Pure and Applied Chemistry

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• Marques Carolina S., Burke Anthony J.: Enantioselective catalytic synthesis of ethyl mandelate derivatives using Rh(I)–NHC catalysts and organoboron reagents. Tetrahedron: Asymmetry 2013, 24, 628. <http://dx.doi.org/10.1016/j.tetasy.2013.04.011>
• Gore Rohitkumar G., Truong Thi-Kim-Thu, Pour Milan, Myles Lauren, Connon Stephen J., Gathergood Nicholas: Tandem ionic liquid antimicrobial toxicity and asymmetric catalysis study: carbonyl-ene reactions with trifluoropyruvate. Green Chem. 2013, 15, 2727. <http://dx.doi.org/10.1039/c3gc40875b>
• Doherty Simon, Knight Julian G., Mehdi-Zodeh Hamid: Asymmetric carbonyl-ene and Friedel–Crafts reactions catalysed by Lewis acid platinum group metal complexes of the enantiopure atropisomeric biaryl-like diphosphine (S)-Me2-CATPHOS: a comparison with BINAP. Tet Asymm 2012. <http://dx.doi.org/10.1016/j.tetasy.2012.01.022>
• Zheng Ke, Yin Chengkai, Liu Xiaohua, Lin Lili, Feng Xiaoming: Catalytic Asymmetric Addition of Alkyl Enol Ethers to 1,2-Dicarbonyl Compounds: Highly Enantioselective Synthesis of Substituted 3-Alkyl-3-Hydroxyoxindoles. Angew Chem 2011, 123, 2621. <http://dx.doi.org/10.1002/ange.201007145>
• Zheng Ke, Yin Chengkai, Liu Xiaohua, Lin Lili, Feng Xiaoming: Catalytic Asymmetric Addition of Alkyl Enol Ethers to 1,2-Dicarbonyl Compounds: Highly Enantioselective Synthesis of Substituted 3-Alkyl-3-Hydroxyoxindoles. Angew Chem Int Ed 2011, 50, 2573. <http://dx.doi.org/10.1002/anie.201007145>
• Li Hao, Loh Teck-Peng: A Facile Synthesis of Highly Substituted Five-Membered Rings: Mukaiyama-Aldol-Oxonoium-Ene (MAOE) Domino Reaction. Chem —Asian J 2011, 6, 1948. <http://dx.doi.org/10.1002/asia.201000884>
• Luo He-Kuan, Woo Yuan-Ling, Schumann Herbert, Jacob Chacko, van Meurs Martin, Yang Hai-Yan, Tan Yen-Ting: Palladium(II) Complexes of C2-Bridged Chiral Diphosphines: Application to Enantioselective Carbonyl-Ene Reactions. Adv Synth Catal 2010, 352, 1356. <http://dx.doi.org/10.1002/adsc.200900888>
• Tan Boon Hong, Zhu Ming Kui, Tjan Teguh Budiono W., Loh Teck Peng, Zhao Jun Feng: Enantioselective Carbonyl-Ene Reactions of Trifluoropyruvate in Ionic Liquid via a Recyclable Indium(III)-Pybox Complex. Adv Synth Catal 2010, 352, 2085. <http://dx.doi.org/10.1002/adsc.201000170>
• Liang Yufan, Wang Lin, Zhu Rong, Deng Lujiang, Yang Yunfang, Quan Junmin, Chen Jiahua, Yang Zhen: An Unprecedented Silver Salt Effect Switches the Facial Selectivity in the Vinylogous Mukaiyama Aldol Reaction. Adv Synth Catal 2010, 352, 2387. <http://dx.doi.org/10.1002/adsc.201000420>
• MIKAMI K.: ChemInform Abstract: Asymmetric Catalysis of Carbonyl-Ene Reactions and Related Carbon- Carbon Bond Forming Reactions. ChemInform 2010, 27, no. <http://dx.doi.org/10.1002/chin.199643271>
• Zhao Jun-Feng, Tjan Teguh-Budiono W., Loh Teck-Peng: Significant counterion effect of the In(III)–pybox complex in highly enantioselective carbonyl-ene reactions of ethyl glyoxylate. Tetrahetron Lett 2010, 51, 5649. <http://dx.doi.org/10.1016/j.tetlet.2010.06.066>
• Zheng Ke, Liu Xiaohua, Zhao Jiannan, Yang Yang, Lin Lili, Feng Xiaoming: Highly enantioselective aza-ene-type reaction catalyzed by chiral N,N′-dioxide-nickel(ii) complex. Chem Commun 2010, 46, 3771. <http://dx.doi.org/10.1039/b921042c>
