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Pure Appl. Chem., 2001, Vol. 73, No. 1, pp. 103-111

http://dx.doi.org/10.1351/pac200173010103

Catalysis for green chemistry

James H. Clark

Clean Technology Centre, Department of Chemistry, University of York, York YO10 5DD, UK

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  • Zhang Jingli, Zhang Mingxi, Tang Kangjian, Verpoort Francis, Sun Taolei: Polymer-Based Stimuli-Responsive Recyclable Catalytic Systems for Organic Synthesis. Small 2014, 10, 32. <http://dx.doi.org/10.1002/smll.201300287>
  • Bosica Giovanna, Spiteri Jonathan, Borg Caroline: Aza-Michael reaction: selective mono- versus bis-addition under environmentally-friendly conditions. Tetrahedron 2014, 70, 2449. <http://dx.doi.org/10.1016/j.tet.2014.02.021>
  • Rahman Matiur, Sarkar Anirban, Ghosh Monoranjan, Majee Adinath, Hajra Alakananda: Catalytic application of task specific ionic liquid on the synthesis of benzoquinazolinone derivatives by a multicomponent reaction. Tetrahedron Letters 2014, 55, 235. <http://dx.doi.org/10.1016/j.tetlet.2013.11.011>
  • Shaikh Isak Rajjak: Organocatalysis: Key Trends in Green Synthetic Chemistry, Challenges, Scope towards Heterogenization, and Importance from Research and Industrial Point of View. Journal of Catalysts 2014, 2014, 1. <http://dx.doi.org/10.1155/2014/402860>
  • Prakash Praveen, Jijy Eliyan, Preethanuj Preethalayam, Pihko Petri M., Sarath Chand Sarngadharan, Radhakrishnan Kokkuvayil V.: Palladium-Catalyzed Skeletal Rearrangement of Spirotricyclic Olefins: A Facile One-Pot Strategy for the Synthesis of a Novel Motif with Cyclopentene Fused to Benzofuran and Pyrazolidine. Chem. Eur. J. 2013, 19, 10473. <http://dx.doi.org/10.1002/chem.201301475>
  • Dadiboyena Sureshbabu, Hamme Ashton T.: Environmentally Benign Lewis Acid Promoted [2+3] Dipolar Cycloaddition Reactions of Nitrile Imines with Alkenes in Water. Eur. J. Org. Chem. 2013, 2013, 7567. <http://dx.doi.org/10.1002/ejoc.201300840>
  • Ramananarivo Hugo Ronald, Solhy Abderrahim, Sebti Jalila, Smahi Abedlatif, Zahouily Mohamed, Clark James, Sebti Said: An Eco-Friendly Paradigm for the Synthesis of α-Hydroxyphosphonates Using Sodium-Modified Fluorapatite under Solventless Conditions. ACS Sustainable Chem. Eng. 2013, 1, 403. <http://dx.doi.org/10.1021/sc3001417>
  • REKHA M., HAMZA A., VENUGOPAL B.R., NAGARAJU N.: Synthesis of 2-Substituted Benzimidazoles and 1,5-Disubstituted Benzodiazepines on Alumina and Zirconia Catalysts. Chinese Journal of Catalysis 2012, 33, 439. <http://dx.doi.org/10.1016/S1872-2067(11)60338-0>
  • Altman E., Stefanidis G. D., van Gerven T., Stankiewicz A.: Microwave-Promoted Synthesis of n-Propyl Propionate using Homogeneous Zinc Triflate Catalyst. Industrial Eng Chem Res 2012, 51, 1612. <http://dx.doi.org/10.1021/ie200687m>
  • Kumar Dinesh, Kommi Damodara N., Bollineni Narendra, Patel Alpesh R., Chakraborti Asit K.: Catalytic procedures for multicomponent synthesis of imidazoles: selectivity control during the competitive formation of tri- and tetrasubstituted imidazoles. Green Chem. 2012, 14, 2038. <http://dx.doi.org/10.1039/c2gc35277j>
  • Wang Xue, Chen Lifang, Shang Meng, Lin Feng, Hu Juncheng, Richards Ryan M: Nanoscale gold intercalated into mesoporous silica as a highly active and robust catalyst. Nanotechnology 2012, 23, 294010. <http://dx.doi.org/10.1088/0957-4484/23/29/294010>
  • Vernekar Varsha U., Hosamani Kallappa M., Shaikh Irfan N., Achar Kavitha C.S.: PTA (H3PO4��12WO3��xH2O): An eco-friendly catalyst for the synthesis of new Schiff-bases containing benzimidazole moiety. Arabian Journal of Chemistry 2011. <http://dx.doi.org/10.1016/j.arabjc.2011.07.030>
