Fundamentals of green chemistry: efficiency in reaction design.
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[1] R. Sheldon. Chemicals from Synthesis Gas , 2020, Synthesis Gas.
[2] E. García-Junceda. Multi-Step Enzyme Catalysis: Biotransformations and Chemoenzymatic Synthesis , 2008 .
[3] Alle Bruggink,et al. Concepts of Nature in Organic Synthesis: Cascade Catalysis and Multistep Conversions in Concert , 2003 .
[4] R. Sheldon,et al. Pd nanoparticles as catalysts for green and sustainable oxidation of functionalized alcohols in aqueous media , 2010 .
[5] R. Sheldon,et al. Cross-linked enzyme aggregates: a simple and effective method for the immobilization of penicillin acylase. , 2000, Organic letters.
[6] Yong Qin,et al. Palladium nanoparticles confined in the nanocages of SBA-16: Enhanced recyclability for the aerobic oxidation of alcohols in water , 2010 .
[7] Mark J Muldoon,et al. Modern multiphase catalysis: new developments in the separation of homogeneous catalysts. , 2010, Dalton transactions.
[8] R. Sheldon,et al. Catalytic conversions in water. Part 4: Carbonylation of 5-hydroxymethylfurfural (HMF) and benzyl alcohol catalysed by palladium trisulfonated triphenylphosphine complexes , 1997 .
[9] R. Sheldon,et al. Comparison of TEMPO and its derivatives as mediators in laccase catalysed oxidation of alcohols , 2006 .
[10] James G. Stevens,et al. Maximising opportunities in supercritical chemistry: the continuous conversion of levulinic acid to gamma-valerolactone in CO(2). , 2007, Chemical communications.
[11] R. Sheldon,et al. Stabilities and rates in the laccase/TEMPO-catalyzed oxidation of alcohols , 2006 .
[12] Manfred T Reetz,et al. Directed evolution of enantioselective enzymes: an unconventional approach to asymmetric catalysis in organic chemistry. , 2009, The Journal of organic chemistry.
[13] John Andraos,et al. Unification of Reaction Metrics for Green Chemistry: Applications to Reaction Analysis , 2005 .
[14] W. Stemmer. Rapid evolution of a protein in vitro by DNA shuffling , 1994, Nature.
[15] D. Enders,et al. Organocatalysis by N-heterocyclic carbenes. , 2007, Chemical reviews.
[16] Ferdi Schüth,et al. Design of solid catalysts for the conversion of biomass , 2009 .
[17] B. Trost,et al. The atom economy--a search for synthetic efficiency. , 1991, Science.
[18] R. Sheldon,et al. Cu(II)-nitroxyl radicals as catalytic galactose oxidase mimics. , 2003, Organic & biomolecular chemistry.
[19] P. Anastas,et al. Green Chemistry , 2018, Environmental Science.
[20] R. Sheldon. Catalytic reactions in ionic liquids. , 2001, Chemical communications.
[21] James H. Clark,et al. Green chemistry for the second generation biorefinery—sustainable chemical manufacturing based on biomass , 2007 .
[22] R. Rogers,et al. Production of bioactive cellulose films reconstituted from ionic liquids. , 2004, Biomacromolecules.
[23] H. V. Bekkum,et al. The Use of Stable Organic Nitroxyl Radicals for the Oxidation of Primary and Secondary Alcohols , 1997 .
[24] P. Anelli,et al. Fast and selective oxidation of primary alcohols to aldehydes or to carboxylic acids and of secondary alcohols to ketones mediated by oxoammonium salts under two-phase conditions , 1987 .
[25] Michiel Janssen,et al. Room-temperature ionic liquids that dissolve carbohydrates in high concentrations , 2005 .
[26] Peter Licence,et al. Chemical reactions in supercritical carbon dioxide: from laboratory to commercial plantThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13–16th October 2002. , 2003 .
[27] Betina Jørgensen,et al. Formation of acetic acid by aqueous-phase oxidation of ethanol with air in the presence of a heterogeneous gold catalyst. , 2006, Angewandte Chemie.
[28] L. Prati,et al. Gold on Carbon as a New Catalyst for Selective Liquid Phase Oxidation of Diols , 1998 .
