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Pure Appl. Chem., 2000, Vol. 72, No. 7, pp. 1207-1228

http://dx.doi.org/10.1351/pac200072071207

Synthetic pathways and processes in green chemistry. Introductory overview

Pietro Tundo*, Paul Anastas, David StC. Black, Joseph Breen, Terrence Collins, Sofia Memoli, Junshi Miyamoto, Martyn Polyakoff and William Tumas

Università Ca' Foscari di Venezia, Dipartimento di Scienze Ambientali, Dorsoduro 2137 Venice, Italy.

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  • 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>
  • Pal Gargi, Paul Sanjay, Ghosh Partha Pratim, Das Asish R.: PhIO promoted synthesis of nitrile imines and nitrile oxides within a micellar core in aqueous media: a regiocontrolled approach to synthesizing densely functionalized pyrazole and isoxazoline derivatives. RSC Adv. 2014, 4, 8300. <http://dx.doi.org/10.1039/c3ra46129g>
  • Tada Kazuya: Optimization of photovoltaic device based on poly(3-hexylthiophene):C60bulk heterojunction composites prepared with halogen-free solvent. Jpn. J. Appl. Phys. 2014, 53, 01AB01. <http://dx.doi.org/10.7567/JJAP.53.01AB01>
  • Morlot Julien, Uyttebroeck Nicolas, Agustin Dominique, Poli Rinaldo: Solvent-Free Epoxidation of Olefins Catalyzed by “[MoO2 (SAP)]”: A New Mode of tert -Butylhydroperoxide Activation. ChemCatChem 2013, 5, 601. <http://dx.doi.org/10.1002/cctc.201200068>
  • Zhang Hong-ming, Wang Xian-hong: Eco-friendly water-borne conducting polyaniline. Chin J Polym Sci 2013, 31, 853. <http://dx.doi.org/10.1007/s10118-013-1287-7>
  • Wang Leilei, Huang Manna, Zhu Xinhai, Wan Yiqian: Polyethylene glycol (PEG-200)-promoted sustainable one-pot three-component synthesis of 3-indole derivatives in water. Applied Catalysis A: General 2013, 454, 160. <http://dx.doi.org/10.1016/j.apcata.2012.12.008>
  • Spietelun Agata, Marcinkowski Łukasz, de la Guardia Miguel, Namieśnik Jacek: Recent developments and future trends in solid phase microextraction techniques towards green analytical chemistry. Journal of Chromatography A 2013, 1321, 1. <http://dx.doi.org/10.1016/j.chroma.2013.10.030>
  • Prasad Davinder, Preetam Amreeta, Nath Mahendra: DBSA catalyzed cyclotrimerization of acetophenones: An efficient synthesis of 1,3,5-triarylbenzenes under solvent-free conditions. Comptes Rendus Chimie 2013, 16, 252. <http://dx.doi.org/10.1016/j.crci.2012.12.008>
  • Da Silva Éric, Dayoub Wissam, Duguet Nicolas, Métay Estelle, Popowycz Florence, Lemaire Marc: New research areas inspired by sustainable development. Comptes Rendus Chimie 2013, 16, 343. <http://dx.doi.org/10.1016/j.crci.2012.12.019>
  • Morcelle Susana R., Cánepa Alicia S., Padró Juan M., Llerena-Suster Carlos R., Clapés Pere: Syntheses of dipeptide alcohols and dipeptide aldehyde precursors catalyzed by plant cysteine peptidases. Journal of Molecular Catalysis B: Enzymatic 2013, 89, 130. <http://dx.doi.org/10.1016/j.molcatb.2012.12.004>
  • Lozano Rodrigo, Carpenter Angela, Satric Vojislavka: Fostering green chemistry through a collaborative business model: A Chemical Leasing case study from Serbia. Resources, Conservation and Recycling 2013, 78, 136. <http://dx.doi.org/10.1016/j.resconrec.2013.07.007>
  • Tada Kazuya: Yet another poor man's green bulk heterojunction photocells: Annealing effect and film composition dependence of photovoltaic devices using poly(3-hexylthiophene):C70 composites prepared with chlorine-free solvent. Solar Energy Materials and Solar Cells 2013, 108, 82. <http://dx.doi.org/10.1016/j.solmat.2012.09.014>
  • Tada Kazuya: Bulk heterojunction photocells utilizing neat C70 and low energy-gap polymer prepared with halogen-free solvent. Solar Energy Materials and Solar Cells 2013, 117, 194. <http://dx.doi.org/10.1016/j.solmat.2013.06.004>
  • Pradhan Koyel, Paul Sanjay, Das Asish R.: Fe(DS)3, an efficient Lewis acid-surfactant-combined catalyst (LASC) for the one pot synthesis of chromeno[4,3-b]chromene derivatives by assembling the basic building blocks. Tetrahedron Letters 2013, 54, 3105. <http://dx.doi.org/10.1016/j.tetlet.2013.04.001>
  • Thurow Samuel, Webber Rodrigo, Perin Gelson, Lenardão Eder J., Alves Diego: Glycerol/hypophosphorous acid: an efficient system solvent-reducing agent for the synthesis of 2-organylselanyl pyridines. Tetrahedron Letters 2013, 54, 3215. <http://dx.doi.org/10.1016/j.tetlet.2013.04.057>