• Peruncheralathan Saravanan, Teller Henrik, Schneider Christoph: Titan&hyphen;Binolat&hyphen;katalysierte Aminolyse von meso&hyphen;Aziridinen &ndash; ein hochenantioselektiver und direkter Zugang zu 1,2&hyphen;Diaminen. Angew Chem 2009, 121, 4943. <http://dx.doi.org/10.1002/ange.200901110>
• Peruncheralathan Saravanan, Teller Henrik, Schneider Christoph: Titanium Binolate Catalyzed Aminolysis of meso Aziridines: A Highly Enantioselective and Direct Access to 1,2-Diamines. Angew Chem Int Ed 2009, 48, 4849. <http://dx.doi.org/10.1002/anie.200901110>
• Bajracharya Gan B., Arai Midori A., Koranne Priti S., Suzuki Takeyuki, Takizawa Shinobu, Sasai Hiroaki: Development of Chiral Spiro Ligands for Metal-Catalyzed Asymmetric Reactions. Bull Chem Soc Jpn 2009, 82, 285. <http://dx.doi.org/10.1246/bcsj.82.285>
• Clarke Matthew L., France Marcia B.: The carbonyl ene reaction. Tetrahedron 2008, 64, 9003. <http://dx.doi.org/10.1016/j.tet.2008.06.075>
• Luo He-Kuan, Khim Lim Bee, Schumann Herbert, Lim Christina, Jie Tan Xiang, Yang Hai-Yan: Enantioselective Carbonyl-Ene Reactions of Arylglyoxals with a Chiral Palladium(II)-BINAP Catalyst. Adv Synth Catal 2007, 349, 1781. <http://dx.doi.org/10.1002/adsc.200600361>
• Kwiatkowski Piotr, Kwiatkowski Jacek, Majer Jakub, Jurczak Janusz: Synthesis of chiral 4-substituted 2-hydroxypent-4-enoic acid derivatives via diastereoselective ene reaction promoted by ZnBr2. Tet Asymm 2007, 18, 215. <http://dx.doi.org/10.1016/j.tetasy.2007.01.007>
• Wakita Kazuhiko, Bajracharya Gan B., Arai Midori A., Takizawa Shinobu, Suzuki Takeyuki, Sasai Hiroaki: Enantioselective glyoxylate-ene reaction using a novel spiro bis(isoxazoline) ligand in copper catalysis. Tet Asymm 2007, 18, 372. <http://dx.doi.org/10.1016/j.tetasy.2007.02.004>
• Chaładaj Wojciech, Kwiatkowski Piotr, Majer Jakub, Jurczak Janusz: Enantioselective glyoxylate-ene reactions catalysed by (salen)chromium(III) complexes. Tetrahetron Lett 2007, 48, 2405. <http://dx.doi.org/10.1016/j.tetlet.2007.01.104>
• Luo He-Kuan, Schumann Herbert: An efficient direct activation method transferring diastereopure platinum complex of BIPHEP to highly efficient Lewis acid catalyst for enantioselective carbonyl-ene reaction. Journal of Molecular Catalysis A 2006, 248, 42. <http://dx.doi.org/10.1016/j.molcata.2005.12.006>
• Pandey Manoj K., Bisai Alakesh, Singh Vinod K.: Enantioselective turnover in glyoxylate-ene reactions catalyzed by chiral copper complexes. Tetrahetron Lett 2006, 47, 897. <http://dx.doi.org/10.1016/j.tetlet.2005.11.159>
• Kano Taichi, Konishi Teppei, Konishi Shunsuke, Maruoka Keiji: Design of chiral tin(IV) aryloxide as a mild Lewis acid catalyst for enantioselective Diels–Alder reaction. Tetrahetron Lett 2006, 47, 873. <http://dx.doi.org/10.1016/j.tetlet.2005.12.001>
• Fu Fan, Teo Yong-Chua, Loh Teck-Peng: Catalytic enantioselective Mukaiyama aldol reaction via a chiral indium(III)–pybox complex. Tetrahetron Lett 2006, 47, 4267. <http://dx.doi.org/10.1016/j.tetlet.2006.04.029>
• Chen Dianjun, Guo Li, Kotti S.R.S. Saibabu, Li Guigen: The first asymmetric catalytic halo aldol reaction of β-iodo allenoates with aldehydes by using chiral salen catalyst. Tet Asymm 2005, 16, 1757. <http://dx.doi.org/10.1016/j.tetasy.2005.03.038>