[29] Shannon S Stahl,et al. Palladium oxidase catalysis: selective oxidation of organic chemicals by direct dioxygen-coupled turnover. , 2004, Angewandte Chemie.
[30] D. Dess,et al. Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones , 1983 .
[31] Roger A. Sheldon,et al. Synthesis of Aliphatic (S)-α-Hydroxycarboxylic Amides using a One-Pot Bienzymatic Cascade of Immobilised Oxynitrilase and Nitrile Hydratase , 2009 .
[32] M. Fabbrini,et al. An oxidation of alcohols by oxygen with the enzyme laccase and mediation by TEMPO , 2001 .
[33] R. Sheldon,et al. Room Temperature Aerobic Copper–Catalysed Selective Oxidation of Primary Alcohols to Aldehydes , 2004 .
[34] R. Sheldon. Green solvents for sustainable organic synthesis: state of the art , 2005 .
[35] Martyn Poliakoff,et al. Principles of green chemistry: PRODUCTIVELY , 2005 .
[36] David J. C. Constable,et al. Cradle-to-gate life cycle inventory and assessment of pharmaceutical compounds , 2004 .
[37] Geraldine Patricia Taber,et al. A New and Simplified Process for Preparing N-[4-(3,4-Dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine and a Telescoped Process for the Synthesis of (1S-cis)-4-(3,4-Dichlorophenol)-1,2,3,4-tetrahydro-N-methyl-1-naphthalenamine Mandelate: Key Intermediates in the Synthesis of Sertraline , 2004 .
[38] Nicholas J Turner,et al. Directed evolution drives the next generation of biocatalysts. , 2009, Nature chemical biology.
[39] B. Notari. Synthesis and Catalytic Properties of Titanium Containing Zeolites , 1988 .
[40] R. Sheldon,et al. Polymer immobilised TEMPO (PIPO): an efficient catalyst for the chlorinated hydrocarbon solvent-free and bromide-free oxidation of alcohols with hypochlorite , 2000 .
[41] R. Sheldon,et al. Catalytic Conversions in Water. Part 21: Mechanistic Investigations on the Palladium‐Catalysed Aerobic Oxidation of Alcohols in Water† , 2002 .
[42] P. V. Leeuwen. Decomposition pathways of homogeneous catalysts , 2001 .
[43] K. Ebitani,et al. Hydroxyapatite-supported palladium nanoclusters: a highly active heterogeneous catalyst for selective oxidation of alcohols by use of molecular oxygen. , 2004, Journal of the American Chemical Society.
[44] Alan D. Curzons,et al. So you think your process is green, how do you know?—Using principles of sustainability to determine what is green–a corporate perspective , 2001 .
[45] Roger A. Sheldon,et al. Enzyme Immobilization: The Quest for Optimum Performance , 2007 .
[46] David J. C. Constable,et al. Metrics to ‘green’ chemistry—which are the best? , 2002 .
[47] P. Wender,et al. New reactions and step economy: the total synthesis of (±)-salsolene oxide based on the type II transition metal-catalyzed intramolecular [4 + 4] cycloaddition , 2006 .
[48] R. Sheldon,et al. Cross-linked enzyme aggregates (CLEAs): stable and recyclable biocatalysts. , 2007, Biochemical Society transactions.
[49] Roger A. Sheldon,et al. Utilisation of biomass for sustainable fuels and chemicals: Molecules, methods and metrics , 2011 .
[50] F. G. Calvo-Flores. Sustainable chemistry metrics. , 2009, ChemSusChem.
[51] Brian P. Buffin,et al. Electronic, steric, and temperature effects in the Pd(II)-biquinoline catalyzed aerobic oxidation of benzylic alcohols in water , 2008 .
[52] U. Lindstrm,et al. Organic Reactions in Water , 2007 .
[53] K. Nagayama,et al. Size-selective olefin hydrogenation by a Pd nanocluster provided in an apo-ferritin cage. , 2004, Angewandte Chemie.
[54] J. Lange. Lignocellulose conversion: an introduction to chemistry, process and economics , 2007 .
[55] Michele Rossi,et al. The catalytic activity of "naked" gold particles. , 2004, Angewandte Chemie.
