Pure and Applied Chemistry

CrossRef Cited-by Linking

• Allgäuer Dominik S., Mayr Herbert: Electrophilicities of 1,2-Disubstituted Ethylenes. Eur. J. Org. Chem. 2014, n/a. <http://dx.doi.org/10.1002/ejoc.201301779>
• Levkov Igor V., Cassel Stephanie, Voitenko Zoia V., Saffon Nathalie, Lattes Armand, Rico-Lattes Isabelle: Synthesis, Autoorganization and Reactivity of Amphiphilic Derivatives of 1-Aminoisoindole in Water and Formamide. J Surfact Deterg 2014, 17, 101. <http://dx.doi.org/10.1007/s11743-013-1476-y>
• Raynal Matthieu, Ballester Pablo, Vidal-Ferran Anton, van Leeuwen Piet W. N. M.: Supramolecular catalysis. Part 1: non-covalent interactions as a tool for building and modifying homogeneous catalysts. Chem. Soc. Rev. 2014, 43, 1660. <http://dx.doi.org/10.1039/c3cs60027k>
• Raynal Matthieu, Ballester Pablo, Vidal-Ferran Anton, van Leeuwen Piet W. N. M.: Supramolecular catalysis. Part 2: artificial enzyme mimics. Chem. Soc. Rev. 2014, 43, 1734. <http://dx.doi.org/10.1039/c3cs60037h>
• Chemouri Hafida, Mekelleche Sidi Mohamed: On the importance of hydrogen bonding in the promotion of Diels–Alder reactions of unactivated aldehydes: a computational study. Molecular Physics 2014, 112, 601. <http://dx.doi.org/10.1080/00268976.2013.846485>
• Shionozaki Nobuhiro, Iwamura Naoki, Tanaka Ryo, Makino Kimiko, Uchiro Hiromi: Total Synthesis of Diaporthichalasin by Using the IntramolecularDiels-Alder Reaction of an α,β-Unsaturated γ-Hydroxylactam in Aqueous Media. Chem. Asian J. 2013, 8, 1243. <http://dx.doi.org/10.1002/asia.201201230>
• Bernardon Claire, Louis Benoît, Bénéteau Valérie, Pale Patrick: Diels-Alder Reaction between Isoprene and Methyl Acrylate over Different Zeolites: Influence of Pore Topology and Acidity. ChemPlusChem 2013, 78, 1134. <http://dx.doi.org/10.1002/cplu.201300157>
• Chia Mei, Haider M. Ali, Pollock Gerald, Kraus George A., Neurock Matthew, Dumesic James A.: Mechanistic Insights into Ring-Opening and Decarboxylation of 2-Pyrones in Liquid Water and Tetrahydrofuran. J. Am. Chem. Soc. 2013, 135, 5699. <http://dx.doi.org/10.1021/ja312075r>
• Verma Akhilesh K., Choudhary Deepak, Saunthwal Rakesh K., Rustagi Vineeta, Patel Monika, Tiwari Rakesh K.: On Water: Silver-Catalyzed Domino Approach for the Synthesis of Benzoxazine/Oxazine-Fused Isoquinolines and Naphthyridines from o-Alkynyl Aldehydes. J. Org. Chem. 2013, 78, 6657. <http://dx.doi.org/10.1021/jo4009639>
• Yang Xin, Xue Ying: QM/MM investigation on 1,3-dipolar cycloadditions of the phthalazinium dicyanomethanide with three different dipolarophiles on water and in solution. Phys. Chem. Chem. Phys. 2013, 15, 11846. <http://dx.doi.org/10.1039/c3cp51048d>
• Pinto Joana, Silva Vera L. M., Silva Ana M. G., Silva Artur M. S., Costa José C. S., Santos Luís M. N. B. F., Enes Roger, Cavaleiro José A. S., Vicente António A. M. O. S., Teixeira José A. C.: Ohmic heating as a new efficient process for organic synthesis in water. Green Chem. 2013, 15, 970. <http://dx.doi.org/10.1039/c3gc36881e>