• Maier Peter, Redlich Hartmut, Richter Jessica: High enantio- and diastereoselective induction of BINOL- and TADDOL-modified vinyloxy ethoxides in C–C coupling reactions with aldehydes. Tet Asymm 2005, 16, 3848. <http://dx.doi.org/10.1016/j.tetasy.2005.10.001>
• Mukaiyama Teruaki: Strategien zur Erforschung neuer Reaktionen. Angew Chem 2004, 116, 5708. <http://dx.doi.org/10.1002/ange.200300641>
• Mukaiyama Teruaki: Explorations into New Reaction Chemistry. Angew Chem Int Ed 2004, 43, 5590. <http://dx.doi.org/10.1002/anie.200300641>
• De Rosa Margherita, Acocella Maria Rosaria, Villano Rosaria, Soriente Annunziata, Scettri Arrigo: Ti(IV)/BINOL-catalyzed asymmetric aldol reaction of a masked acetoacetic ester: pronounced influence of catalyst concentration on nonlinear effects. Tetrahetron Lett 2003, 44, 6087. <http://dx.doi.org/10.1016/S0040-4039(03)01470-9>
• Yang Dan, Yang Min, Zhu Nian-Yong: Chiral Lewis Acid-Catalyzed Enantioselective Intramolecular Carbonyl Ene Reactions of Unsaturated α-Keto Esters. Org Lett 2003, 5, 3749. <http://dx.doi.org/10.1021/ol035486d>
• Spino Claude: CHIRAL ENOLATE EQUIVALENTS. A REVIEW. Org Prep Proced Int 2003, 35, 1. <http://dx.doi.org/10.1080/00304940309355794>
• Kezuka Satoko, Kogami Youichi, Ikeno Taketo, Yamada Tohru: Enantioselective Carbonyl-Ene Reaction of Glyoxal Derivatives Catalyzed by Cationic 3-Oxobutylideneaminatocobalt(III) Complexes. Bull Chem Soc Jpn 2003, 76, 49. <http://dx.doi.org/10.1246/bcsj.76.49>
• Moore David, Pu Lin: BINOL-Catalyzed Highly Enantioselective Terminal Alkyne Additions to Aromatic Aldehydes. Org Lett 2002, 4, 1855. <http://dx.doi.org/10.1021/ol025825n>
• Seebach Dieter, Beck Albert K., Heckel Alexander: TADDOLe, ihre Derivate und Analoga – vielseitige chirale Hilfsstoffe. Angew Chem 2001, 113, 96. <http://dx.doi.org/10.1002/1521-3757(20010105)113:1<96::AID-ANGE96>3.0.CO;2-B>
• Seebach Dieter, Beck Albert K., Heckel Alexander: TADDOLs, Their Derivatives, and TADDOL Analogues: Versatile Chiral Auxiliaries. Angewandte Chemie-Int Ed 2001, 40, 92. <http://dx.doi.org/10.1002/1521-3773(20010105)40:1<92::AID-ANIE92>3.0.CO;2-K>
• Aspinall Helen C., Bickley Jamie F., Dwyer Jennifer L. M., Greeves Nicholas, Steiner Alexander: Lithium Binaphtholates: Chiral Chains and Clusters. Angew Chem 2000, 112, 2980. <http://dx.doi.org/10.1002/1521-3757(20000818)112:16<2980::AID-ANGE2980>3.0.CO;2-I>
• Greeves Nicholas, Steiner Alexander, Aspinall Helen C., Bickley Jamie F., Dwyer Jennifer L. M.: Lithium Binaphtholates: Chiral Chains and Clusters. Angew Chem 2000, 39, 2858. <http://dx.doi.org/10.1002/1521-3773(20000818)39:16<2858::AID-ANIE2858>3.0.CO;2-T>
• Heckel Alexander, Seebach Dieter: Verankerung von TADDOL auf porösem Kieselgel mit hoher Beladung und erste Anwendungen in der enantioselektiven Katalyse. Angew Chem 2000, 112, 165. <http://dx.doi.org/10.1002/(SICI)1521-3757(20000103)112:1<165::AID-ANGE165>3.0.CO;2-V>
• Hao Jian, Hatano Manabu, Mikami Koichi: Chiral Palladium(II)-Catalyzed Asymmetric Glyoxylate−Ene Reaction:  Alternative Approach to the Enantioselective Synthesis of α-Hydroxy Esters. Org Lett 2000, 2, 4059. <http://dx.doi.org/10.1021/ol0066983>
• Braddock D. Christopher, Brown John M.: Catalytic and Stoichiometric Lewis Acid Participation in Aldehyde Ene Cyclisations. Collect Czech Chem Commun 2000, 65, 741. <http://dx.doi.org/10.1135/cccc20000741>
