L., Rijnberg Evelien, Jastrzebski Johann T.B.H., Kooijman Huub, Spek Anthony L., van Koten Gerard: Formation of mixed aryl–, alkyl–lithium aggregates in the heteroatom assisted lithiation of α,α′-dialkyl substituted 1,3-bis[(dimethylamino)methyl]benzene. J Organomet Chem 1998, 550, 463. <http://dx.doi.org/10.1016/S0022-328X(97)00554-8>
• Krause Norbert, Gerold Andreas: Regio- und stereoselektive Synthesen mit Organokupferreagentien. Angew Chem 1997, 109, 194. <http://dx.doi.org/10.1002/ange.19971090304>
• Gerold Andreas, Jastrzebski Johann T. B. H., Kronenburg Claudia M. P., Krause Norbert, Van Koten Gerard: Bestimmung des Aggregationsgrades von Organokupfer-Verbindungen durch Kryoskopie in Tetrahydrofuran. Angew Chem 1997, 109, 778. <http://dx.doi.org/10.1002/ange.19971090720>
• Steinhagen Henning, Helmchen Günter: Asymmetrische Zweizentren-Katalyse – von der Natur lernen. Angew Chem 1996, 108, 2489. <http://dx.doi.org/10.1002/ange.19961082005>
• Wipf Peter, Venkatraman Srikanth: An improved protocol for azole synthesis with PEG-supported Burgess reagent. Tetrahetron Lett 1996, 37, 4659. <http://dx.doi.org/10.1016/0040-4039(96)00918-5>
• Persson Eva S. M., van Klaveren Mayra, Grove David M., Bäckvall Jan E., van Koten Gerard: ortho-Chelating Arenethiolatocopper(I) Complexes as Versatile Catalysts in the Regioselective Cross-Coupling of Allylic Derivatives withnBuMgI—An Example of Reversed Reactivity of Leaving Groups. Chem Eur J 1995, 1, 351. <http://dx.doi.org/10.1002/chem.19950010605>
• Wipf Peter, Miller Chris P., Venkatraman Srikanth, Fritch Paul C.: Thiolysis of oxazolines: A new, selective method for the direct conversion of peptide oxazolines into thiazolines. Tetrahetron Lett 1995, 36, 6395. <http://dx.doi.org/10.1016/0040-4039(95)01322-9>