Pure and Applied Chemistry

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• Chen I-Hon, Kou Kevin G. M., Le Diane N., Rathbun Colin M., Dong Vy M.: Recognition and Site-Selective Transformation of Monosaccharides by Using Copper(II) Catalysis. Chem. Eur. J. 2014, n/a. <http://dx.doi.org/10.1002/chem.201400133>
• Das Sayantani, Goswami Anandarup, Murali Nagarajan, Asefa Tewodros: Efficient Tertiary Amine/Weak Acid Bifunctional Mesoporous Silica Catalysts for Michael Addition Reactions. ChemCatChem 2013, 5, 910. <http://dx.doi.org/10.1002/cctc.201200551>
• Le Maux Paul, Dorcet Vincent, Simonneaux Gérard: Asymmetric copper-catalyzed Diels–Alder reaction revisited: control of the structure of bis(oxazoline) ligands. Tetrahedron 2013, 69, 8291. <http://dx.doi.org/10.1016/j.tet.2013.06.093>
• Nakata Kenya, Gotoh Kouya, Ono Keisuke, Futami Kengo, Shiina Isamu: Kinetic Resolution of Racemic 2-Hydroxy-γ-butyrolactones by Asymmetric Esterification Using Diphenylacetic Acid with Pivalic Anhydride and a Chiral Acyl-Transfer Catalyst. Org. Lett. 2013, 15, 1170. <http://dx.doi.org/10.1021/ol303453j>
• Huynh Phuong N. H., Walvoord Ryan R., Kozlowski Marisa C.: Rapid Quantification of the Activating Effects of Hydrogen-Bonding Catalysts with a Colorimetric Sensor. J. Am. Chem. Soc. 2012, 134, 15621. <http://dx.doi.org/10.1021/ja3050663>
• Singh Pradeep K., Singh Vinod K.: Chiral 2,6-bis(5',5'-diphenyloxazoline)pyridine as an efficient ligand for asymmetric catalysis. Pure Appl. Chem. 2012, 1. <http://dx.doi.org/10.1351/PAC-CON-11-10-16>
• Hobuß Dennis, Baro Angelika, Axenov Kirill V., Laschat Sabine, Frey Wolfgang: P-Stereogenic Pinene-Derived Phosphoramidites and Their Use in Copper-Catalyzed Conjugate Additions. Eur J Inorg Chem 2011, 2011, 384. <http://dx.doi.org/10.1002/ejic.201000946>
• Li Dong, Ohmiya Hirohisa, Sawamura Masaya: Copper-Catalyzed γ-Selective and Stereospecific Allylic Alkylation of Ketene Silyl Acetals. J Am Chem Soc 2011, 133, 5672. <http://dx.doi.org/10.1021/ja111645q>
• Bigot Aurélien, Williamson Alice E., Gaunt Matthew J.: Enantioselective α-Arylation of N-Acyloxazolidinones with Copper(II)-bisoxazoline Catalysts and Diaryliodonium Salts. J Ann Chem Soc 2011, 133, 13778. <http://dx.doi.org/10.1021/ja206047h>
• Kurono Nobuhito, Ohtsuga Kentaro, Wakabayashi Masanori, Kondo Tadahiro, Ooka Hirohito, Ohkuma Takeshi: Kinetic Resolution of Racemic α-tert-Alkyl-α-hydroxy Esters by Enantiomer-Selective Carbamoylation. J Org Chern 2011, 76, 10312. <http://dx.doi.org/10.1021/jo201940w>
• Eshghi Hossein, Zohuri Gholam Hossein, Damavandi Saman: One-pot multicomponent route to propargylamines using ferric hydrogensulfate. Eur J Chem 2011, 2, 100. <http://dx.doi.org/10.5155/eurjchem.2.1.100-103.175>
• Evans David A., Rovis Tomislav, Johnson Jeffrey S.: ChemInform Abstract: Chiral Copper(II) Complexes as Lewis Acids for Catalyzed Cycloaddition, Carbonyl Addition, and Conjugate Addition Reactions. ChemInform 2010, 31, no. <http://dx.doi.org/10.1002/chin.200031287>