[56] Christopher Hardacre,et al. Catalysis in ionic liquids. , 2007, Chemical reviews.
[57] James A. Dumesic,et al. Production of 5-hydroxymethylfurfural and furfural by dehydration of biomass-derived mono- and poly-saccharides , 2007 .
[58] I. Horváth. Solvents from nature , 2008 .
[59] R. Sheldon,et al. Towards greener solvents for the bleach oxidation of alcohols catalysed by stable N-oxy radicals , 2011 .
[60] Jacques Augé,et al. A new rationale of reaction metrics for green chemistry. Mathematical expression of the environmental impact factor of chemical processes , 2008 .
[61] Chao-Jun Li,et al. Green chemistry for chemical synthesis , 2008, Proceedings of the National Academy of Sciences.
[62] Peter J. Dunn,et al. Green chemistry tools to influence a medicinal chemistry and research chemistry based organisation , 2008 .
[63] H. van Bekkum,et al. TEMPO-Mediated Oxidation of Polysaccharides: Survey of Methods and Applications , 2004 .
[64] R. Sheldon,et al. Copper(II)-catalysed aerobic oxidation of primary alcohols to aldehydes. , 2003, Chemical communications.
[65] Juliana Garcia Moretz-Sohn Monteiro,et al. Sustainability metrics for eco-technologies assessment, part I: preliminary screening , 2009 .
[66] Frances H Arnold,et al. Directed enzyme evolution: climbing fitness peaks one amino acid at a time. , 2009, Current opinion in chemical biology.
[67] J. Muzart. Palladium-catalysed oxidation of primary and secondary alcohols , 2003 .
[68] A. Mancuso,et al. Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chloride , 1978 .
[69] S. Stahl,et al. Unexpected roles of molecular sieves in palladium-catalyzed aerobic alcohol oxidation. , 2006, The Journal of organic chemistry.
[70] J. V. van Bokhoven,et al. Deactivation processes of homogeneous Pd catalysts using in situ time resolved spectroscopic techniques. , 2003, Chemical communications.
[71] István T. Horváth,et al. Fluorous Biphase Chemistry , 1998 .
[72] R. Sheldon,et al. Catalytic conversions in water: a novel carbonylation reaction catalysed by palladium trisulfonated triphenylphosphine complexes , 1994 .
[73] Paul T. Anastas,et al. Benign by Design: Alternative Synthetic Design for Pollution Prevention , 1994 .
[74] Marco Eissen,et al. Environmental performance metrics for daily use in synthetic chemistry. , 2002, Chemistry.
[75] Sheldon,et al. Green, catalytic oxidation of alcohols in water , 2000, Science.
[76] John H. Grate,et al. A green-by-design biocatalytic process for atorvastatin intermediate , 2010 .
[77] W. Herrmann,et al. Aqueous-Phase Organometallic Catalysis: Concepts and Applications , 2005 .
[78] Walter Leitner,et al. Supercritical carbon dioxide as a green reaction medium for catalysis. , 2002, Accounts of chemical research.
[79] John C Whitman,et al. Improving catalytic function by ProSAR-driven enzyme evolution , 2007, Nature Biotechnology.
[80] C. Christensen,et al. Chemicals from renewables: aerobic oxidation of furfural and hydroxymethylfurfural over gold catalysts. , 2008, ChemSusChem.
[81] Tomas Hudlicky,et al. Toward a ‘reagent-free’ synthesis , 1999 .
[82] I. Moiseev,et al. Palladium clusters: Stoichiometric and catalytic reactions , 1994 .
[83] M. Muldoon,et al. Anionic N,O-ligated Pd(II) complexes: highly active catalysts for alcohol oxidation. , 2010, Chemical communications.
[84] D. Cole-Hamilton. Asymmetric Catalytic Synthesis of Organic Compounds Using Metal Complexes in Supercritical Fluids , 2006 .
[85] I. Horváth,et al. Facile Catalyst Separation Without Water: Fluorous Biphase Hydroformylation of Olefins , 1994, Science.
[86] Roger A. Sheldon. Atom efficiency and catalysis in organic synthesis , 2000 .
[87] R. Sheldon,et al. Hydrogen Peroxide and Oxygen in Catalytic Oxidation of Carbohydrates and Related Compounds , 1997 .