  • Solhy Abderrahim, Amer Walid, Karkouri Mohamed, Tahir Rachid, El Bouari Abdeslam, Fihri Aziz, Bousmina Mostapha, Zahouily Mohamed: Bi-functional modified-phosphate catalyzed the synthesis of α-α′-(EE)-bis(benzylidene)-cycloalkanones: Microwave versus conventional-heating. Journal of Molecular Catalysis A: Chemical 2011, 336, 8. <http://dx.doi.org/10.1016/j.molcata.2010.11.032>
  • Marvi Omid, Alizadeh Abdolhamid, Zarrabi Saeid: Montmorillonite K-10 Clay as an Efficient Reusable Heterogeneous Catalyst for the Solvent-Free Microwave Mediated Synthesis of 5-Substituted 1H-Tetrazoles. Bull Kor Chem Soc 2011, 32, 4001. <http://dx.doi.org/10.5012/bkcs.2011.32.11.4001>
  • Clark James H.: ChemInform Abstract: Catalysis for Green Chemistry. ChemInform 2010, 32, no. <http://dx.doi.org/10.1002/chin.200138272>
  • Khurana Jitender M., Kumar Sanjay: Ionic liquid: an efficient and recyclable medium for the synthesis of octahydroquinazolinone and biscoumarin derivatives. Monatshefte für Chemie 2010, 141, 561. <http://dx.doi.org/10.1007/s00706-010-0306-4>
  • Cai Zhen-Yu, Zhu Ming-Qiao, Chen Jun, Shen Yang-Yi, Zhao Jing, Tang Yue, Chen Xin-Zhi: Solvent-free oxidation of cyclohexene over catalysts Au/OMS-2 and Au/La-OMS-2 with molecular oxygen. Catal Commun 2010, 12, 197. <http://dx.doi.org/10.1016/j.catcom.2010.09.014>
  • Keri Rangappa S., Hosamani Kallappa M., Seetharama Reddy Harisha R.: A Solvent-Free Synthesis of Coumarins Using Phosphotungstic Acid as Catalyst. Catal Lett 2009, 131, 321. <http://dx.doi.org/10.1007/s10562-009-9940-z>
  • Keri Rangappa S., Hosamani Kallappa M., Seetharama Reddy Harisha R., Shingalapur Ramya V.: Wells–Dawson Heteropolyacid: An Efficient Recyclable Catalyst for the Synthesis of Benzimidazoles Under Microwave Condition. Catal Lett 2009, 131, 552. <http://dx.doi.org/10.1007/s10562-009-9966-2>
  • Pathak Vijai N., Varshney Bindu, Gupta Ragini: A ‘one pot’ synthesis of 2-aryl-4H-1-benzopyran-4-ones under coupled microwave phase transfer catalysis (PTC) and ultrasonic irradiation PTC. J Heterocyclic Chem 2008, 45, 589. <http://dx.doi.org/10.1002/jhet.5570450246>
  • Steffen Rafael Augusto, Teixeira Sergio, Sepulveda Jorge, Rinaldi Roberto, Schuchardt Ulf: Alumina-catalyzed Baeyer–Villiger oxidation of cyclohexanone with hydrogen peroxide. Journal of Molecular Catalysis A 2008, 287, 41. <http://dx.doi.org/10.1016/j.molcata.2008.02.021>
  • Sharma Gaurav, Kumar Raj, Chakraborti Asit K.: Fluoroboric acid adsorbed on silica-gel (HBF4–SiO2) as a new, highly efficient and reusable heterogeneous catalyst for thia-Michael addition to α,β-unsaturated carbonyl compounds. Tetrahetron Lett 2008, 49, 4272. <http://dx.doi.org/10.1016/j.tetlet.2008.04.144>
  • Dawson T L: It must be green: meeting society’s environmental concerns. Coloration Technol 2008, 124, 67. <http://dx.doi.org/10.1111/j.1478-4408.2008.00124.x>
  • Tayebee Reza, Alizadeh Mohammad Hassan: Environmentally Benign Oxidation of Some Organic Sulfides with 34% Hydrogen Peroxide Catalyzed by Simple Heteropolyoxometalates. Chin J Chem 2007, 25, 1340. <http://dx.doi.org/10.1002/cjoc.200790249>
  • Vasiliev Aleksey N., Golovko Leonid V., Povazhny Vladimir A., Zlotnikov Eugene, Chen Jengshiou, Khinast Johannes G.: Functionalized nanoporous carbon as a catalyst for Suzuki coupling reactions. Microp Mesop Mat 2007, 101, 342. <http://dx.doi.org/10.1016/j.micromeso.2006.11.026>
  • Sharma Gaurav, Kumar Raj, Chakraborti Asit K.: A novel environmentally friendly process for carbon–sulfur bond formation catalyzed by montmorillonite clays. Journal of Molecular Catalysis A 2007, 263, 143. <http://dx.doi.org/10.1016/j.molcata.2006.08.021>
