Pure and Applied Chemistry

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• Talbot Eric P. A., Richardson Melodie, McKenna Jeffrey M., Toste F. Dean: Gold-Catalyzed Redox Synthesis of Imidazo[1,2-a ]pyridines using Pyridine N -Oxide and Alkynes. Adv. Synth. Catal. 2014, 356, 687. <http://dx.doi.org/10.1002/adsc.201300996>
• Vega-Peñaloza Alberto, Sánchez-Antonio Omar, Ávila-Ortiz C. Gabriela, Escudero-Casao Margarita, Juaristi Eusebio: An Alternative Synthesis of Chiral (S )-Proline Derivatives that Contain a Thiohydantoin Moiety and Their Application as Organocatalysts in the Asymmetric Michael Addition Reaction under Solvent-Free Conditions. Asian Journal of Organic Chemistry 2014, n/a. <http://dx.doi.org/10.1002/ajoc.201400018>
• Sawadjoon Supaporn, Sjöberg Per J. R., Orthaber Andreas, Matsson Olle, Samec Joseph S. M.: Mechanistic Insights into the Pd-Catalyzed Direct Amination of Allyl Alcohols: Evidence for an Outer-Sphere Mechanism Involving a Palladium Hydride Intermediate. Chem. Eur. J. 2014, 20, 1520. <http://dx.doi.org/10.1002/chem.201303431>
• Dubé Marc A., Salehpour Somaieh: Applying the Principles of Green Chemistry to Polymer Production Technology. Macromol. React. Eng. 2014, 8, 7. <http://dx.doi.org/10.1002/mren.201300103>
• Mirjafari Arsalan: Direct synthesis of 2,4,5-trisubstituted imidazoles from alcohols and α-hydroxyketones by microwave. Environ Chem Lett 2014, 12, 177. <http://dx.doi.org/10.1007/s10311-013-0423-5>
• Joshi Vijaykumar M., Magar Rupali L., Throat Prashant B., Tekale Sunil U., Patil Bhagavan R., Kale Mangal P., Pawar Rajendra P.: Novel one-pot synthesis of 4H-chromene derivatives using amino functionalized silica gel catalyst. Chinese Chemical Letters 2014, 25, 455. <http://dx.doi.org/10.1016/j.cclet.2013.12.016>
• Wang Yu, Su Na, Ye Lin, Ren Yuanhang, Chen Xueying, Du Yujue, Li Zhenhua, Yue Bin, Tsang Shik Chi Edman, Chen Qiao, He Heyong: Tuning enantioselectivity in asymmetric hydrogenation of acetophenone and its derivatives via confinement effect over free-standing mesoporous palladium network catalysts. Journal of Catalysis 2014, 313, 113. <http://dx.doi.org/10.1016/j.jcat.2014.03.004>
• Homma Taichi, Kitaoka Takuya: Preparation of porous paper composites with ruthenium hydroxide and catalytic alcohol oxidation in a multiphase gas–liquid–solid reaction. Materials Science and Engineering: B 2014, 184, 7. <http://dx.doi.org/10.1016/j.mseb.2014.01.011>
• Wang Wei, Zhao Xue-Mei, Wang Jing-Li, Geng Xin, Gong Jun-Fang, Hao Xin-Qi, Song Mao-Ping: Transition metal-free synthesis of primary amides from aldehydes and hydroxylamine hydrochloride. Tetrahedron Letters 2014. <http://dx.doi.org/10.1016/j.tetlet.2014.04.020>
• Sharma Manu, Das Debashree, Baruah Arabinda, Jain Archana, Ganguli Ashok K.: Design of Porous Silica Supported Tantalum Oxide Hollow Spheres Showing Enhanced Photocatalytic Activity. Langmuir 2014, 30, 3199. <http://dx.doi.org/10.1021/la500167a>
• Sawadjoon Supaporn, Orthaber Andreas, Sjöberg Per J. R., Eriksson Lars, Samec Joseph S. M.: Equilibrium Study of Pd(dba)2 and P(OPh)3 in the Pd-Catalyzed Allylation of Aniline by Allyl Alcohol. Organometallics 2014, 33, 249. <http://dx.doi.org/10.1021/om4009873>