• Merchán Arenas Diego R., Martínez Bonilla Carlos A., Kouznetsov Vladimir V.: Aqueous SDS micelle-promoted acid-catalyzed domino ABB′ imino Diels–Alder reaction: a mild and efficient synthesis of privileged 2-methyl-tetrahydroquinoline scaffolds. Org. Biomol. Chem. 2013, 11, 3655. <http://dx.doi.org/10.1039/c3ob40171e>
• Nobuoka Kaoru, Kitaoka Satoshi, Yanagisako Atsuki, Maki Yusuke, Harran Thomas, Ishikawa Yuichi: Stereoselectivity of the Diels–Alder reaction in ionic liquids with cyano moieties: effect of the charge delocalization of anions on the relation of solvent–solvent and solute–solvent interactions. RSC Adv. 2013, 3, 19632. <http://dx.doi.org/10.1039/c3ra43523g>
• Rustagi Vineeta, Tiwari Rakesh, Verma Akhilesh Kumar: AgI-Catalyzed Cascade Strategy: Regioselective Access to Diversely Substituted Fused Benzimidazo[2,1-a]isoquinolines, Naphthyridines, Thienopyridines, and Quinoxalines in Water. Eur. J. Org. Chem. 2012, 2012, 4590. <http://dx.doi.org/10.1002/ejoc.201200546>
• Pinto Atahualpa, Boddy Christopher N.: Non-canonical regioisomerizations and a ‘Diels–Alderase’ are likely essential in the biosynthesis of Spiculoic acid A. Bioorganic & Medicinal Chemistry Letters 2012, 22, 5253. <http://dx.doi.org/10.1016/j.bmcl.2012.06.052>
• Syska Hitrisia, Herrmann Wolfgang A., Kühn Fritz E.: Water-soluble carbene complexes as catalysts for the hydrogenation of acetophenone under hydrogen pressure. J Organomet Chem 2012, 703, 56. <http://dx.doi.org/10.1016/j.jorganchem.2012.01.001>
• Verma Girijesh K., Raghuvanshi Keshav, Kumar Ram, Singh Maya Shankar: An efficient one-pot three-component synthesis of functionalized pyrimido[4,5-b]quinolines and indeno fused pyrido[2,3-d]pyrimidines in water. Tetrahetron Lett 2012, 53, 399. <http://dx.doi.org/10.1016/j.tetlet.2011.11.047>
• Chang Meng-Yang, Wu Ming-Hao: Synthesis of tetrahydroanthracen-9-ones by the domino aldol condensation/Diels–Alder cycloaddition. Tetrahedron Letters 2012, 53, 3173. <http://dx.doi.org/10.1016/j.tetlet.2012.04.053>
• Glassner Mathias, Delaittre Guillaume, Kaupp Michael, Blinco James P., Barner-Kowollik Christopher: (Ultra)Fast Catalyst-Free Macromolecular Conjugation in Aqueous Environment at Ambient Temperature. S J Am Chem Soc 2012, 134, 7274. <http://dx.doi.org/10.1021/ja301762y>
• Jin Zhichao, Yang Ruojie, Du Yu, Tiwari Bhoopendra, Ganguly Rakesh, Chi Yonggui Robin: Enantioselective Intramolecular Formal [2 + 4] Annulation of Acrylates and α,β-Unsaturated Imines Catalyzed by Amino Acid Derived Phosphines. Org. Lett. 2012, 14, 3226. <http://dx.doi.org/10.1021/ol3013588>
• He Yan, Zhang Xinying, Cui Liangyan, Wang Jianji, Fan Xuesen: Catalyst-free synthesis of diversely substituted 6H-benzo[c]chromenes and 6H-benzo[c]chromen-6-ones in aqueous media under MWI. Green Chem. 2012, 14, 3429. <http://dx.doi.org/10.1039/c2gc36379h>