  • Subramanian Thirumeni, Dhakshinamoorthy Amarajothi, Pitchumani Kasi: Amino acid intercalated layered double hydroxide catalyzed chemoselective methylation of phenols and thiophenols with dimethyl carbonate. Tetrahedron Letters 2013, 54, 7167. <http://dx.doi.org/10.1016/j.tetlet.2013.10.098>
  • Tayebee Reza, Rezaei Seresht Esmail, Jafari Fariba, Rabiei Sima: Simple Methodology for the Aerobic N-Methylation of Substituted Anilines Catalyzed by Zirconium Oxychloride Octahydrate, ZrOCl2·8H2O. Ind. Eng. Chem. Res. 2013, 52, 11001. <http://dx.doi.org/10.1021/ie4018786>
  • Agee Brian M., Mullins Gene, Swartling Daniel J.: Friedel–Crafts Acylation Using Solar Irradiation. ACS Sustainable Chem. Eng. 2013, 1, 1580. <http://dx.doi.org/10.1021/sc4002802>
  • Gawande Manoj B., Bonifácio Vasco D. B., Luque Rafael, Branco Paula S., Varma Rajender S.: Benign by design: catalyst-free in-water, on-water green chemical methodologies in organic synthesis. Chem. Soc. Rev. 2013, 42, 5522. <http://dx.doi.org/10.1039/c3cs60025d>
  • Kommi Damodara N., Kumar Dinesh, Chakraborti Asit K.: “All water chemistry” for a concise total synthesis of the novel class anti-anginal drug (RS), (R), and (S)-ranolazine. Green Chem. 2013, 15, 756. <http://dx.doi.org/10.1039/c3gc36997h>
  • Kommi Damodara N., Jadhavar Pradeep S., Kumar Dinesh, Chakraborti Asit K.: “All-water” one-pot diverse synthesis of 1,2-disubstituted benzimidazoles: hydrogen bond driven ‘synergistic electrophile–nucleophile dual activation’ by water. Green Chem. 2013, 15, 798. <http://dx.doi.org/10.1039/c3gc37004f>
  • Kumar Dinesh, Sonawane Mukesh, Pujala Brahmam, Jain Varun K., Bhagat Srikant, Chakraborti Asit K.: Supported protic acid-catalyzed synthesis of 2,3-disubstituted thiazolidin-4-ones: enhancement of the catalytic potential of protic acid by adsorption on solid supports. Green Chem. 2013, 15, 2872. <http://dx.doi.org/10.1039/c3gc41218k>
  • Guérin Béatrice, Fernandes Daniel Mesquita, Daran Jean-Claude, Agustin Dominique, Poli Rinaldo: Investigation of induction times, activity, selectivity, interface and mass transport in solvent-free epoxidation by H2O2 and TBHP: a study with organic salts of the [PMo12O40]3− anion. New J. Chem. 2013, 37, 3466. <http://dx.doi.org/10.1039/c3nj00523b>
  • Kumar Atul, Saxena Deepti, Gupta Maneesh Kumar: Boric acid catalyzed Ugi three-component reaction in aqueous media. RSC Adv. 2013, 3, 4610. <http://dx.doi.org/10.1039/c3ra23087b>
  • Kumar Dinesh, Seth Kapileswar, Kommi Damodara N., Bhagat Srikant, Chakraborti Asit K.: Surfactant micelles as microreactors for the synthesis of quinoxalines in water: scope and limitations of surfactant catalysis. RSC Adv. 2013, 3, 15157. <http://dx.doi.org/10.1039/c3ra41038b>
  • Halimehjani Azim Ziyaei, Karimi Nafiseh, Saidi Mohammad R.: Michael Addition Reaction of Anthrone to Nitroolefins in Water. Synthetic Communications 2013, 43, 744. <http://dx.doi.org/10.1080/00397911.2011.608479>
  • Cheraiet Zinelaabidine, Hessainia Sihem, Ouarna Souad, Berredjem Malika, Aouf Nour-Eddine: A simple and eco-sustainable method for the O-Boc protection/deprotection of various phenolic structures under water-mediated/catalyst-free conditions. Green Chemistry Letters and Reviews 2013, 1. <http://dx.doi.org/10.1080/17518253.2012.738371>
  • Wada Kenji, Miura Hiroki, Hosokawa Saburo, Inoue Masashi: Development of Ceria-supported Ruthenium Catalysts for Green Organic Transformation Processes. J. Jpn. Petrol. Inst. 2013, 56, 69. <http://dx.doi.org/10.1627/jpi.56.69>
  • Adeli Mohsen, Hosainzadegan Hasan, Pakzad Iraj, Zabihi Fatemeh, Alizadeh Maedee, Karimi Fattane: Preparing Starchy Foods Containing Silver Nanoparticles and Evaluating Antimicrobial Activitiy. Jundishapur J Microbiol 2013. <http://dx.doi.org/10.5812/jjm.5075>
  • Tan J., Zhang J. S., Lu Y. C., Xu J. H., Luo G. S.: Process intensification of catalytic hydrogenation of ethylanthraquinone with gas-liquid microdispersion. AlChE Journal 2012, 58, 1326. <http://dx.doi.org/10.1002/aic.12670>
  • Dellavedova Marco, Gigante Lucia, Lunghi Angelo, Pasturenzi Christian, Cardillo Paolo, Salatelli Elisabetta, Zanirato Paolo: Synthesis, Spectroscopic and Thermal Characterization of Azido-1,2,4-triazoles: A Class of Heteroarenes with a High Nitrogen Content. Eur J Org 2012, 2012, 1195. <http://dx.doi.org/10.1002/ejoc.201101450>