• Singh Pradeep K., Singh Vinod K.: Enantioselective reactions catalyzed by chiral pyridine 2,6-bis(5',5'-diphenyloxazoline)-metal complexes. Pure and App Chemis 2010, 1. <http://dx.doi.org/10.1351/PAC-CON-09-09-40>
• Ma Sandy, Han Xiaoqing, Krishnan Shyam, Virgil Scott C., Stoltz Brian M.: Catalytic Enantioselective Stereoablative Alkylation of 3-Halooxindoles: Facile Access to Oxindoles with C3 All-Carbon Quaternary Stereocenters. Angew Chem 2009, 121, 8181. <http://dx.doi.org/10.1002/ange.200902943>
• Ma Sandy, Han Xiaoqing, Krishnan Shyam, Virgil Scott C., Stoltz Brian M.: Catalytic Enantioselective Stereoablative Alkylation of 3-Halooxindoles: Facile Access to Oxindoles with C3 All-Carbon Quaternary Stereocenters. Angew Chem Int Ed 2009, 48, 8037. <http://dx.doi.org/10.1002/anie.200902943>
• Desimoni Giovanni, Faita Giuseppe, Toscanini Marco, Boiocchi Massimo: A New Copper^II/Isopropylidene-2,2-bis(oxazoline) Catalyst and Its Stable Reactive Complex with Acryloyloxazolidinone in Enantioselective Reactions. Chem Eur J 2009, 15, 9674. <http://dx.doi.org/10.1002/chem.200900908>
• Shizuka Manami, Snapper Marc L.: Catalytic Enantioselective Hosomi-Sakurai Conjugate Allylation of Cyclic Unsaturated Ketoesters. Angew Chem 2008, 120, 5127. <http://dx.doi.org/10.1002/ange.200800628>
• Shizuka Manami, Snapper Marc L.: Catalytic Enantioselective Hosomi-Sakurai Conjugate Allylation of Cyclic Unsaturated Ketoesters. Angew Chem Int Ed 2008, 47, 5049. <http://dx.doi.org/10.1002/anie.200800628>
• Kurono Nobuhito, Kondo Tadahiro, Wakabayashi Masanori, Ooka Hirohito, Inoue Tsutomu, Tachikawa Hiroto, Ohkuma Takeshi: Enantiomer-Selective Carbamoylation of Racemic α-Hydroxy γ-Lactones with Chiral Cu^II Catalysts: An Example of a Highly Active Lewis Acid Catalyzed Reaction. Chem Asian J 2008, 3, 1289. <http://dx.doi.org/10.1002/asia.200700420>
• Schätz Alexander, Rasappan Ramesh, Hager Markus, Gissibl Anja, Reiser Oliver: Dependence of Enantioselectivity on the Ligand/Metal Ratio in the Asymmetric Michael Addition of Indole to Benzylidene Malonates: Electronic Influence of Substrates. Chem Eur J 2008, 14, 7259. <http://dx.doi.org/10.1002/chem.200800508>
• Yu Youqing, Shen Wei, Zhang Jinsheng, He Rongxing, Li Ming: Theoretical investigation of direct amination of β-ketoesters catalyzed by copper(II)-bisoxazoline(BOX). J Mol Model 2008, 14, 237. <http://dx.doi.org/10.1007/s00894-007-0266-8>
• Rasappan Ramesh, Laventine Dominic, Reiser Oliver: Metal-bis(oxazoline) complexes: From coordination chemistry to asymmetric catalysis. Coord Chem Rev - 2008, 252, 702. <http://dx.doi.org/10.1016/j.ccr.2007.11.007>
• Ju Ya-Dong, Xu Li-Wen, Li Li, Lai Guo-Qiao, Qiu Hua-Yu, Jiang Jian-Xiong, Lu Yixin: Noyori’s Ts-DPEN ligand: an efficient bifunctional primary amine-based organocatalyst in enantio- and diastereoselective Michael addition of 1,3-dicarbonyl indane compounds to nitroolefins. Tetrahetron Lett 2008, 49, 6773. <http://dx.doi.org/10.1016/j.tetlet.2008.09.025>
