Pure and Applied Chemistry

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• Kwok Sen Wai, Zhang Li, Grimster Neil P., Fokin Valery V.: Catalytic Asymmetric Transannulation of NH -1,2,3-Triazoles with Olefins. Angew. Chem. 2014, 126, 3520. <http://dx.doi.org/10.1002/ange.201306706>
• Kwok Sen Wai, Zhang Li, Grimster Neil P., Fokin Valery V.: Catalytic Asymmetric Transannulation of NH -1,2,3-Triazoles with Olefins. Angew. Chem. Int. Ed. 2014, 53, 3452. <http://dx.doi.org/10.1002/anie.201306706>
• Tayama Eiji, Horikawa Kouki, Iwamoto Hajime, Hasegawa Eietsu: Copper(II)–acid catalyzed cyclopropanation of 1,3-dienamides by electrophilic activation of α-aryl diazoesters. Tetrahedron Letters 2014. <http://dx.doi.org/10.1016/j.tetlet.2014.03.115>
• Pellissier Hélène, Clavier Hervé: Enantioselective Cobalt-Catalyzed Transformations. Chem. Rev. 2014, 114, 2775. <http://dx.doi.org/10.1021/cr4004055>
• Noyori Ryoji: Fakten sind der Feind der Wahrheit - Betrachtungen über Zufallsentdeckungen und ungeahnte Entwicklungen der asymmetrischen Katalyse. Angew. Chem. 2013, 125, 83. <http://dx.doi.org/10.1002/ange.201205537>
• Noyori Ryoji: Facts are the Enemy of Truth-Reflections on Serendipitous Discovery and Unforeseen Developments in Asymmetric Catalysis. Angew. Chem. Int. Ed. 2013, 52, 79. <http://dx.doi.org/10.1002/anie.201205537>
• Pradeep Chullikkattil P., Das Samar K.: Coordination and supramolecular aspects of the metal complexes of chiral N-salicyl-β-amino alcohol Schiff base ligands: Towards understanding the roles of weak interactions in their catalytic reactions. Coordination Chemistry Reviews 2013, 257, 1699. <http://dx.doi.org/10.1016/j.ccr.2013.01.028>
• Gharaati Shadab, Moghadam Majid, Tangestaninejad Shahram, Mirkhani Valiollah, Mohammadpoor-Baltork Iraj, Barati Behjat, Sadegh Faranak: High-valent tin(IV) porphyrins: Efficient and selective catalysts for cyclopropanation of styrene derivatives with EDA under mild conditions. Journal of Organometallic Chemistry 2013, 741-742, 78. <http://dx.doi.org/10.1016/j.jorganchem.2013.05.046>
• Masterson Douglas S., Shirley Caitlyne, Glatzhofer Daniel T.: N-(4-[2.2]paracyclophanyl)-2′-hydroxyacetophenone imine: An effective paracyclophane Schiff-base ligand for use in catalytic asymmetric cyclopropanation reactions. Journal of Molecular Catalysis A: Chemical 2012, 361-362, 111. <http://dx.doi.org/10.1016/j.molcata.2012.05.009>
• Uddin Ahmad Jahir, Nieger Martin, Sundberg Markku R., Leskelä Markku, Repo Timo: Solid and solution structures of bulky tert-butyl substituted salicylaldimines. J Molec Struct 2011, 995, 9. <http://dx.doi.org/10.1016/j.molstruc.2011.02.033>
• Brunner H., Kluschanzoff H., Wutz K.: Enantioselective Catalysis, 471 Rhodium(II)-Carboxylate Complexes and Their Use In the Enantioselective Cyclopropanation. Bull Soc Chim Belges 2010, 98, 63. <http://dx.doi.org/10.1002/bscb.19890980107>
• Pfaltz Andreas: Enantioselective Catalysis with Metal Complexes Containing Heterocyclic Ligands. Bull Soc Chim Belges 2010, 99, 729. <http://dx.doi.org/10.1002/bscb.19900990910>
• Ghanem Ashraf, Gardiner Michael G., Williamson Rachel M., Müller Paul: First X-ray Structure of a N-Naphthaloyl-Tethered Chiral Dirhodium(II) Complex: Structural Basis for Tether Substitution Improving Asymmetric Control in Olefin Cyclopropanation. Chem Eur J 2010, 16, 3291. <http://dx.doi.org/10.1002/chem.200903231>
• Doyle Michael P.: Chiral catalysts for enantioselective carbenoid cyclopropanation reactions. Recl Trav Chim Pays-Bas 2010, 110, 305. <http://dx.doi.org/10.1002/recl.19911100702>