  • SURESH KUMAR GANESAN SHUNMUGADHAS, KUMARESAN SUDALAIANDI: Potash alum [KAl(SO 4 ) 2 .12H 2 O] catalysed esterification of formylphenoxyaliphatic acids. J Chem Sci 2012, 124, 857. <http://dx.doi.org/10.1007/s12039-012-0267-8>
  • Tada Kazuya, Onoda Mitsuyoshi: Poor man's green bulk heterojunction photocells: A chlorine-free solvent for poly(3-hexylthiophene)/C60 composites. Sol Energy Mater Sol 2012, 100, 246. <http://dx.doi.org/10.1016/j.solmat.2012.01.026>
  • Li Tingyi, Sun Peng, Yang Hailong, Zhu Yan, Yan Hong, Lu Linhua, Mao Jincheng: Copper-catalyzed decarboxylative coupling of aryl halides with alkynyl carboxylic acids performed in water. Tetrahedron 2012, 68, 6413. <http://dx.doi.org/10.1016/j.tet.2012.06.003>
  • Tan J., Dong C., Lu Y. C., Xu J. H., Luo G. S.: Coupling Process of Oxidation and Extraction in a Gas–Liquid–Liquid Microdispersion System for H2O2 Synthesis. Industrial Eng Chem Res 2012, 51, 1834. <http://dx.doi.org/10.1021/ie2010302>
  • Sachse Alexander, Hulea Vasile, Kostov Krassimir L., Marcotte Nathalie, Boltoeva Maria Yu, Belamie Emmanuel, Alonso Bruno: Efficient mesoporous silica–titania catalysts from colloidal self-assembly. Chem. Commun. 2012, 48, 10648. <http://dx.doi.org/10.1039/c2cc35127g>
  • Gu Yanlong: Multicomponent reactions in unconventional solvents: state of the art. Green Chem. 2012, 14, 2091. <http://dx.doi.org/10.1039/c2gc35635j>
  • Bendicho C., Lavilla I., Pena-Pereira F., Romero V.: Green chemistry in analytical atomic spectrometry: a review. J. Anal. At. Spectrom. 2012, 27, 1831. <http://dx.doi.org/10.1039/c2ja30214d>
  • Sato Bruno M., Martins Clarissa T., El Seoud Omar A.: Solvation in aqueous binary mixtures: consequences of the hydrophobic character of the ionic liquids and the solvatochromic probes. New J. Chem. 2012, 36, 2353. <http://dx.doi.org/10.1039/c2nj40506g>
  • Tada Kazuya, Onoda Mitsuyoshi: Preparation of Bulk Heterojunction Composite Consisting of Poly(3-hexylthiophene) and Neat C$_{70}$ Using Halogen-Free Solvent. Jpn J Appl Phys (Part 1) 2012, 51, 030205. <http://dx.doi.org/10.1143/JJAP.51.030205>
  • Rossi Laura I., Velasco Manuel I.: Alternatives to free molecular halogens as chemoselective reactants: Catalysis of organic reactions with reusable complexes of halogen metal salts. PureAppl Chem 2012, 1. <http://dx.doi.org/10.1351/PAC-CON-11-07-13>
  • Tada Kazuya, Onoda Mitsuyoshi: Preparation of Bulk Heterojunction Composite Consisting of Poly(3-hexylthiophene) and Neat C70Using Halogen-Free Solvent. Jpn. J. Appl. Phys. 2012, 51, 030205. <http://dx.doi.org/10.7567/JJAP.51.030205>
  • Das Subrata, Thakur Ashim Jyoti: A Clean, Highly Efficient and One-Pot Green Synthesis of Aryl/Alkyl/Heteroaryl-Substituted Bis(6-amino-1,3-dimethyluracil-5-yl)methanes in Water. Eur J Org Chem 2011, 2011, 2301. <http://dx.doi.org/10.1002/ejoc.201001581>
  • Nishimi Tomonori, Kamachi Takashi, Kato Kenji, Kato Tomio, Yoshizawa Kazunari: Mechanistic Study on the Production of Hydrogen Peroxide in the Anthraquinone Process. Eur J Org Chem 2011, 2011, 4113. <http://dx.doi.org/10.1002/ejoc.201100300>
  • Dake Satish A., Raut Dnyaneshwar S., Kharat Kiran R., Mhaske Rooth S., Deshmukh Satish U., Pawar Rajendra P.: Ionic liquid promoted synthesis, antibacterial and in vitro antiproliferative activity of novel α-aminophosphonate derivatives. Biorg Med Chem Lett 2011, 21, 2527. <http://dx.doi.org/10.1016/j.bmcl.2011.02.039>
  • Siddiqui Zeba N., Mohammed Musthafa T.N., Ahmad Anis, Khan Asad U.: Thermal solvent-free synthesis of novel pyrazolyl chalcones and pyrazolines as potential antimicrobial agents. Biorg Med Chem Lett 2011, 21, 2860. <http://dx.doi.org/10.1016/j.bmcl.2011.03.080>
  • Luo G.S., Tan J., Du L., Lu Y.C., Xu J.H.: Development of a gas–liquid microstructured system for oxidation of hydrogenated 2-ethyltetrahydroanthraquinone. Chem Eng J 2011, 171, 1406. <http://dx.doi.org/10.1016/j.cej.2011.05.060>
  • Popowycz Florence, Métay Estelle, Lemaire Marc: Direct arylation: Alternative to classic cross-coupling chemistry and a fruitful synthetic tool for the access to novative bioactive molecules. Chim 2011, 14, 621. <http://dx.doi.org/10.1016/j.crci.2010.06.006>
  • Velasco Manuel I., Kinen Claudio O., Hoyos de Rossi Rita, Rossi Laura I.: A green alternative to synthetize azo compounds. J Dye Pig 2011, 90, 259. <http://dx.doi.org/10.1016/j.dyepig.2010.12.009>