• Brahmachari Goutam, Banerjee Bubun: Facile and One-Pot Access to Diverse and Densely Functionalized 2-Amino-3-cyano-4H-pyrans and Pyran-Annulated Heterocyclic Scaffolds via an Eco-Friendly Multicomponent Reaction at Room Temperature Using Urea as a Novel Organo-Catalyst. ACS Sustainable Chem. Eng. 2014, 2, 411. <http://dx.doi.org/10.1021/sc400312n>
• Toniolo Sara, Aricò Fabio, Tundo Pietro: A Comparative Environmental Assessment for the Synthesis of 1,3-Oxazin-2-one by Metrics: Greenness Evaluation and Blind Spots. ACS Sustainable Chem. Eng. 2014, 2, 1056. <http://dx.doi.org/10.1021/sc500070t>
• Schulz Tim, Färber Christian, Leibold Michael, Bruhn Clemens, Prochnow Pascal, Bandow Julia E., Schneider Tanja, Porsch Timo, Holthausen Max C., Siemeling Ulrich: Diastereoselective synthesis of a bicyclic β-lactam with penicillin G-like spectrum of activity by carbonylation of an acyclic diaminocarbene. Chem. Commun. 2014, 50, 2341. <http://dx.doi.org/10.1039/c3cc48538b>
• Sheldon Roger A.: Green and sustainable manufacture of chemicals from biomass: state of the art. Green Chem. 2014, 16, 950. <http://dx.doi.org/10.1039/c3gc41935e>
• Ghavre Mukund, Byrne Owen, Altes Lena, Surolia Praveen K., Spulak Marcel, Quilty Brid, Thampi K. Ravindranathan, Gathergood Nicholas: Low toxicity functionalised imidazolium salts for task specific ionic liquid electrolytes in dye-sensitised solar cells: a step towards less hazardous energy production. Green Chem. 2014, 16, 2252. <http://dx.doi.org/10.1039/c3gc42393j>
• Brahmachari Goutam, Das Suvankar: l-Proline catalyzed multicomponent one-pot synthesis of gem-diheteroarylmethane derivatives using facile grinding operation under solvent-free conditions at room temperature. RSC Adv. 2014, 4, 7380. <http://dx.doi.org/10.1039/c3ra44568b>
• Lal Samridhi, Snape Timothy J.: Towards a sustainable synthesis of aniline-derived amides using an indirect chemoenzymatic process: challenges and successes. RSC Adv. 2014, 4, 1609. <http://dx.doi.org/10.1039/c3ra46499g>
• Mahindra Amit, Patel Neha, Bagra Nitin, Jain Rahul: Solvent-free peptide synthesis assisted by microwave irradiation: environmentally benign synthesis of bioactive peptides. RSC Adv. 2014, 4, 3065. <http://dx.doi.org/10.1039/c3ra46643d>
• Tsuji Yasushi: Transition Metal-Catalyzed Synthesis of π-Conjugated Cyclic Ester and Amides from Alkynes and Carbonyl Reagents. HETEROCYCLES 2014, 89. <http://dx.doi.org/10.3987/REV-13-786>
• Khan Imran A., Saxena Anil K.: ( R/S )-BINOL-α-Phosphoryloxy Enecarbamate-Mediated and ( R / S )-Titanium(IV) BINOLates-Catalyzed Enantioselective Intramolecular Heck/Aza-Diels-Alder Cycloaddition (IHADA): An Expedient Methodology. Adv. Synth. Catal. 2013, n/a. <http://dx.doi.org/10.1002/adsc.201300522>
• Schaper Lars-Arne, Hock Sebastian J., Herrmann Wolfgang A., Kühn Fritz E.: Synthese und Anwendung wasserlöslicher NHC-Übergangsmetall-Komplexe. Angew. Chem. 2013, 125, 284. <http://dx.doi.org/10.1002/ange.201205119>
• Schaper Lars-Arne, Hock Sebastian J., Herrmann Wolfgang A., Kühn Fritz E.: Synthesis and Application of Water-Soluble NHC Transition-Metal Complexes. Angew. Chem. Int. Ed. 2013, 52, 270. <http://dx.doi.org/10.1002/anie.201205119>
• Chen Long, Shi Tao-Da, Zhou Jian: Waste as Catalyst: Tandem Wittig/Conjugate Reduction Sequence to α-CF3 γ-Keto Esters That Uses Ph3 PO as Catalyst for the Chemoselective Conjugate Reduction. Chem. Asian J. 2013, 8, 556. <http://dx.doi.org/10.1002/asia.201201130>