• Wang Yuan-Shan, Zheng Ren-Chao, Xu Jian-Miao, Liu Zhi-Qiang, Cheng Feng, Feng Zhi-Hua, Liu Li-Ling, Zheng Yu-Guo, Shen Yin-Chu: Enantioselective hydrolysis of (R)-2, 2-dimethylcyclopropane carboxamide by immobilized cells of an R-amidase-producing bacterium, Delftia tsuruhatensis CCTCC M 205114, on an alginate capsule carrier. J Ind Microbiol Biotech 2010, 37, 503. <http://dx.doi.org/10.1007/s10295-010-0696-7>
• Mezzetti Antonio: Ruthenium complexes with chiral tetradentate PNNP ligands: Asymmetric catalysis from the viewpoint of inorganic chemistry. Dalton Trans 2010, 39, 7851. <http://dx.doi.org/10.1039/c0dt00119h>
• Doyle Michael P.: Außergewöhnlich selektive Cyclopropanierungen mit chiralen Cobalt(II)-Porphyrin-Katalysatoren. Angew Chem 2009, 121, 864. <http://dx.doi.org/10.1002/ange.200804940>
• Doyle Michael P.: Exceptional Selectivity in Cyclopropanation Reactions Catalyzed by Chiral Cobalt(II)-Porphyrin Catalysts. Angew Chem Int Ed 2009, 48, 850. <http://dx.doi.org/10.1002/anie.200804940>
• Krief Alain, Jeanmart Stephane, Kremer Adrian: Inspired by flowers: Synthetic routes to scalemic deltamethrinic acid. biorg med chem 2009, 17, 2555. <http://dx.doi.org/10.1016/j.bmc.2009.01.030>
• Kassaee M.Z., Soleimani-Amiri S., Buazar F., Rad H. Aref, Zhang Xu, Geng Zhi-Yuan, Wang Yong-Cheng, Li Wen-Qiang, Wang Zheng, Liu Feng-Xia, Ji Hong-Fang, Shen Liang: Novel disilyleno- and digermylenocarbenes and SiSi containing cyclopropenylidenes at theoretical levels. Journal of Molecular Structure: THEOCHEM 2009, 893, 48. <http://dx.doi.org/10.1016/j.theochem.2008.09.016>
• Krief Alain, Jeanmart Stephane, Kremer Adrian: Reprint of “Inspired by flowers: Synthetic routes to scalemic deltamethrinic acid” [Bioorg. Med. Chem. 17 (2009) 2555–2575]. biorg med chem 2009, 17, 4106. <http://dx.doi.org/10.1016/S0968-0896(09)00513-6>
• Abramovitch Adi, Fensterbank Louis, Malacria Max, Marek Ilan: Convergent Preparation of Enantiomerically Pure Polyalkylated Cyclopropane Derivatives. Angew. Chem. 2008, 120, 6971. <http://dx.doi.org/10.1002/ange.200802093>
• Abramovitch Adi, Fensterbank Louis, Malacria Max, Marek Ilan: Convergent Preparation of Enantiomerically Pure Polyalkylated Cyclopropane Derivatives. Angew Chem Int Ed 2008, 47, 6865. <http://dx.doi.org/10.1002/anie.200802093>
• Pellissier Hélène: Recent developments in asymmetric cyclopropanation. Tetrahedron 2008, 64, 7041. <http://dx.doi.org/10.1016/j.tet.2008.04.079>
• Çolak Mehmet, Demirel Nadir: Enantioselective nitroaldol (Henry) reaction catalyzed by chiral Schiff-base ligands. Tet Asymm 2008, 19, 635. <http://dx.doi.org/10.1016/j.tetasy.2008.02.005>
• Lai Guoyin, Wang Sujing, Wang Zhiyong: Asymmetric Henry reaction catalyzed by a copper tridentate chiral schiff-base complex. Tet Asymm 2008, 19, 1813. <http://dx.doi.org/10.1016/j.tetasy.2008.06.036>
• Adamo Mauro F.A., Konda Vivekananda R.: A multicomponent synthesis of cyclopropanes. Tetrahetron Lett 2008, 49, 6224. <http://dx.doi.org/10.1016/j.tetlet.2008.08.033>
• Fraile José M, García José I., Gissibl Anja, Mayoral José A., Pires Elísabet, Reiser Oliver, Roldán Marta, Villalba Isabel: C1-Symmetric VersusC2-Symmetric Ligands in Enantioselective Copper–Bis(oxazoline)-Catalyzed Cyclopropanation Reactions. Chem Eur J 2007, 13, 8830. <http://dx.doi.org/10.1002/chem.200700681>
• Blaser Hans-Ulrich: Industrial asymmetric catalysis: Approaches and results. Rend Fis Acc Lincei 2007, 18, 281. <http://dx.doi.org/10.1007/BF02934925>