• Tang Shi-Ya, Shi Jing, Guo Qing-Xiang: Accurate prediction of rate constants of Diels–Alder reactions and application to design of Diels–Alder ligation. Biomol Chem 2012, 10, 2673. <http://dx.doi.org/10.1039/c2ob07079k>
• Khalafy Jabbar, Rimaz Mehdi, Ezzati Mahnaz, Prager Rolf H.: A Green One-Pot Protocol for Regioselective Synthesis of New Substituted 7,8-Dihydrocinnoline-5(6H)-ones. Bulletin of the Korean Chemical Society 2012, 33, 2890. <http://dx.doi.org/10.5012/bkcs.2012.33.9.2890>
• Benchouk W., Mekelleche S. M., Silvi B., Aurell M. J., Domingo L. R.: Understanding the kinetic solvent effects on the 1,3-dipolar cycloaddition of benzonitrile N-oxide: a DFT study. J Phys Org Chem 2011, 24, 611. <http://dx.doi.org/10.1002/poc.1858>
• Ozawa Takuya, Kurahashi Takuya, Matsubara Seijiro: Dehydrogenative Diels–Alder Reaction. Org Lett 2011, 13, 5390. <http://dx.doi.org/10.1021/ol202283d>
• Bittner Bożena, Janus Ewa, Milchert Eugeniusz: N-hexylpyridinium bis(trifluoromethylsulfonyl)imide and Lewis acids — catalytic systems for Diels-Alder reaction. cent eur j chem 2011, 9, 192. <http://dx.doi.org/10.2478/s11532-010-0138-4>
• Meir Rinat, Chen Hui, Lai Wenzhen, Shaik Sason: Oriented Electric Fields Accelerate Diels–Alder Reactions and Control the endo/exo Selectivity. Chem Eur J of Chem Phys 2010, 11, 301. <http://dx.doi.org/10.1002/cphc.200900848>
• Lim Reyna K. V., Lin Qing: Bioorthogonal chemistry: a covalent strategy for the study of biological systems. Sci China Chem 2010, 53, 61. <http://dx.doi.org/10.1007/s11426-010-0020-4>
• James Olusola O., Maity Sudip, Usman Lamidi Ajao, Ajanaku Kolawole O., Ajani Olayinka O., Siyanbola Tolu O., Sahu Satanand, Chaubey Rashmi: Towards the conversion of carbohydrate biomass feedstocks to biofuels via hydroxylmethylfurfural. Energy Environ Sci 2010, 3, 1833. <http://dx.doi.org/10.1039/b925869h>
• Chiappe Cinzia, Malvaldi Marco, Pomelli Christian Silvio: The solvent effect on the Diels–Alder reaction in ionic liquids: multiparameter linear solvation energy relationships and theoretical analysis. Green Chem 2010, 12, 1330. <http://dx.doi.org/10.1039/c0gc00074d>
• Kleiner Christian M., Horst Luise, Würtele Christian, Wende Raffael, Schreiner Peter R.: Isolation of the key intermediates in the catalyst-free conversion of oxiranes to thiiranes in water at ambient temperature. Org Biomol Chem 2009, 7, 1397. <http://dx.doi.org/10.1039/b820232j>
• Das Bhaskar C., Mahalingam Sakkarapalayam M., Evans Todd, Kabalka George W., Anguiano J., Hema K.: Design and synthesis of (E)-1-((3-ethyl-2,4,4-trimethylcyclohex-2-enylidene)methyl-4-substituted benzenes from 1-(2,6,6-trimethylcyclohex-1-enyl)ethanol. Chem Commun 2009, 2133. <http://dx.doi.org/10.1039/b823063c>
• Leclercq Loïc, Schmitzer Andreea R.: Supramolecular effects involving the incorporation of guest substrates in imidazolium ionic liquid networks: Recent advances and future developments. Supramol Chem 2009, 21, 245. <http://dx.doi.org/10.1080/10610270802468421>