• Biswas Srijit, Samec Joseph S. M.: The Efficiency of the Metal Catalysts in the Nucleophilic Substitution of Alcohols is Dependent on the Nucleophile and Not on the Electrophile. Chem. Asian J. 2013, 8, 974. <http://dx.doi.org/10.1002/asia.201201178>
• Chahdoura Faouzi, Dubrulle Laurent, Fourmy Kevin, Durand Jérôme, Madec David, Gómez Montserrat: Glycerol - A Non-Innocent Solvent for Rh-Catalysed Pauson-Khand Carbocyclisations. Eur. J. Inorg. Chem. 2013, 2013, 5138. <http://dx.doi.org/10.1002/ejic.201300651>
• Lee Chia-Hsin, Hsu Wei-Shun, Chen Chih-Hau, Sun Chung-Ming: A Telescoping Synthesis of Chimeric Polyheterocycles through a Piperidine-Mediated Multicomponent Reaction. Eur. J. Org. Chem. 2013, 2013, 2201. <http://dx.doi.org/10.1002/ejoc.201201645>
• Siddiqui I. R., Kumar Devesh, Shamim Shayna: Ionic Liquid Promoted Multicomponent Reaction: A Good Strategy for the Eco-Compatible Synthesis of Functionalized Pyrroles. J. Heterocyclic Chem. 2013, 50, E111. <http://dx.doi.org/10.1002/jhet.1085>
• Liguori Francesca, Barbaro Pierluigi, Giordano Cristiana, Sawa Haruo: Partial hydrogenation reactions over Pd-containing hybrid inorganic/polymeric catalytic membranes. Applied Catalysis A: General 2013, 459, 81. <http://dx.doi.org/10.1016/j.apcata.2013.03.040>
• Habibi Davood, Nasrollahzadeh Mahmoud: An ultrasound-promoted green approach for the N-formylation of amines under solvent- and catalyst-free conditions at room temperature. Comptes Rendus Chimie 2013, 16, 1008. <http://dx.doi.org/10.1016/j.crci.2013.02.020>
• Mobinikhaledi Akbar, Moghanian Hassan, Deinavizadeh Maryam: pTSA-catalyzed condensation of xylenols and aldehydes under solvent-free conditions: One-pot synthesis of 9H-xanthene or bisphenol derivatives. Comptes Rendus Chimie 2013, 16, 1035. <http://dx.doi.org/10.1016/j.crci.2013.03.008>
• Krishnan Gopalakrishnapanicker Rajesh, Sreeraj Modiyuzhathil K., Sreekumar Krishnapillai: Modification of poly(vinyl chloride) with pendant metal complex for catalytic applications. Comptes Rendus Chimie 2013, 16, 736. <http://dx.doi.org/10.1016/j.crci.2013.03.013>
• Zhang Dong-Yang, Zu Yuan-Gang, Fu Yu-Jie, Luo Meng, Wang Wei, Gu Cheng-Bo, Yao Xiao-Hui: Application of immobilized enzymes to accelerate the conversion of genistin to genistein in pigeon pea root extracts and the evaluation their antioxidant activity. Industrial Crops and Products 2013, 42, 409. <http://dx.doi.org/10.1016/j.indcrop.2012.05.039>
• Schulz Tobias, Strassner Thomas: Biphasic platinum catalyzed hydrosilylation of terminal alkenes in TAAILs. Journal of Organometallic Chemistry 2013, 744, 113. <http://dx.doi.org/10.1016/j.jorganchem.2013.05.039>
• Charpenay Mélanie, Boudhar Aicha, Hulot Catherine, Blond Gaëlle, Suffert Jean: Expeditious cascade reactions: controlled syntheses of fenestradienes and cyclooctatrienes under palladium catalysis. Tetrahedron 2013, 69, 7568. <http://dx.doi.org/10.1016/j.tet.2013.05.089>
• Wender Paul A.: Toward the ideal synthesis and transformative therapies: the roles of step economy and function oriented synthesis. Tetrahedron 2013, 69, 7529. <http://dx.doi.org/10.1016/j.tet.2013.06.004>