• Zhong Jiangchun, Guo Hongchao, Wang Mingan, Yin Mingming, Wang Min: Asymmetric diethylzinc addition and phenyl transfer to aldehydes using chiral cis-cyclopropane-based amino alcohols. Tet Asymm 2007, 18, 734. <http://dx.doi.org/10.1016/j.tetasy.2007.03.006>
• Çolak Mehmet, Aral Tarık, Hoşgören Halil, Demirel Nadir: Synthesis of novel chiral Schiff-base ligands and their application in asymmetric nitro aldol (Henry) reaction. Tet Asymm 2007, 18, 1129. <http://dx.doi.org/10.1016/j.tetasy.2007.04.025>
• Rosini Goffredo, Ayoub Claudia, Borzatta Valerio, Marotta Emanuela, Mazzanti Andrea, Righi Paolo: The same and not the same. Similarities and differences in the resolution of trans-chrysanthemic acid of industrial origin by the enantiomers of some threo-1-aryl-2-dimethylamino-1,3-propanediols. Green Chem 2007, 9, 441. <http://dx.doi.org/10.1039/b615785h>
• Weathers Thomas M., Doyle Michael P., Carducci Michael D.: Substrateversus Catalyst Control of Stereoselectivity in the Cyclopropanation of a Carbon-Carbon Double Bond Linked to the Reactant Diazoacetate through a Chiral Linker. Adv Synth Catal 2006, 348, 449. <http://dx.doi.org/10.1002/adsc.200505357>
• Muñiz Kilian: Asymmetrische Katalyse mit Metall-Komplexen. Bild oder Spiegelbild?. Chem Unserer Zeit 2006, 40, 112. <http://dx.doi.org/10.1002/ciuz.200600375>
• Jiang Chen, Li Daliang, Wen Jiwu, You Tianpa: QSAR study of the enantiomeric excess in asymmetric catalytic reactions with topological indices and an artificial neural network. J Mol Model 2006, 13, 91. <http://dx.doi.org/10.1007/s00894-006-0126-y>
• Zhang Yanmei, Sun Wei, Freund Christelle, Santos Ana M., Herdtweck Eberhardt, Mink Janos, Kühn Fritz E.: Cationic copper(I) and silver(I) nitrile complexes with fluorinated weakly coordinating anions: Metal–nitrile bond strength and its influence on the catalytic performance. Inorg Chim Ada 2006, 359, 4723. <http://dx.doi.org/10.1016/j.ica.2005.12.044>
• Gan Changsheng, Lai Guoyin, Zhang Zuhui, Wang Zhiyong, Zhou Ming-Ming: Efficient and enantioselective nitroaldol reaction catalyzed by copper Schiff-base complexes. Tet Asymm 2006, 17, 725. <http://dx.doi.org/10.1016/j.tetasy.2006.01.032>
• Ma Moreno Rosa, Rosol Malgorzata, Moyano Albert: Salicylaldehyde Schiff bases derived from 2-ferrocenyl-2-amino alcohols. Part 1: New chiral ligands for the titanium-catalyzed enantioselective cyanation of aldehydes. Tet Asymm 2006, 17, 1089. <http://dx.doi.org/10.1016/j.tetasy.2006.03.016>
• Moreno Rosa Ma, Moyano Albert: Salicylaldehyde Schiff bases derived from 2-ferrocenyl-2-amino alcohols. Part 2: Stereochemical divergence in the titanium-promoted enantioselective diketene addition to benzaldehyde. Tet Asymm 2006, 17, 1104. <http://dx.doi.org/10.1016/j.tetasy.2006.03.017>
• Meng Qingxi, Li Ming: Theoretical insights of copper(I) carbenes. Journal of Molecular Structure: THEOCHEM 2006, 765, 13. <http://dx.doi.org/10.1016/j.theochem.2006.02.026>
• Keliher Edmund J., Burrell Richard C., Chobanian Harry R., Conkrite Karina L., Shukla Rajesh, Baldwin John E.: Efficient syntheses of four stable-isotope labeled (1R)-menthyl (1S,2S)-(+)-2-phenylcyclopropanecarboxylates. Org Biomol Chem 2006, 4, 2777. <http://dx.doi.org/10.1039/b605912k>
• Rosini Goffredo, Ayoub Claudia, Borzatta Valerio, Mazzanti Andrea, Marotta Emanuela, Righi Paolo: p1,n1 Salts: self-assembled supramolecular structures sequestering racemates. Diastereomeric separation and enantiomeric enrichment of trans-chrysanthemic acid. Chem Commun 2006, 4294. <http://dx.doi.org/10.1039/b608405b>
• Rh2(Opiv)4-Catalyzed Reactions of Diazo Compound Derived from Meldrum's Acid and Styrenes. Efficient Synthesis of Cyclopropanes. Bulletin of the Korean Chemical Society 2006, 27, 503. <http://dx.doi.org/10.5012/bkcs.2006.27.4.503>