• Sharma Gaurav, Kumar Raj, Chakraborti Asit K.: ‘On water’ synthesis of 2,4-diaryl-2,3-dihydro-1,5-benzothiazepines catalysed by sodium dodecyl sulfate (SDS). Tetrahetron Lett 2008, 49, 4269. <http://dx.doi.org/10.1016/j.tetlet.2008.04.146>
• Ahlford Katrin, Lind Jesper, Mäler Lena, Adolfsson Hans: Rhodium-catalyzed asymmetric transfer hydrogenation of alkyl and aryl ketones in aqueous media. Green Chem 2008, 10, 832. <http://dx.doi.org/10.1039/b806177g>
• Reinhardt Denise, Ilgen Florian, Kralisch Dana, König Burkhard, Kreisel Günter: Evaluating the greenness of alternative reaction media. Green Chem 2008, 10, 1170. <http://dx.doi.org/10.1039/b807379a>
• Tiwari Shraeddha, Kumar Anil: Unusual temperature dependence of salt effects for “on water” Wittig reaction: hydrophobicity at the interface. Chem Commun 2008, 4445. <http://dx.doi.org/10.1039/b809127g>
• Windmon Nicole, Dragojlovic Veljko: Diels-Alder reactions in the presence of a minimal amount of water. Green Chem Lett & Revs 2008, 1, 155. <http://dx.doi.org/10.1080/17518250802482505>
• Mihovilovic Marko D: Stereoselective hybrid catalysts: new opportunities. J Chem Technol Biotechnol 2007, 82, 1067. <http://dx.doi.org/10.1002/jctb.1752>
• Anderson James A., McKenna Fiona-Mairead, Linares-Solano Angel, Wells Richard P. K.: Use of Water as a Solvent in Directing Hydrogenation Reactions of Aromatic Acids over Pd/carbon Nanofibre Catalysts. Catal Lett 2007, 119, 16. <http://dx.doi.org/10.1007/s10562-007-9207-5>
• Basaif Salem A., Hassan Mohamed A., Gobouri Adil A.: AlCl3-Catalyzed diazocoupling of 1-(aryl/hetaryl)-3-phenyl-1H-pyrazol-2-in-5-ones in aqueous medium. Synthesis of hetaryl-azopyrazolones and their application as disperse dyes. J Dye Pig 2007, 72, 387. <http://dx.doi.org/10.1016/j.dyepig.2005.09.025>
• Roelfes Gerard: DNA and RNA induced enantioselectivity in chemical synthesis. Mol Biosyst 2007, 3, 126. <http://dx.doi.org/10.1039/b614527b>
• Käss Steffen, Gregor Thomas, Kersting Berthold: Diels-Alder Reactivity of Binuclear Complexes with Calixarene-like Structures. Angew Chem 2006, 118, 107. <http://dx.doi.org/10.1002/ange.200500683>
• Käss Steffen, Gregor Thomas, Kersting Berthold: Diels-Alder Reactivity of Binuclear Complexes with Calixarene-like Structures. Angew Chem Int Ed 2006, 45, 101. <http://dx.doi.org/10.1002/anie.200500683>
• Walde Peter: Surfactant Assemblies and their Various Possible Roles for the Origin(S) of Life. Orig Life Evol Biosph 2006, 36, 109. <http://dx.doi.org/10.1007/s11084-005-9004-3>
• Wang Guan-Wu, Miao Chun-Bao: Environmentally benign one-pot multi-component approaches to the synthesis of novel unsymmetrical 4-arylacridinediones. Green Chem 2006, 8, 1080. <http://dx.doi.org/10.1039/b604064k>