• Doherty Simon, Goodrich Peter, Hardacre Christopher, Knight Julian G., Nguyen Mimi T., Pârvulescu Vasile I., Paun Cristina: Recyclable Copper Catalysts Based on Imidazolium-Tagged Bis(oxazolines): A Marked Enhancement in Rate and Enantioselectivity for Diels–Alder Reactions in Ionic Liquid. Adv Synth Catal 2007, 349, 951. <http://dx.doi.org/10.1002/adsc.200600531>
• Sala Xavier, Santana Naiara, Serrano Isabel, Plantalech Elena, Romero Isabel, Rodríguez Montserrat, Llobet Antoni, Jansat Susanna, Gómez Montserrat, Fontrodona Xavier: The Spectroscopic, Electrochemical and Structural Characterization of a Family of Ru Complexes Containing theC2-Symmetric Didentate Chiral 1,3-Oxazoline Ligand and Their Catalytic Activity. Eur J Inorg Chem 2007, 2007, 5207. <http://dx.doi.org/10.1002/ejic.200700368>
• Orlandi Simonetta, Benaglia Maurizio, Dell’Anna Gianmaria, Celentano Giuseppe: Synthesis of new C1-symmetric bis(oxazoline) ligands with a chelating sidearm for stereoselective Mukaiyama aldol condensations. J Organomet Chem 2007, 692, 2120. <http://dx.doi.org/10.1016/j.jorganchem.2007.02.009>
• Almodovar Iriux, Hövelmann Claas H., Streuff Jan, Nieger Martin, Muñiz Kilian: Enantioselective Diamination of Alkenes by Use of a Bisimidoosmium Reagent with the Aid of Chiral Catalysts. Eur J Org Chem 2006, 2006, 704. <http://dx.doi.org/10.1002/ejoc.200500641>
• Carmona Daniel, Ferrer Joaquina, Lorenzo Mónica, Lahoz Fernando J., Dobrinovitch Isabel T., Oro Luis A.: Synthesis and Characterisation of New Iridium Complexes with the (4S)-2-[2-(Diphenylphosphanyl)phenyl]-4-isopropyl-1,3-oxazoline Ligand That Catalyse Asymmetric Michael Reactions. Eur J Inorg Chem 2005, 2005, 1657. <http://dx.doi.org/10.1002/ejic.200400929>
• Bayardon Jerome, Sinou Denis, Guala Matilde, Desimoni Giovanni: Applications of enantiopure 4,5-diphenyl substituted box and pybox ligands in asymmetric catalysis. Tet Asymm 2004, 15, 3195. <http://dx.doi.org/10.1016/j.tetasy.2004.08.030>
• Kim Sung-Gon, Seong Hye Ran, Kim Jeongryul, Ahn Kyo Han: Synthesis of C1-symmetric chiral tripodal oxazolines through an oxazoline exchange reaction with amino alcohols. Tetrahetron Lett 2004, 45, 6835. <http://dx.doi.org/10.1016/j.tetlet.2004.07.107>
• Matsumura Yoshihiro, Maki Toshihide, Tsurumaki Kazuya, Onomura Osamu: Kinetic resolution of d,l-myo-inositol derivatives catalyzed by chiral Cu(II) complex. Tetrahetron Lett 2004, 45, 9131. <http://dx.doi.org/10.1016/j.tetlet.2004.10.019>
• Andreana Peter R., Liu Chang C., Schreiber Stuart L.: Stereochemical Control of the Passerini Reaction. Org Lett 2004, 6, 4231. <http://dx.doi.org/10.1021/ol0482893>
• Wei C., Mague J. T., Li C.-J.: Asymmetric Catalysis Special Feature Part II: Cu(I)-catalyzed direct addition and asymmetric addition of terminal alkynes to imines. Proceedings of the National Academy of Sciences 2004, 101, 5749. <http://dx.doi.org/10.1073/pnas.0307150101>
• Wroblewski A.E, Bansal V, Kisanga P, Verkade J.G: P(i-PrNCH2CH2)3N: An efficient nonionic catalyst for the regioselective Michael addition of a β,γ-unsaturated ester and a nitrile. Tetrahedron 2003, 59, 561. <http://dx.doi.org/10.1016/S0040-4020(02)01515-6>