  • Zhang Hongming, Lu Jinlong, Wang Xianhong, Li Ji, Wang Fosong: From amorphous to crystalline: Practical way to improve electrical conductivity of water-borne conducting polyaniline. Polymer 2011, 52, 3059. <http://dx.doi.org/10.1016/j.polymer.2011.02.031>
  • Tan J., Liu Z.D., Lu Y.C., Xu J.H., Luo G.S.: Process intensification of H2O2 extraction using gas–liquid–liquid microdispersion system. Separation Purification Technology 2011, 80, 225. <http://dx.doi.org/10.1016/j.seppur.2011.04.030>
  • Hosseini-Sarvari Mona, Sodagar Esmat, Doroodmand Mohammad Mahdi: Nano Sulfated Titania as Solid Acid Catalyst in Direct Synthesis of Fatty Acid Amides. J Org Chem 2011, 76, 2853. <http://dx.doi.org/10.1021/jo2002769>
  • Procopio Antonio, Cravotto Giancarlo, Oliverio Manuela, Costanzo Paola, Nardi Monica, Paonessa Rosina: An eco-sustainable erbium(iii)-catalyzed method for formation/cleavage of O-tert-butoxy carbonates. Green Chem 2011, 13, 436. <http://dx.doi.org/10.1039/c0gc00728e>
  • Gawande Manoj B., Branco Paula S.: An efficient and expeditious Fmoc protection of amines and amino acids in aqueous media. Green Chem 2011, 13, 3355. <http://dx.doi.org/10.1039/c1gc15868f>
  • Belamie Emmanuel, Boltoeva Maria Yu, Yang Ke, Cacciaguerra Thomas, Alonso Bruno: Tunable hierarchical porosity from self-assembled chitin–silica nano-composites. J Materials Chemistry 2011, 21, 16997. <http://dx.doi.org/10.1039/c1jm12110c>
  • Firouzabadi Habib, Iranpoor Nasser, Gholinejad Mohammad, Kazemi Faezeh: Agarose hydrogel as an effective bioorganic ligand and support for the stabilization of palladium nanoparticles. Application as a recyclable catalyst for Suzuki–Miyaura reaction in aqueous media. RSC Adv 2011, 1, 1013. <http://dx.doi.org/10.1039/c1ra00480h>
  • Marjani Katayoun, Khalesi Maryam, Ashouri Akram, Jalali Aazam, Ziyaei-Halimehjani Azim: Catalyst-Free Conjugate Addition of Thioacids to Activated Olefins Accelerated in Water. Synth Comm 2011, 41, 451. <http://dx.doi.org/10.1080/00397911003587515>
  • Mudhoo Ackmez, Forster-Carneiro Tânia, Sánchez Antoni: Biohydrogen production and bioprocess enhancement: A review. Crit Rev Biotechnol 2011, 31, 250. <http://dx.doi.org/10.3109/07388551.2010.525497>
  • Yamada Yoichi M. A., Uozumi Yasuhiro: Development of Polymeric Metal Catalysts via Molecular Convolution and of Catalytic Membrane-Installed Microflow Devices. J Syn Org Chem Jpn 2011, 69, 542. <http://dx.doi.org/10.5059/yukigoseikyokaishi.69.542>
  • Khatik Gopal L., Pal Anang, Apsunde Tushar D., Nair Vipin A.: A highly efficient methodology for 5-methyl-3-aryl-2-thiooxazolidin-4-ones using lithium perchlorate in DIPEA mediated synthesis. J Heterocyclic Chem 2010, n/a. <http://dx.doi.org/10.1002/jhet.369>
  • Gürbüz Nevin, Vural Sema, Yaşar Sedat, Özdemir İsmail, Seçkin Turgay: Pd Functionalized MCM-41 Catalysts for Suzuki Reactions. J Inorg Organomet Polym 2010, 20, 19. <http://dx.doi.org/10.1007/s10904-009-9315-3>
  • Juwarkar Asha A., Singh Sanjeev K., Mudhoo Ackmez: A comprehensive overview of elements in bioremediation. Re/Views in Environmental Science and Bio/Technology 2010, 9, 215. <http://dx.doi.org/10.1007/s11157-010-9215-6>
  • Subramaniam Bala: Gas-expanded liquids for sustainable catalysis and novel materials: Recent advances. Coord Chem Rev - 2010, 254, 1843. <http://dx.doi.org/10.1016/j.ccr.2009.12.009>
  • Serbanovic Ana, Petrovski Željko, Manic Marina, Marques Carolina S., Carrera Gonçalo V.S.M., Branco Luis C., Afonso Carlos A.M., Nunes da Ponte Manuel: Melting behaviour of ionic salts in the presence of high pressure CO2. Fluid Phase Equilb 2010, 294, 121. <http://dx.doi.org/10.1016/j.fluid.2010.03.015>
  • Yip Thomas W. S., Cussen Edmund J., Wilson Claire: Spontaneous formation of crystalline lithium molybdate from solid reagents at room temperature. Dalton Trans 2010, 39, 411. <http://dx.doi.org/10.1039/b908266b>
  • Liu Hongjun, Feng Wei, Kee Choon Wee, Zhao Yujun, Leow Dasheng, Pan Yuanhang, Tan Choon-Hong: Organic dye photocatalyzed α-oxyamination through irradiation with visible light. Green Chem 2010, 12, 953. <http://dx.doi.org/10.1039/b924609f>
  • Coyle Emma E., Joyce Kieran, Nolan Kieran, Oelgemöller Michael: Green photochemistry: the use of microemulsions as green media in photooxygenation reactions. Green Chem 2010, 12, 1544. <http://dx.doi.org/10.1039/c004869k>