• Lee Byeongno, Kang Philjun, Lee Kyu Hyung, Cho Jaeheung, Nam Wonwoo, Lee Won Koo, Hur Nam Hwi: Solid-state and solvent-free synthesis of azines, pyrazoles, and pyridazinones using solid hydrazine. Tetrahedron Letters 2013, 54, 1384. <http://dx.doi.org/10.1016/j.tetlet.2012.12.106>
• Sawadjoon Supaporn, Lundstedt Anna, Samec Joseph S. M.: Pd-Catalyzed Transfer Hydrogenolysis of Primary, Secondary, and Tertiary Benzylic Alcohols by Formic Acid: A Mechanistic Study. ACS Catal. 2013, 3, 635. <http://dx.doi.org/10.1021/cs300785r>
• Hamilton Alaina E., Buxton Audrey M., Peeples Christopher J., Chalker Justin M.: An Operationally Simple Aqueous Suzuki–Miyaura Cross-Coupling Reaction for an Undergraduate Organic Chemistry Laboratory. J. Chem. Educ. 2013, 90, 1509. <http://dx.doi.org/10.1021/ed4002333>
• García-Álvarez Joaquín, Díez Josefina, Vidal Cristian, Vicent Cristian: New Ag(I)–Iminophosphorane Coordination Polymers as Efficient Catalysts Precursors for the MW-Assisted Meyer–Schuster Rearrangement of Propargylic Alcohols in Water. Inorg. Chem. 2013, 52, 6533. <http://dx.doi.org/10.1021/ic400511d>
• Motiwala Hashim F., Fehl Charlie, Li Sze-Wan, Hirt Erin, Porubsky Patrick, Aubé Jeffrey: Overcoming Product Inhibition in Catalysis of the Intramolecular Schmidt Reaction. J. Am. Chem. Soc. 2013, 135, 9000. <http://dx.doi.org/10.1021/ja402848c>
• Suzuki Ken, Watanabe Tomonari, Murahashi Shun-Ichi: Oxidation of Primary Amines to Oximes with Molecular Oxygen using 1,1-Diphenyl-2-picrylhydrazyl and WO3/Al2O3 as Catalysts. J. Org. Chem. 2013, 78, 2301. <http://dx.doi.org/10.1021/jo302262a>
• Bai Liangjiu, Zhang Lifen, Pan Jinlong, Zhu Jian, Cheng Zhenping, Zhu Xiulin: Developing a Synthetic Approach with Thermoregulated Phase-Transfer Catalysis: Facile Access to Metal-Mediated Living Radical Polymerization of Methyl Methacrylate in Aqueous/Organic Biphasic System. Macromolecules 2013, 46, 2060. <http://dx.doi.org/10.1021/ma4000489>
• Ganushevich Yulia S., Miluykov Vasily A., Polyancev Fedor M., Latypov Shamil K., Lönnecke Peter, Hey-Hawkins Evamarie, Yakhvarov Dmitry G., Sinyashin Oleg G.: Nickel Phosphanido Hydride Complex: An Intermediate in the Hydrophosphination of Unactivated Alkenes by Primary Phosphine. Organometallics 2013, 32, 3914. <http://dx.doi.org/10.1021/om400408e>
• Konnert Laure, Gauliard Anne, Lamaty Frédéric, Martinez Jean, Colacino Evelina: Solventless Synthesis of N-Protected Amino Acids in a Ball Mill. ACS Sustainable Chem. Eng. 2013, 1, 1186. <http://dx.doi.org/10.1021/sc4001115>
• Yoshida Jun-ichi, Takahashi Yusuke, Nagaki Aiichiro: Flash chemistry: flow chemistry that cannot be done in batch. Chem. Commun. 2013, 49, 9896. <http://dx.doi.org/10.1039/c3cc44709j>
• Bratko Ielyzaveta, Gómez Montserrat: Polymetallic complexes linked to a single-frame ligand: cooperative effects in catalysis. Dalton Trans. 2013, 42, 10664. <http://dx.doi.org/10.1039/c3dt50963j>
• Renault Stéven, Gottis Sébastien, Barrès Anne-Lise, Courty Matthieu, Chauvet Olivier, Dolhem Franck, Poizot Philippe: A green Li–organic battery working as a fuel cell in case of emergency. Energy Environ. Sci. 2013, 6, 2124. <http://dx.doi.org/10.1039/c3ee40878g>
• Borghèse Sophie, Drouhin Pauline, Bénéteau Valérie, Louis Benoit, Pale Patrick: Silver-zeolite catalysed solvent free synthesis of (spiro)ketals. Green Chem. 2013, 15, 1496. <http://dx.doi.org/10.1039/c3gc40422f>