• CHEMOURI H., MEKELLECHE S. M.: AN ANALYSIS OF THE REGIOSELECTIVITY IN HETERO DIELS–ALDER REACTIONS USING DFT-BASED REACTIVITY INDEXES. J. Theor. Comput. Chem. 2006, 05, 197. <http://dx.doi.org/10.1142/S0219633606002210>
• Rispens Theo, Engberts Jan B. F. N.: Kinetic solvent effects on 1,3-dipolar cycloadditions of benzonitrile oxide. J Phys Org Chem 2005, 18, 908. <http://dx.doi.org/10.1002/poc.917>
• Rispens Theo, Engberts Jan B. F. N.: Cycloadditions in mixed aqueous solvents: the role of the water concentration. J. Phys. Org. Chem. 2005, 18, 725. <http://dx.doi.org/10.1002/poc.926>
• Mahindaratne Mathew P.D., Quiñones Brian A., Recio Antonio, Rodriguez Eric A., Lakner Frederick J., Negrete George R.: Salt, concentration, and temperature effects on an asparagine-based, aqueous Diels–Alder cycloaddition. Tetrahedron 2005, 61, 9495. <http://dx.doi.org/10.1016/j.tet.2005.08.003>
• Imperato Giovanni, Eibler Ernst, Niedermaier Julia, König Burkhard: Low-melting sugar–urea–salt mixtures as solvents for Diels–Alder reactions. Chem Commun 2005, 1170. <http://dx.doi.org/10.1039/b414515a>
• Calvet Géraldine, Guillot Régis, Blanchard Nicolas, Kouklovsky Cyrille: Intermolecular nitroso Diels–Alder cycloaddition of α-acetoxynitroso derivatives in aqueous medium. Org Biomol Chem 2005, 3, 4395. <http://dx.doi.org/10.1039/b513397a>
• Leininger Neil F., Gainer John L., Kirwan Donald J.: Effect of aqueous PEG or PPG solvents on reaction selectivity and Gibbs energies. AIChE 2004, 50, 511. <http://dx.doi.org/10.1002/aic.10044>
• Chen I-Hon, Young Jun-Nan, Yu Shuchun Joyce: Recyclable organotungsten Lewis acid and microwave assisted Diels–Alder reactions in water and in ionic liquids. Tetrahedron 2004, 60, 11903. <http://dx.doi.org/10.1016/j.tet.2004.09.078>
• Lomberget Thierry, Chataigner Isabelle, Bouyssi Didier, Maddaluno Jacques, Balme Geneviève: Diels–Alder cycloadditions of functionalized (Z)-1-benzylidene-2-methylene cyclohexanes: the beneficial effect of high pressure. Tetrahetron Lett 2004, 45, 3437. <http://dx.doi.org/10.1016/j.tetlet.2004.03.010>
• Kanosue Yoshifumi, Kojima Satoshi, Hiraga Yoshikazu, Ohkata Katsuo: Relationship between the Hydrophobicity of Dipeptides and the Michaelis–Menten Constant Km of Their Hydrolysis by Carboxypeptidase-Y and Carboxypeptidase-A. Bull Chem Soc Jpn 2004, 77, 1187. <http://dx.doi.org/10.1246/bcsj.77.1187>
• Leininger Neil F., Clontz Reid, Gainer John L., Kirwan Donald J.: Polyethylene glycol-water and polypropylene glycol-water solutionsas benign reaction solvents. Chem Eng Com 2003, 190, 431. <http://dx.doi.org/10.1080/00986440302082>
• Li Chaomin, Bardhan Sujata, Pace Emily A., Liang Mei-Chih, Gilmore Thomas D., Porco John A.: Angiogenesis Inhibitor Epoxyquinol A:  Total Synthesis and Inhibition of Transcription Factor NF-κB. Org Lett 2002, 4, 3267. <http://dx.doi.org/10.1021/ol026513n>
• Otto Sijbren, Engberts Jan B. F. N.: ChemInform Abstract: Diels-Alder Reactions in Water. ChemInform 2001, 32, no. <http://dx.doi.org/10.1002/chin.200113283>