  • Al-Zaydi Khadijah M., Nhari Laila M., Borik Rita M., Elnagdi Mohamed H.: Green technologies in organic synthesis: self-condensation of enamines, enaminones and enaminoesters under microwave irradiation in ionic liquid. Green Chem Lett & Revs 2010, 3, 93. <http://dx.doi.org/10.1080/17518250903567261>
  • Mekheimer Ramadan A., Abdelhameed Afaf M., Mohamed Sawsan M., Sadek Kamal Usef: Green, three component highly efficient synthesis of 2-amino-5,6,7,8-tetrahydro-4-H-chromen-3-carbonitriles in water at ambient temperature. Green Chem Lett & Revs 2010, 3, 161. <http://dx.doi.org/10.1080/17518251003619176>
  • Hasaninejad Alireza, Zare Abdolkarim, Mohammadizadeh Mohammad Reza, Shekouhy Mohsen: Lithium bromide as an efficient, green, and inexpensive catalyst for the synthesis of quinoxaline derivatives at room temperature. Green Chem Lett & Revs 2010, 3, 143. <http://dx.doi.org/10.1080/17518251003619192>
  • Rezki N., Sidhoum M. Ait, Aouad M. R., Ilikti H., Benabdallah T.: Pronounced Catalytic Effect of Micellar Solution of Surfactants for Regioselective Alkylation of 4,5-Di- and 3,4,5-Triphenylimidazoles-2-thione. TSD 2010, 47, 376. <http://dx.doi.org/10.3139/113.110089>
  • Firouzabadi Habib, Iranpoor Nasser, Kazemi Somayeh, Ghaderi Arash, Garzan Atefeh: Highly Efficient Halogenation of Organic Compounds with Halides Catalyzed by Cerium(III) Chloride Heptahydrate Using Hydrogen Peroxide as the Terminal Oxidant in Water. Adv Synth Catal 2009, 351, 1925. <http://dx.doi.org/10.1002/adsc.200900124>
  • Liu Qun, Shentu Baoqing, Gu Cheng, Zhu Jinhua, Weng Zhixue: A heterogeneous kinetic model of the oxidative polymerization of 2,6-dimethylphenol with a copper-EDTA complex in water. AIChE 2009, 55, 2716. <http://dx.doi.org/10.1002/aic.11884>
  • Jafari Abbas Ali, Moradgholi Fatemeh, Tamaddon Fatemeh: Pronounced Catalytic Effect of a Micellar Solution of Sodium Dodecylsulfate (SDS) Upon a Three-Component Reaction of Aldehydes, Amines, and Ketones Under Neutral Conditions. Eur J Org Chem 2009, 2009, 1249. <http://dx.doi.org/10.1002/ejoc.200801037>
  • Liu Qun, Shentu Baoqing, Gu Cheng, Weng Zhixue: The initial oxidative polymerization kinetics of 2,6-dimethylphenol with a Cu–EDTA complex in water. Euro Poly J 2009, 45, 1080. <http://dx.doi.org/10.1016/j.eurpolymj.2009.01.012>
  • Firouzabadi Habib, Iranpoor Nasser, Gholinejad Mohammad: 2-Aminophenyl diphenylphosphinite as a new ligand for heterogeneous palladium-catalyzed Heck–Mizoroki reactions in water in the absence of any organic co-solvent. Tetrahedron 2009, 65, 7079. <http://dx.doi.org/10.1016/j.tet.2009.06.081>
  • Elnagdi Mohamed H., Al-Zaydi Khadijah M., Borik Rita M.: Studies with arylhydrazonopyridinones: Synthesis of new arylhydrazono thieno[3,4-c]pyridinones as novel D2T2 dye class; classical verse green methodologies. Ultrasonics Sonochem 2009, 16, 660. <http://dx.doi.org/10.1016/j.ultsonch.2008.11.004>
  • Kinen Claudio Omar, Rossi Laura Isabel, de Rossi Rita Hoyos: The development of an environmentally benign sulfide oxidation procedure and its assessment by green chemistry metrics. Green Chem 2009, 11, 223. <http://dx.doi.org/10.1039/b815986f>
  • Haggiage Elodie, Coyle Emma E., Joyce Kieran, Oelgemöller Michael: Green photochemistry: solarchemical synthesis of 5-amido-1,4-naphthoquinones. Green Chem 2009, 11, 318. <http://dx.doi.org/10.1039/b816676e>
  • Urbani Carl N., Monteiro Michael J.: RAFT-Mediated Emulsion Polymerization of Styrene in Water using a Reactive Polymer Nanoreactor. Aust J Chem 2009, 62, 1528. <http://dx.doi.org/10.1071/CH09222>
  • Firouzabadi H., Iranpoor N., Kazemi S.: Direct halogenation of organic compounds with halides using oxone in water — A green protocol. Can J Chem 2009, 87, 1675. <http://dx.doi.org/10.1139/V09-125>
  • Oe Yohei, Uozumi Yasuhiro: Highly Efficient Heterogeneous Aqueous Kharasch Reaction with an Amphiphilic Resin-Supported Ruthenium Catalyst. Adv Synth Catal 2008, 350, 1771. <http://dx.doi.org/10.1002/adsc.200800359>
  • Donnola Paola, Maggini Michele, Rossetto Massimiliano, Rossi Emiliano, Carofiglio Tommaso: Fullerene-Promoted Singlet-Oxygen Photochemical Oxygenations in Glass-Polymer Microstructured Reactors. Adv Synth Catal 2008, 350, 2815. <http://dx.doi.org/10.1002/adsc.200800459>
  • Kohno Kazufumi, Choi Jun-Chul, Ohshima Yoshihiro, Yasuda Hiroyuki, Sakakura Toshiyasu: Synthesis of Dimethyl Carbonate from Carbon Dioxide Catalyzed by Titanium Alkoxides with Polyether-type Ligands. ChemSusChem 2008, 1, 186. <http://dx.doi.org/10.1002/cssc.200700113>