• Vabre Boris, Lindeperg Fabien, Zargarian Davit: Direct, one-pot synthesis of POCOP-type pincer complexes from metallic nickel. Green Chem. 2013, 15, 3188. <http://dx.doi.org/10.1039/c3gc40968f>
• Takahashi Yusuke, Mitsudome Takato, Mizugaki Tomoo, Jitsukawa Koichiro, Kaneda Kiyotomi: Highly atom-efficient and chemoselective reduction of ketones in the presence of aldehydes using heterogeneous catalysts. Green Chem. 2013, 15, 2695. <http://dx.doi.org/10.1039/c3gc41322e>
• Kubička David, Kubičková Iva, Čejka Jiří: Application of Molecular Sieves in Transformations of Biomass and Biomass-Derived Feedstocks. Catalysis Reviews 2013, 55, 1. <http://dx.doi.org/10.1080/01614940.2012.685811>
• Clark James H, Farmer Thomas J, Macquarrie Duncan J, Sherwood James: Using metrics and sustainability considerations to evaluate the use of bio-based and non-renewable Brønsted acidic ionic liquids to catalyse Fischer esterification reactions. Sustain Chem Process 2013, 1, 23. <http://dx.doi.org/10.1186/2043-7129-1-23>
• Yang Jian, Liu Xin, Meng Da-Li, Chen Hong-Yan, Zong Zhi-Hui, Feng Ting-Ting, Sun Kai: Efficient Iron-Catalyzed Direct β-Alkylation of Secondary Alcohols with Primary Alcohols. Synth Catal 2012, 354, 328. <http://dx.doi.org/10.1002/adsc.201000907>
• Trentin Francesco, Chapman Andrew M., Scarso Alessandro, Sgarbossa Paolo, Michelin Rino A., Strukul Giorgio, Wass Duncan F.: Platinum(II) Diphosphinamine Complexes for the Efficient Hydration of Alkynes in Micellar Media. Synth Catal 2012, 354, 1095. <http://dx.doi.org/10.1002/adsc.201100326>
• Seashore-Ludlow Brinton, Danielsson Jakob, Somfai Peter: Domino Carbopalladation-Carbonylation: Investigation of Substrate Scope. Adv. Synth. Catal. 2012, 354, 205. <http://dx.doi.org/10.1002/adsc.201100678>
• Zhou Feng, Cao Zhong-Yan, Zhang Jing, Yang Hai-Bo, Zhou Jian: A Highly Efficient Friedel-Crafts Reaction of 3-Hydroxyoxindoles and Aromatic Compounds to 3,3-Diaryl and 3-Alkyl-3-aryloxindoles Catalyzed by Hg(ClO4)2⋅3 H2O. Chem —Asian J 2012, 7, 233. <http://dx.doi.org/10.1002/asia.201100773>
• Chen Long, Zhou Jian: A Highly Efficient Friedel-Crafts Reaction of Tertiary α-Hydroxyesters or α-Hydroxyketones to α-Quaternary Esters or Ketones. Chem. Asian J. 2012, 7, 2510. <http://dx.doi.org/10.1002/asia.201200693>
• Antiñolo Antonio, Carrillo-Hermosilla Fernando, Cadierno Victorio, García-Álvarez Joaquín, Otero Antonio: Microwave-Assisted Meyer-Schuster Rearrangement of Propargylic Alcohols Catalyzed by the Oxovanadate Complex [V(O)Cl(OEt)2]. ChemCatChem 2012, 4, 123. <http://dx.doi.org/10.1002/cctc.201100239>
• Ranu Brindaban C., Dey Raju, Chatterjee Tanmay, Ahammed Sabir: Copper Nanoparticle-Catalyzed CarbonCarbon and CarbonHeteroatom Bond Formation with a Greener Perspective. ChemSusChem 2012, 5, 22. <http://dx.doi.org/10.1002/cssc.201100348>
• Wei Yingxu, Yuan Cuiyu, Li Jinzhe, Xu Shutao, Zhou You, Chen Jingrun, Wang Quanyi, Xu Lei, Qi Yue, Zhang Qing: Coke Formation and Carbon Atom Economy of Methanol-to-Olefins Reaction. ChemSusChem 2012, 5, 906. <http://dx.doi.org/10.1002/cssc.201100528>
• Khan Farooq-Ahmad, Süss-Fink Georg: Superparamagnetic Core-Shell-Type Fe3O4/Ru Nanoparticles as Catalysts for the Selective Hydrogenation of an Unconstrained α,β-Unsaturated Ketone. Euro J Inorg Chem 2012, 2012, 727. <http://dx.doi.org/10.1002/ejic.201100869>