• Monti Honoré, Laval Gilles, Féraud Michel: Silicon-Controlled Intramolecular Thermal H-Ene Reaction – A New Access to a Key Intermediate of (±)-cis-γ-Irone. Eur J Org Chem 1999, 1999, 1825. <http://dx.doi.org/10.1002/(SICI)1099-0690(199908)1999:8<1825::AID-EJOC1825>3.0.CO;2-5>
• Kobayashi Ichiro, Hashimoto Shigeharu, Suzuki Yoshiichi, Yajima Tomoko, Kawauchi Susumu, Imase Tatsuya, Terada Masahiro, Mikami Koichi: Effects of Conformation of Diastereomer Liquid Crystals on the Preference of Antiferroelectricity. Molecular Crystals and Liquid Crystals Science and Technology Section A Molecular Crystals and Liquid Crystals 1999, 328, 131. <http://dx.doi.org/10.1080/10587259908026053>
• Catalytic C-H Bond Activation-Asymmetric Olefin Coupling Reaction:The First Example of Asymmetric Fujiwara-Moritani Reaction Catalyzed by Chiral Palladium(II) Complexes. Chem Lett 1999, 55. <http://dx.doi.org/10.1246/cl.1999.55>
• Terada Masahiro, Matsumoto Yousuke, Nakamura Yoshiyuki, Mikami Koichi: The effect of counter cations in zeolites on the efficient preparation of the binaphthol–titanium complex. Journal of Molecular Catalysis A 1998, 132, 165. <http://dx.doi.org/10.1016/S1381-1169(97)00239-2>
• Mikami Koichi, Terada Masahiro, Matsumoto Yousuke, Tanaka Masako, Nakamura Yoshiyuki: Efficient preparation of binaphthol-derived active μ3-oxo titanium catalyst by using hydrated Na-zeolites (molecular sieves). Microp Mesop Mat 1998, 21, 461. <http://dx.doi.org/10.1016/S1387-1811(98)00022-5>
• Nagel Ulrich, Nedden Hans GüNter: Enantioselective Catalysis, XIVAsymmetric Grignard Cross-Coupling Reaction: An Investigation of the Factors Influencing Asymmetric Induction with a New Type of Pyrrolidinephosphane. Chem Ber 1997, 130, 535. <http://dx.doi.org/10.1002/cber.19971300414>
• Nicht-lineare Effekte in der asymmetrischen Synthese. Nachr Chem Tech Lab 1997, 45, 392. <http://dx.doi.org/10.1002/nadc.19970450415>
• Corey E.J., Barnes-Seeman David, Lee Thomas W., Goodman Steven N.: A transition-state model for the mikami enantioselective ene reaction. Tetrahetron Lett 1997, 38, 6513. <http://dx.doi.org/10.1016/S0040-4039(97)01517-7>
• Fu-Yao Zhang, Chan Albert S.C.: Enantioselective addition of diethylzinc to aromatic aldehydes catalyzed by titanium-5,5′,6,6′,7,7′,8,8′-octahydro-1,1′-bi-2-naphthol complex. Tet Asymm 1997, 8, 3651. <http://dx.doi.org/10.1016/S0957-4166(97)00501-6>
• Kobayashi Ichiro, Suzuki Yoshiichi, Yajima Tomoko, Kawauchi Susumu, Terada Masahiro, Mikami Koichi: Diastereomer Effects on Antiferroelectricity and Ferroelectricity of the Newly Synthesized Liquid Crystals. Molecular Crystals and Liquid Crystals Science and Technology Section A Molecular Crystals and Liquid Crystals 1997, 303, 165. <http://dx.doi.org/10.1080/10587259708039421>
• Mikami Koichi, Yoshida Akihiro, Matsumoto Youichi: Catalytic asymmetric carbonyl-ene reactions with alkynylogous and vinylogous glyoxylates: Application to controlled synthesis of chiral isocarbacyclin analogues. Tetrahetron Lett 1996, 37, 8515. <http://dx.doi.org/10.1016/0040-4039(96)01954-5>
• Mikami Koichi, Yajima Tomoko, Terada Masahiro, Kawauchi Susumu, Suzuki Yoshiichi, Kobayashi Ichiro: Diastereotropic Phenomena for the Appearance of SmCA* Phase in .ALPHA.-Trifluoromethyl-.BETA.-methyl-substituted Liquid Crystalline Molecules. Chem Lett 1996, 861. <http://dx.doi.org/10.1246/cl.1996.861>