  • Heinze Thomas, Dorn Susann, Schöbitz Michael, Liebert Tim, Köhler Sarah, Meister Frank: Interactions of Ionic Liquids with Polysaccharides – 2: Cellulose. Macromol Symp 2008, 262, 8. <http://dx.doi.org/10.1002/masy.200850202>
  • Yadav Jhillu S., Reddy Basi V. Subba, Swamy Tallapally, Shankar Kattela Shiva: Green protocol for conjugate addition of amines to p-quinones accelerated by water. Monatshefte für Chemie 2008, 139, 1317. <http://dx.doi.org/10.1007/s00706-008-0917-1>
  • Kamal Ahmed, Reddy J. Surendranadha, Bharathi E. Vijaya, Dastagiri D.: Base-free monosulfonylation of amines using tosyl or mesyl chloride in water. Tetrahetron Lett 2008, 49, 348. <http://dx.doi.org/10.1016/j.tetlet.2007.11.044>
  • 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>
  • Mekheimer Ramadan Ahmed, Hameed Afaf Abdel, Sadek Kamal Usef: Solar thermochemical reactions: four-component synthesis of polyhydroquinoline derivatives induced by solar thermal energy. Green Chem 2008, 10, 592. <http://dx.doi.org/10.1039/b715126h>
  • Chakraborti Asit K., Roy Sudipta Raha, Kumar Dinesh, Chopra Pradeep: Catalytic application of room temperature ionic liquids: [bmim][MeSO4] as a recyclable catalyst for synthesis of bis(indolyl)methanes. Ion-fishing by MALDI-TOF-TOF MS and MS/MS studies to probe the proposed mechanistic model of catalysis. Green Chem 2008, 10, 1111. <http://dx.doi.org/10.1039/b807572g>
  • Palimkar Sanjay S., More Vijaykumar S., Srinivasan Kumar V.: Simple and Efficient One‐Pot, Three‐Component, Solvent‐Free Synthesis of β‐Enaminones via Sonogashira Coupling–Michael Addition Sequences. Synth Comm 2008, 38, 1456. <http://dx.doi.org/10.1080/00397910801914343>
  • Firouzabadi Habib, Iranpoor Nasser, Khoshnood Abbas: Aluminum tris (dodecyl sulfate) trihydrate Al(DS)3·3H2O as an efficient Lewis acid–surfactant-combined catalyst for organic reactions in water. Journal of Molecular Catalysis A 2007, 274, 109. <http://dx.doi.org/10.1016/j.molcata.2007.04.035>
  • Yadav J.S., Swamy T., Reddy B.V. Subba, Rao D. Krishna: Organic synthesis in water: Green protocol for the conjugate addition of thiols to p-quinones. Journal of Molecular Catalysis A 2007, 274, 116. <http://dx.doi.org/10.1016/j.molcata.2007.04.037>
  • Khatik Gopal L., Sharma Gaurav, Kumar Raj, Chakraborti Asit K.: Scope and limitations of HClO4–SiO2 as an extremely efficient, inexpensive, and reusable catalyst for chemoselective carbon–sulfur bond formation. Tetrahedron 2007, 63, 1200. <http://dx.doi.org/10.1016/j.tet.2006.11.050>
  • Ribeiro Sonia M., Serra Arménio C., Rocha Gonsalves A.M.d'A.: Covalently immobilized porphyrins as photooxidation catalysts. Tetrahedron 2007, 63, 7885. <http://dx.doi.org/10.1016/j.tet.2007.05.084>
  • Gaspari Marco, Nardi Monica, Procopio Antonio, Oliverio Manuela, Tagarelli Antonio, Sindona Giovanni: Simple and efficient MW-assisted cleavage of acetals and ketals in pure water. Tetrahetron Lett 2007, 48, 8623. <http://dx.doi.org/10.1016/j.tetlet.2007.10.038>
  • Chakraborti Asit K., Rudrawar Santosh, Jadhav Kirtikumar B., Kaur Gurmeet, Chankeshwara Sunay V.: “On water” organic synthesis: a highly efficient and clean synthesis of 2-aryl/heteroaryl/styryl benzothiazoles and 2-alkyl/aryl alkyl benzothiazolines. Green Chem 2007, 9, 1335. <http://dx.doi.org/10.1039/b710414f>
  • Motiwala Hashim F., Kumar Raj, Chakraborti Asit K.: Microwave-Accelerated Solvent- and Catalyst-Free Synthesis of 4-Aminoaryl/alkyl-7-chloroquinolines and 2-Aminoaryl/alkylbenzothiazoles. Aust J Chem 2007, 60, 369. <http://dx.doi.org/10.1071/CH06391>
  • Houndonougbo Y., Kuczera K., Subramaniam B., Laird B.B.: Prediction of phase equilibria and transport properties in carbon-dioxide expanded solvents by molecular simulation. Mol Simul 2007, 33, 861. <http://dx.doi.org/10.1080/08927020701310923>
  • Firouzabadi H., Iranpoor N., Jafari A. A., Riazymontazer E.: Metal-Free Chemoselective Oxidation of Sulfides to Sulfoxides by Hydrogen Peroxide Catalyzed byin situ Generated Dodecyl Hydrogen Sulfate in the Absence of Organic Co-Solvents. Adv Synth Catal 2006, 348, 434. <http://dx.doi.org/10.1002/adsc.200505312>