• Barbaro Pierluigi, Liguori Francesca, Linares Noemi, Marrodan Carmen Moreno: Heterogeneous Bifunctional Metal/Acid Catalysts for Selective Chemical Processes. Eur. J. Inorg. Chem. 2012, 2012, 3807. <http://dx.doi.org/10.1002/ejic.201200529>
• García-Álvarez Joaquín, Díez Josefina, Gimeno Jose, Suárez Francisco J., Vincent Cristian: (Iminophosphorane)copper(I) Complexes as Highly Efficient Catalysts for 1,3-Dipolar Cycloaddition of Azides with Terminal and 1-Iodoalkynes in Water: One-Pot Multi-Component Reaction from Alkynes and in situ Generated Azides. Eur. J. Inorg. Chem. 2012, 2012, 5854. <http://dx.doi.org/10.1002/ejic.201200789>
• Krupková Alena, Čermák Jan: Carbosilane Metallodendrimers with Cyclopentadienyldichlorotitanium(IV) End Groups. J Inorg Organomet Polym 2012, 22, 470. <http://dx.doi.org/10.1007/s10904-011-9632-1>
• Wei Yen, Das Sudipto, Berke-Schlessel David, Ji Hai-Feng, McDonough John, Feng Lin, Zhang Xiang, Zhai Wentao, Cao Yingze: Synthesis of a Re-usable Cellobiase Enzyme Catalyst through In situ Encapsulation in Nonsurfactant Templated Sol–Gel Mesoporous Silica. Top Catal 2012, 55, 1247. <http://dx.doi.org/10.1007/s11244-012-9892-1>
• López-Garzón Camilo S., Ottens Marcel, van der Wielen Luuk A.M., Straathof Adrie J.J.: Direct downstream catalysis: From succinate to its diethyl ester without intermediate acidification. Chemical Engineering Journal 2012, 200-202, 637. <http://dx.doi.org/10.1016/j.cej.2012.06.079>
• Aghapoor Kioumars, Mohsenzadeh Farshid, Mohebi Morad Mina, Darabi Hossein Reza: Sustainable approach to tandem catalysis: Expedient access to quinoxalines and pyrido[2,3-b]pyrazines from α-hydroxyketones via microwave-induced [(NH4)6Mo7O24·4H2O – PEG 300] polar paste catalyst system. Comptes Rendus Chimie 2012, 15, 764. <http://dx.doi.org/10.1016/j.crci.2012.06.007>
• Fu Zhiyong, Tan Yi, Zhang Jie, Liao Shijun, Su Dongpo, Chen Hengjun, Yu Yue, Peng Junjie: An efficient basic catalyst based on a new germanium coordination complex. J Inorg Chem Commun 2012, 15, 221. <http://dx.doi.org/10.1016/j.inoche.2011.10.031>
• Lal Samridhi, Snape Timothy J.: Exploitation of a Candida antarctica lipase B-catalysed in situ carboxylic acid activation method for the synthesis of acetanilides. Journal of Molecular Catalysis B: Enzymatic 2012, 83, 80. <http://dx.doi.org/10.1016/j.molcatb.2012.07.007>
• Lazny Ryszard, Ratkiewicz Artur, Nodzewska Aneta, Wysocka Joanna: A DFT study of the origins of the stereoselectivity in the aldol reaction of bicyclic amino ketones in the presence of water. Tetrahedron Letters 2012, 53, 5871. <http://dx.doi.org/10.1016/j.tetlet.2012.08.070>
• Iwai Tomohiro, Fujihara Tetsuaki, Terao Jun, Tsuji Yasushi: Iridium-Catalyzed Addition of Aroyl Chlorides and Aliphatic Acid Chlorides to Terminal Alkynes. J. Am. Chem. Soc. 2012, 134, 1268. <http://dx.doi.org/10.1021/ja209679c>
• Ananikov Valentine P., Orlov Nikolay V., Zalesskiy Sergey S., Beletskaya Irina P., Khrustalev Victor N., Morokuma Keiji, Musaev Djamaladdin G.: Catalytic Adaptive Recognition of Thiol (SH) and Selenol (SeH) Groups Toward Synthesis of Functionalized Vinyl Monomers. S J Am Chem Soc 2012, 134, 6637. <http://dx.doi.org/10.1021/ja210596w>
• Seashore-Ludlow Brinton, Somfai Peter: Domino Carbopalladation–Cross-Coupling for the Synthesis of 3,3-Disubstituted Oxindoles. Org. Lett. 2012, 14, 3858. <http://dx.doi.org/10.1021/ol301539p>