• Cornejo Alfonso, Fraile José M., García José I., Gil María J., Martínez-Merino Víctor, Mayoral José A., Salvatella Luis: Asymmetric versusC2-Symmetric Ligands: Origin of the Enantioselectivity in Ruthenium-Pybox-Catalyzed Cyclopropanation Reactions. Angew Chem 2005, 117, 462. <http://dx.doi.org/10.1002/ange.200461418>
• Cornejo Alfonso, Fraile José M., García José I., Gil María J., Martínez-Merino Víctor, Mayoral José A., Salvatella Luis: Asymmetric versusC2-Symmetric Ligands: Origin of the Enantioselectivity in Ruthenium-Pybox-Catalyzed Cyclopropanation Reactions. Angew Chem Int Ed 2005, 44, 458. <http://dx.doi.org/10.1002/anie.200461418>
• Ghanem Ashraf, Aboul-Enein Hassan Y., Müller Paul: One-pot synthesis and chiral analysis of cyclopropane derivatives. Chirality 2005, 17, 44. <http://dx.doi.org/10.1002/chir.20093>
• Burtoloso Antonio Carlos B., Correia Carlos Roque D.: Asymmetric synthesis of cis-2,4-disubstituted azetidin-3-ones from metal carbene chemistry. J Organomet Chem 2005, 690, 5636. <http://dx.doi.org/10.1016/j.jorganchem.2005.07.016>
• Wang Lingping, Kong Aiguo, Chen Bo, Ding Hanming, Shan Yongkui, He Mingyuan: Direct synthesis, characterization of Cu-SBA-15 and its high catalytic activity in hydroxylation of phenol by H2O2. Journal of Molecular Catalysis A 2005, 230, 143. <http://dx.doi.org/10.1016/j.molcata.2004.12.027>
• Chaudhari Raghunath V., Mills Patrick L.: Multiphase catalysis and reaction engineering for emerging pharmaceutical processes. Chem Eng Set 2004, 59, 5337. <http://dx.doi.org/10.1016/j.ces.2004.07.105>
• Iglesias Ana L., Aguirre Gerardo, Somanathan Ratnasamy, Parra-Hake Miguel: New chiral Schiff base–Cu(II) complexes as cyclopropanation catalysts. J Polyhedron 2004, 23, 3051. <http://dx.doi.org/10.1016/j.poly.2004.09.007>
• Itagaki Makoto, Hagiya Koji, Kamitamari Masashi, Masumoto Katsuhisa, Suenobu Katsuhiro, Yamamoto Yohsuke: Highly efficient chiral copper Schiff-base catalyst for asymmetric cyclopropanation of 2,5-dimethyl-2,4-hexadiene. Tetrahedron 2004, 60, 7835. <http://dx.doi.org/10.1016/j.tet.2004.06.073>
• Berkessel Albrecht, Kaiser Patrick, Lex Johann: Electronically Tuned Chiral Ruthenium Porphyrins: Extremely Stable and Selective Catalysts for Asymmetric Epoxidation and Cyclopropanation. Chem Eur J 2003, 9, 4746. <http://dx.doi.org/10.1002/chem.200305045>
• Straub Bernd F, Gruber Irene, Rominger Frank, Hofmann Peter: Mechanism of copper(I)-catalyzed cyclopropanation: a DFT study calibrated with copper(I) alkene complexes. J Organomet Chem 2003, 684, 124. <http://dx.doi.org/10.1016/S0022-328X(03)00520-5>
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• Xu Youjun, Ohori Ken, Ohshima Takashi, Shibasaki Masakatsu: A practical large-scale synthesis of enantiomerically pure 3-[bis(methoxycarbonyl)methyl]cyclohexanone via catalytic asymmetric Michael reaction. Tetrahedron 2002, 58, 2585. <http://dx.doi.org/10.1016/S0040-4020(02)00141-2>
• Pigro Maria Cristina, Angiuoni Gabriella, Piancatelli Giovanni: Readily available carbohydrate-derived imines and amides as chiral ligands for asymmetric catalysis. Tetrahedron 2002, 58, 5459. <http://dx.doi.org/10.1016/S0040-4020(02)00510-0>
• Chiral C₂-Symmetric &#x03B1;-and &#x03C9;-Diimines with Bulky Substituents at Nitrogen: Synthesis and Catalytic Properties of Some Copper Complexes. Bulletin of the Korean Chemical Society 2002, 23, 721. <http://dx.doi.org/10.5012/bkcs.2002.23.5.721>
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