  • Rossbach Benjamin M., Leopold Kerstin, Weberskirch Ralf: Selbstorganisierte Nanoreaktoren als hochaktive Katalysatoren in der hydrolytischen Ringöffnung terminaler Epoxide in Wasser. Angew Chem 2006, 118, 1331. <http://dx.doi.org/10.1002/ange.200503291>
  • Rossbach Benjamin M., Leopold Kerstin, Weberskirch Ralf: Self-Assembled Nanoreactors as Highly Active Catalysts in the Hydrolytic Kinetic Resolution (HKR) of Epoxides in Water. Angew Chem Int Ed 2006, 45, 1309. <http://dx.doi.org/10.1002/anie.200503291>
  • Zheng Peng-Wu, Xie Xue-Min, Wang Wei, Wang Xiao-Ji, Guo Yu-Ping, Tu Qi-Dong: Reduction of Azide to Amine Using Fe/AlCl3 or Fe/BiCl3 System in Aqueous EtOH. Chin J Chem 2006, 24, 825. <http://dx.doi.org/10.1002/cjoc.200690157>
  • Fan Xue Sen, Li Yan Zhen, Zhang Xin Ying, Qu Gui Rong, Wang Jian Ji, Hu Xue Yuan: An efficient and green synthesis of 1,4-dihydropyridine derivatives through multi-component reaction in ionic liquid. Heteroatom Chem 2006, 17, 382. <http://dx.doi.org/10.1002/hc.20221>
  • Cheng Chunsheng, Li Zhinian, Shu Jinyan, Li Tao, Zhang Baoyan: Synthesis of isoxazolidines by 1,3-dipolar cycloaddition and their bioactivity. Front. Chem. China 2006, 1, 427. <http://dx.doi.org/10.1007/s11458-006-0068-z>
  • Laska Urszula, Wilk A., Maliszewska Irena, Syper Ludwik: Novel glucose-derived gemini surfactants with a 1,1′-ethylenebisurea spacer: Preparation, thermotropic behavior, and biological properties. J Surfact Deterg 2006, 9, 115. <http://dx.doi.org/10.1007/s11743-006-0380-0>
  • De Rosa Margherita, Lamberti Marina, Pellecchia Claudio, Scettri Arrigo, Villano Rosaria, Soriente Annunziata: An efficient solvent free catalytic oxidation of sulfides to sulfoxides with hydrogen peroxide catalyzed by a binaphthyl-bridged Schiff base titanium complex. Tetrahetron Lett 2006, 47, 7233. <http://dx.doi.org/10.1016/j.tetlet.2006.07.133>
  • Khatik Gopal L., Kumar Raj, Chakraborti Asit K.: Catalyst-Free Conjugated Addition of Thiols to α,β-Unsaturated Carbonyl Compounds in Water. Org Lett 2006, 8, 2433. <http://dx.doi.org/10.1021/ol060846t>
  • Chankeshwara Sunay V., Chakraborti Asit K.: Catalyst-Free Chemoselective N-tert-Butyloxycarbonylation of Amines in Water. Org Lett 2006, 8, 3259. <http://dx.doi.org/10.1021/ol0611191>
  • Sjöström Jesper: Green chemistry in perspective—models for GC activities and GC policy and knowledge areas. Green Chem 2006, 8, 130. <http://dx.doi.org/10.1039/b511316d>
  • Chakraborti Asit K., Chankeshwara Sunay V.: HClO4?SiO2 as a new, highly efficient, inexpensive and reusable catalyst for N-tert-butoxycarbonylation of amines. Org Biomol Chem 2006, 4, 2769. <http://dx.doi.org/10.1039/b605074c>
  • Oelgem?ller Michael, Healy Niall, de Oliveira Lamark, Jung Christian, Mattay Jochen: Green photochemistry: solar-chemical synthesis of Juglone with medium concentrated sunlight. Green Chem 2006, 8, 831. <http://dx.doi.org/10.1039/b605906f>
  • Firouzabadi H., Iranpoor N., Jafari A. A.: Micellar Solution of Sodium Dodecyl Sulfate (SDS) Catalyzes Facile Michael Addition of Amines and Thiols to α,β-Unsaturated Ketones in Water under Neutral Conditions. Adv Synth Catal 2005, 347, 655. <http://dx.doi.org/10.1002/adsc.200404348>
  • Firouzabadi Habib, Iranpoor Nasser, Garzan Atefeh: Pronounced Catalytic Effect of Micellar Solution of Sodium Dodecyl Sulfate (SDS) for Regioselective Iodination of Aromatic Compounds with a Sodium Iodide/Cerium(IV) Trihydroxide Hydroperoxide System. Adv Synth Catal 2005, 347, 1925. <http://dx.doi.org/10.1002/adsc.200505222>
  • Schönfelder Daniel, Nuyken Oskar, Weberskirch Ralf: Heck and Suzuki coupling reactions in water using poly(2-oxazoline)s functionalized with palladium carbene complexes as soluble, amphiphilic polymer supports. J Organomet Chem 2005, 690, 4648. <http://dx.doi.org/10.1016/j.jorganchem.2005.07.053>
  • Wang Q.G., Wang X.H., Li J., Zhao X.J., Wang F.S.: Water-borne conductive polyaniline doped by acidic phosphate ester containing polysilsesquioxane precursor. Synthetic Metal 2005, 148, 127. <http://dx.doi.org/10.1016/j.synthmet.2004.09.025>
  • Shen Zhen Lu, Jiang Xuan Zhen, Mo Wei Min, Hu Bao Xiang, Sun Nan: Catalytic O-methylation of phenols with dimethyl carbonate to aryl methyl ethers using [BMIm]Cl. Green Chem 2005, 7, 97. <http://dx.doi.org/10.1039/b411201f>
  • Procopio Antonio, Dalpozzo Renato, De Nino Antonio, Maiuolo Loredana, Nardi Monica, Romeo Giovanni: Mild and efficient method for the cleavage of benzylidene acetals by using erbium (iii) triflate. Org Biomol Chem 2005, 3, 4129. <http://dx.doi.org/10.1039/b511314h>