• Seashore-Ludlow Brinton, Saint-Dizier François, Somfai Peter: Asymmetric Transfer Hydrogenation Coupled with Dynamic Kinetic Resolution in Water: Synthesis of anti-β-Hydroxy-α-amino Acid Derivatives. Org. Lett. 2012, 14, 6334. <http://dx.doi.org/10.1021/ol303115v>
• Azath Ismail Abulkalam, Puthiaraj Pillaiyar, Pitchumani Kasi: One-Pot Multicomponent Solvent-Free Synthesis of 2-Amino-4H-benzo[b]pyrans Catalyzed by Per-6-amino-β-cyclodextrin. ACS Sustainable Chem. Eng. 2012, 121220121753000. <http://dx.doi.org/10.1021/sc3000866>
• Sheldon Roger A.: Fundamentals of green chemistry: efficiency in reaction design. Chemical Society Review 2012, 41, 1437. <http://dx.doi.org/10.1039/c1cs15219j>
• Wiles Charlotte, Watts Paul: Continuous flow reactors: a perspective. Green Chem 2012, 14, 38. <http://dx.doi.org/10.1039/c1gc16022b>
• Biswas Srijit, Samec Joseph S. M.: A gold(i)-catalyzed route to α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols. Chem. Commun. 2012, 48, 6586. <http://dx.doi.org/10.1039/c2cc32042h>
• Ohshima Takashi, Hayashi Yukiko, Agura Kazushi, Fujii Yuka, Yoshiyama Asako, Mashima Kazushi: Sodium methoxide: a simple but highly efficient catalyst for the direct amidation of esters. Chem Commn 2012, 48, 5434. <http://dx.doi.org/10.1039/c2cc32153j>
• Li Wanfang, Fan Weizheng, Ma Xin, Tao Xiaoming, Li Xiaoming, Xie Xiaomin, Zhang Zhaoguo: Ru-catalyzed hydrogenation of 3,5-diketo amides: simultaneous control of chemo- and enantioselectivity. Chem. Commun. 2012, 48, 8976. <http://dx.doi.org/10.1039/c2cc33695b>
• Marrodan Carmen Moreno, Berti Debora, Liguori Francesca, Barbaro Pierluigi: In situ generation of resin-supported Pd nanoparticles under mild catalytic conditions: a green route to highly efficient, reusable hydrogenation catalysts. Catal. Sci. Technol. 2012, 2, 2279. <http://dx.doi.org/10.1039/c2cy20205k>
• Piscopo Calogero G., Bühler Sofie, Sartori Giovanni, Maggi Raimondo: Supported sulfonic acids: reusable catalysts for more sustainable oxidative coupling of xanthene-like compounds with nucleophiles. Catal. Sci. Technol. 2012, 2, 2449. <http://dx.doi.org/10.1039/c2cy20428b>
• Philippe Michel, Didillon Blaise, Gilbert Laurent: Industrial commitment to green and sustainable chemistry: using renewable materials & developing eco-friendly processes and ingredients in cosmetics. Green Chem 2012, 14, 952. <http://dx.doi.org/10.1039/c2gc16341a>
• García-Álvarez Joaquín, Díez Josefina, Vidal Cristian: Pd(ii)-catalyzed cycloisomerisation of γ-alkynoic acids and one-pot tandem cycloisomerisation/CuAAC reactions in water. Green Chem. 2012, 14, 3190. <http://dx.doi.org/10.1039/c2gc36176k>
• Viózquez Santiago F., Bañón-Caballero Abraham, Guillena Gabriela, Nájera Carmen, Gómez-Bengoa Enrique: Enantioselective direct aldol reaction of α-keto esters catalyzed by (Sa)-binam-d-prolinamide under quasi solvent-free conditions. Org. Biomol. Chem. 2012, 10, 4029. <http://dx.doi.org/10.1039/c2ob25224d>
• Singh Maya Shankar, Chowdhury Sushobhan: Recent developments in solvent-free multicomponent reactions: a perfect synergy for eco-compatible organic synthesis. RSC Adv 2012, 2, 4547. <http://dx.doi.org/10.1039/c2ra01056a>
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