• Helmboldt Hannes, Hiersemann Martin: Synthesis and Lewis acid catalyzed Claisen rearrangement of 2-(1,3-oxazolin-2-yl)-substituted allyl vinyl ethers. Tetrahedron 2003, 59, 4031. <http://dx.doi.org/10.1016/S0040-4020(03)00590-8>
• Bolm Carsten, Martin Marc, Simic Oliver, Verrucci Marinella: C₂-Symmetric Bissulfoximines as Ligands in Copper-Catalyzed Enantioselective Diels−Alder Reactions. Org Lett 2003, 5, 427. <http://dx.doi.org/10.1021/ol027273e>
• Hiersemann Martin, Abraham Lars: Catalysis of the Claisen Rearrangement of Aliphatic Allyl Vinyl Ethers. Eur J Org Chem 2002, 2002, 1461. <http://dx.doi.org/10.1002/1099-0690(200205)2002:9<1461::AID-EJOC1461>3.0.CO;2-1>
• Evans David A., Masse Craig E., Wu Jimmy: C₂-Symmetric Sc(III)-Complexes as Chiral Lewis Acids. Catalytic Enantioselective Aldol Additions to Glyoxylate Esters. Org Lett 2002, 4, 3375. <http://dx.doi.org/10.1021/ol026488l>
• Evans David A., Janey Jacob M., Magomedov Nabi, Tedrow Jason S.: Chiral Salen-Aluminum Complexes as Catalysts for Enantioselective Aldol Reactions of Aldehydes and 5-Alkoxyoxazoles: An Efficient Approach to the Asymmetric Synthesis ofsyn andantiβ-Hydroxy-α-amino Acid Derivatives. Angew Chem 2001, 113, 1936. <http://dx.doi.org/10.1002/1521-3757(20010518)113:10<1936::AID-ANGE1936>3.0.CO;2-3>
• Abraham Lars, Czerwonka Regina, Hiersemann Martin: Die katalytische enantioselektive Claisen-Umlagerung eines Allylvinylethers. Angew Chem 2001, 113, 4835. <http://dx.doi.org/10.1002/1521-3757(20011217)113:24<4835::AID-ANGE4835>3.0.CO;2-D>
• Evans David A., Janey Jacob M., Magomedov Nabi, Tedrow Jason S.: Chiral Salen-Aluminum Complexes as Catalysts for Enantioselective Aldol Reactions of Aldehydes and 5-Alkoxyoxazoles: An Efficient Approach to the Asymmetric Synthesis ofsyn andantiβ-Hydroxy-α-amino Acid Derivatives. Angew Chem Int Ed 2001, 40, 1884. <http://dx.doi.org/10.1002/1521-3773(20010518)40:10<1884::AID-ANIE1884>3.0.CO;2-9>
• Abraham Lars, Czerwonka Regina, Hiersemann Martin: The Catalytic Enantioselective Claisen Rearrangement of an Allyl Vinyl Ether. Angew Chem Int E 2001, 40, 4700. <http://dx.doi.org/10.1002/1521-3773(20011217)40:24<4700::AID-ANIE4700>3.0.CO;2-6>
• Rowlands Gareth J.: Ambifunctional cooperative catalysts. Tetrahedron 2001, 57, 1865. <http://dx.doi.org/10.1016/S0040-4020(01)00057-6>
• Hiersemann Martin, Abraham Lars: The Cu(OTf)₂- and Yb(OTf)₃-Catalyzed Claisen Rearrangement of 2-Alkoxycarbonyl-Substituted Allyl Vinyl Ethers. Org Lett 2001, 3, 49. <http://dx.doi.org/10.1021/ol006760w>
• Evans David A., Janey Jacob M.: C₂-Symmetric Cu(II) Complexes as Chiral Lewis Acids. Catalytic, Enantioselective Cycloadditions of Silyl Ketenes. Org Lett 2001, 3, 2125. <http://dx.doi.org/10.1021/ol016096z>
• Dangel Brian D., Polt Robin: Catalysis by Amino Acid-Derived Tetracoordinate Complexes:  Enantioselective Addition of Dialkylzincs to Aliphatic and Aromatic Aldehydes. Org Lett 2000, 2, 3003. <http://dx.doi.org/10.1021/ol0063151>