  • Yamada Yoichi M. A.: Self-Assembled Complexes of Non-cross-linked Amphiphilic Polymeric Ligands with Inorganic Species: Highly Active and Reusable Solid-Phase Polymeric Catalysts. Chem Pharm Bull 2005, 53, 723. <http://dx.doi.org/10.1248/cpb.53.723>
  • YAMADA Yoichi M. A.: Development of Novel Solid-phase Polymeric Catalysts for Organic Syntheses. YAKUGAKU ZASSHI 2005, 125, 749. <http://dx.doi.org/10.1248/yakushi.125.749>
  • Procopio Antonio, Dalpozzo Renato, De Nino Antonio, Maiuolo Loredana, Russo Beatrice, Sindona Giovanni: Erbium(III) Triflate as an Extremely Active Acylation Catalyst. Adv Synth Catal 2004, 346, 1465. <http://dx.doi.org/10.1002/adsc.200404132>
  • 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>
  • Shen Zhen Lu, Jiang Xuan Zhen: Selective N,N-dimethylation of primary aromatic amines with dimethyl carbonate in the presence of diphenylammonium triflate. Journal of Molecular Catalysis A 2004, 213, 193. <http://dx.doi.org/10.1016/j.molcata.2003.12.008>
  • Paul Satya, Clark James H.: Structure-activity relationship between some novel silica supported palladium catalysts: a study of the Suzuki reaction. Journal of Molecular Catalysis A 2004, 215, 107. <http://dx.doi.org/10.1016/j.molcata.2003.12.034>
  • Nameroff T.J, Garant R.J, Albert M.B: Adoption of green chemistry: an analysis based on US patents. Policy Research 2004, 33, 959. <http://dx.doi.org/10.1016/j.respol.2004.03.001>
  • Yamada Yoichi M.A, Takeda Koji, Takahashi Hideyo, Ikegami Shiro: Assembled catalyst of palladium and non-cross-linked amphiphilic polymer ligand for the efficient heterogeneous Heck reaction. Tetrahedron 2004, 60, 4097. <http://dx.doi.org/10.1016/j.tet.2004.02.068>
  • Yamada Yoichi M.A, Tabata Hidetsugu, Ichinohe Masato, Takahashi Hideyo, Ikegami Shiro: Oxidation of allylic alcohols, amines, and sulfides mediated by assembled triphase catalyst of phosphotungstate and non-cross-linked amphiphilic copolymer. Tetrahedron 2004, 60, 4087. <http://dx.doi.org/10.1016/j.tet.2004.02.072>
  • Toyota Masahiro, Ilangovan Andivelu, Kashiwagi Yoshitomo, Ihara Masataka: One-Pot Assembly of Tricyclo[6.2.1.01,6]undecan-4-one and Related Polycyclic Compounds by Tandem Electroreductive Cyclization. Org Lett 2004, 6, 3629. <http://dx.doi.org/10.1021/ol0484660>
  • Vasapollo Giuseppe, Mele Giuseppe, Maffei Annamaria, Sole Roberta Del: Palladium-catalysed cyclocarbonylation reactions in dimethyl carbonate, an eco-friendly solvent and ring-opening reagent. Appl Organometal Chem 2003, 17, 835. <http://dx.doi.org/10.1002/aoc.543>
  • Yamada Yoichi M.A, Takeda Koji, Takahashi Hideyo, Ikegami Shiro: An efficient heterogeneous Heck reaction promoted by a new assembled catalyst of palladium and non-cross-linked amphiphilic polymer. Tetrahetron Lett 2003, 44, 2379. <http://dx.doi.org/10.1016/S0040-4039(03)00220-X>
  • Centi Gabriele, Perathoner Siglinda: Catalysis and sustainable (green) chemistry. Catal Today 2003, 77, 287. <http://dx.doi.org/10.1016/S0920-5861(02)00374-7>
  • Ouk Samedy, Thiébaud Sophie, Borredon Elisabeth, Le Gars Pierre: High performance method for O-methylation of phenol with dimethyl carbonate. CATAL A GENERAL 2003, 241, 227. <http://dx.doi.org/10.1016/S0926-860X(02)00467-2>
  • Airoldi Claudio, Prado Alexandre G.S.: The inhibitory biodegradation effects of the pesticide 2,4-D when chemically anchored on silica gel. Thermochimica 2002, 394, 163. <http://dx.doi.org/10.1016/S0040-6031(02)00266-6>
  • LeStrat Franck, Murphy John A., Hughes Mark: Direct Electroreductive Preparation of Indolines and Indoles from Diazonium Salts. Org Lett 2002, 4, 2735. <http://dx.doi.org/10.1021/ol0262643>
  • Yamada Yoichi M. A., Takeda Koji, Takahashi Hideyo, Ikegami Shiro: An Assembled Complex of Palladium and Non-Cross-linked Amphiphilic Polymer:  A Highly Active and Recyclable Catalyst for the Suzuki−Miyaura Reaction. Org Lett 2002, 4, 3371. <http://dx.doi.org/10.1021/ol0264612>
  • Strukul Giorgio: Chemistry: How green was my ester. Nature 2001, 412, 388. <http://dx.doi.org/10.1038/35086670>
  • Roon André van, Govers Harrie A.J., R. John, Weenen Hans van: Sustainable chemistry: an analysis of the concept and its integration in education. Int J Sustainability in HE 2001, 2, 161. <http://dx.doi.org/10.1108/14676370110388372>