  • Kidwai Mazaahir, Bansal Vikas, Mothsra Poonam, Saxena Shilpi, Somvanshi Rishi K., Dey Sharmistha, Singh Tej P.: Molecular iodine: A versatile catalyst for the synthesis of bis(4-hydroxycoumarin) methanes in water. Journal of Molecular Catalysis A 2007, 268, 76. <http://dx.doi.org/10.1016/j.molcata.2006.11.054>
  • Karimi Babak, Ghoreishi-Nezhad Maryam: Highly chemoselective acetalization of carbonyl compounds catalyzed by a novel recyclable ammonium triflate-functionalized silica. Journal of Molecular Catalysis A 2007, 277, 262. <http://dx.doi.org/10.1016/j.molcata.2007.08.001>
  • Yadav Mukesh Kr., Jasra Raksh V.: Synthesis of nopol from β-pinene using ZnCl2 impregnated Indian Montmorillonite. Catal Commun 2006, 7, 889. <http://dx.doi.org/10.1016/j.catcom.2006.04.002>
  • Thomas Bejoy, Das Bibhuti B., Sugunan S.: Rare earth exchanged (Ce3+, La3+ and RE3+) H–Y zeolites as solid acid catalysts for the synthesis of linear alkyl benzenes. Microp Mesop Mat 2006, 95, 329. <http://dx.doi.org/10.1016/j.micromeso.2006.05.035>
  • Thomas Bejoy, Sugunan S.: Rare-earth (Ce3+, La3+, Sm3+, and RE3+) exchanged Na-Y zeolites and K-10 clay as solid acid catalysts for the synthesis of benzoxazole via Beckmann rearrangement of salicylaldoxime. Microp Mesop Mat 2006, 96, 55. <http://dx.doi.org/10.1016/j.micromeso.2006.06.005>
  • Singh R., Geetanjali: Solvent-free regioselective synthesis of 6-and 7-substituted pteridines under microwave irradiation. Russ J Org Chem 2006, 42, 136. <http://dx.doi.org/10.1134/S1070428006010210>
  • Salvador Jorge A.R., Silvestre Samuel M.: Bismuth-catalyzed allylic oxidation using t-butyl hydroperoxide. Tetrahetron Lett 2005, 46, 2581. <http://dx.doi.org/10.1016/j.tetlet.2005.02.080>
  • Karimi Babak, Ghoreishi-Nezhad Maryam, Clark James H.: Selective Oxidation of Sulfides to Sulfoxides Using 30% Hydrogen Peroxide Catalyzed with a Recoverable Silica-Based Tungstate Interphase Catalyst. Org Lett 2005, 7, 625. <http://dx.doi.org/10.1021/ol047635d>
  • Rajabi Fatemeh, Clark James H, Karimi Babak, Macquarrie Duncan J: The selective aerobic oxidation of methylaromatics to benzaldehydes using a unique combination of two heterogeneous catalysts. Org Biomol Chem 2005, 3, 725. <http://dx.doi.org/10.1039/b419322a>
  • Samanta Sujit, Mal Nawal Kishor, Manna Abhijit, Bhaumik Asim: Mesoporous tin silicate: an efficient liquid phase oxidative dehydrogenation catalyst. Appl Catal A Gen 2004, 273, 157. <http://dx.doi.org/10.1016/j.apcata.2004.06.025>
  • Serwicka Ewa M., Bahranowski Krzysztof: Environmental catalysis by tailored materials derived from layered minerals. Catal Today 2004, 90, 85. <http://dx.doi.org/10.1016/j.cattod.2004.04.012>
  • Samanta S., Laha S.C., Mal N.K., Bhaumik A.: Co(III)-containing mesoporous silica as an efficient catalyst in selective dihydroxylation of cyclohexene. Journal of Molecular Catalysis A 2004, 222, 235. <http://dx.doi.org/10.1016/j.molcata.2004.08.014>
  • Bellesia Franco, De Buyck Laurent, Ghelfi Franco, Pagnoni Ugo M., Strazzolini Paolo: Oxidation of Aliphatic 2,2‐Dichloroalkanals by HNO3 in CH2Cl2: An Easy and Eco‐friendly Route to the Corresponding 2,2‐Dichloroalkanoic Acids. Synth Common 2004, 34, 1473. <http://dx.doi.org/10.1081/SCC-120030698>
  • Chauhan S. M. S., Singh Ram, Geetanjali: Microwave-Assisted Synthesis of 10-Substituted Isoalloxazines in the Presence of Solid Acids. Synth Common 2003, 33, 1179. <http://dx.doi.org/10.1081/SCC-120017194>
  • Chauhan Shive M. S., Srinivas Kandadai A., Srivastava Pravin K., Sahoo Bishawabhusan: Solvent-free synthesis of phthalocyanines. J. Porphyrins Phthalocyanines 2003, 07, 548. <http://dx.doi.org/10.1142/S1088424603000689>
  • Bergbreiter David E., Osburn Philip L., Li Chunmei: Soluble Polymer-Supported Catalysts Containing Azo Dyes. Org Lett 2002, 4, 737. <http://dx.doi.org/10.1021/ol017198s>