Flash flow pyrolysis: mimicking flash vacuum pyrolysis in a high-temperature/high-pressure liquid-phase microreactor environment.
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Hassan Sheibani | David Cantillo | C. Kappe | C. Kappe | C Oliver Kappe | David Cantillo | H. Sheibani
[1] Jun-ichi Yoshida,et al. Green and sustainable chemical synthesis using flow microreactors. , 2011, ChemSusChem.
[2] A. Gaber,et al. Synthetic Applications of the Pyrolysis of Meldrum’s Acid Derivatives , 2001 .
[3] P. Feldman,et al. Ketenes. 20. Thermal decomposition of 2,2,6-trimethyl-4H-1,3-dioxin-4-one and 1-ethoxybutyn-3-one. Acetylketene , 1984 .
[4] D. Cremer,et al. Vibrational spectrum of m-benzyne: a matrix isolation and computational study. , 2002, Journal of the American Chemical Society.
[5] C. Wentrup,et al. Oxoketene-oxoketene, imidoylketene-imidoylketene and oxoketenimine-imidoylketene rearrangements. 1,3-Shifts of phenyl groups. , 2006, Organic & biomolecular chemistry.
[6] E. Heilbronner,et al. Spektrographische und thermochemische Untersuchungen an dampfförmigem Azulen , 1947 .
[7] L. T. Scott,et al. Thermal rearrangements of aromatic compounds , 1982 .
[8] W. Meutermans,et al. (Cyanovinyl)ketenes from azafulvenones. An apparent retro-Wolff rearrangement , 1996 .
[9] G. Seybold. Flash Thermolysis of Organic Compounds , 1977 .
[10] Yutaka Yamamoto,et al. CONVENIENT PREPARATION OF TRIFLUOROACETYL MELDRUM'S ACID AND ITS USE AS A BUILDING BLOCK FOR TRIFLUOROMETHYL-CONTAINING COMPOUNDS , 1997 .
[11] Ryan L. Hartman,et al. Deciding whether to go with the flow: evaluating the merits of flow reactors for synthesis. , 2011, Angewandte Chemie.
[12] Toma Glasnov,et al. Highlights from the Flow Chemistry Literature 2011 (Part 1) , 2011, Journal of Flow Chemistry.
[13] C. Wiles,et al. Continuous flow reactors: a perspective , 2012 .
[14] K. Merz,et al. Thermal rearrangements of C10H8 species; benzvalene analogues and the automerization of naphthalene , 1986 .
[15] Alajarin,et al. Conversion of N-acyl-4-acyloxy-beta-lactams into 1,3-oxazin-6-ones: two consecutive pseudopericyclic processes , 2000, Organic letters.
[16] M. Karpf. Organic Synthesis at High Temperatures. Gas‐Phase Flow Thermolysis [New Synthetic Methods (57)] , 1986 .
[17] C. Wentrup,et al. Azulene-naphthalene rearrangement. Involvement of 1-phenylbuten-3-ynes and 4-phenyl-1,3-butadienylidene , 1980 .
[18] K. Merz,et al. The C10H8 potential energy surface: the azulene-to-naphthalene rearrangement , 1986 .
[19] C. Cramer,et al. Universal solvation model based on solute electron density and on a continuum model of the solvent defined by the bulk dielectric constant and atomic surface tensions. , 2009, The journal of physical chemistry. B.
[20] G. Burdziński,et al. Ultrafast spectroscopic and matrix isolation studies of p-biphenylyl, o-biphenylyl, and 1-naphthylnitrenium cations. , 2007, Journal of the American Chemical Society.
[21] R. Alder,et al. Thermolysis of 2-methylazulene(1-carbon-13) and mechanism of the azulene to naphthalene rearrangement , 1979 .
[22] S. Bräse,et al. Microwave‐Assisted Stereoselective One‐Pot Synthesis of Symmetrical and Unsymmetrical 2,5‐Diketopiperazines from Unprotected Amino Acids , 2008 .
[23] B. Grenon,et al. The decarbethoxylation of geminal dicarbethoxy compounds. , 1967, Tetrahedron letters.
[24] K. Bidasee,et al. Streptozotocin-Induced Diabetes Increases Disulfide Bond Formation on Cardiac Ryanodine Receptor (RyR2) , 2003, Journal of Pharmacology and Experimental Therapeutics.
[25] Steven V. Ley,et al. The flow synthesis of heterocycles for natural product and medicinal chemistry applications , 2011, Molecular Diversity.
[26] Paul Watts,et al. Recent advances in micro reaction technology. , 2011, Chemical communications.
[27] R. Clemens,et al. Acetoacetylation with 2,2,6-trimethyl-4H-1,3-dioxin-4-one: a convenient alternative to diketene , 1985 .
[28] Toma N. Glasnov,et al. Highlights from the Flow Chemistry Literature 2011 (Part 2) , 2011 .
[29] C. Wentrup,et al. Imidoylketene-oxoketenimine interconversion. Rearrangement of a carbomethoxyketenimine to a methoxyimidoylketene and 2-methoxy-4-quinolone , 1996 .
[30] C. Wentrup,et al. Cumulene Rearrangements: Ketene-Ketene, Isocyanate-Isocyanate, Thioketene-Ketene, Imidoylketene-Ketenimine, and Ketene-Allene Rearrangements , 2010 .
[31] C. Kappe,et al. Heterogeneous versus homogeneous palladium catalysts for ligandless mizoroki-heck reactions: a comparison of batch/microwave and continuous-flow processing. , 2009, Chemistry.
[32] S. Ham,et al. Chemoselectivity in the Reactions of Acetylketene and Acetimidoylketene: Confirmation of Theoretical Predictions. , 1997, The Journal of organic chemistry.
[33] D. Birney,et al. Microwave generation and trapping of acetylketene , 2008 .
[34] B. Freiermuth,et al. Direct observation of α-oxo ketenes formed from 1,3-dioxin-4-ones and the enols of β-keto esters , 1991 .
[35] T. Wirth,et al. Microreactors in organic synthesis and catalysis , 2008 .
[36] Su Jin Kim,et al. Facile synthesis of reduced graphene oxide in supercritical alcohols and its lithium storage capacity , 2011 .
[37] C. Kappe,et al. The microwave-to-flow paradigm: translating high-temperature batch microwave chemistry to scalable continuous-flow processes. , 2011, Chemistry.
[38] M. Stevens,et al. Antitumour polycyclic acridines. Part 1. Synthesis of7H-pyrido- and 8H-quino-[4,3,2-kl]acridinesby Graebe–Ullmann thermolysis of 9-(1,2,3-triazol-1-yl)acridines:application of differential scanning calorimetry to predict optimumcyclisation conditions , 1997 .
[39] Nils Pemberton,et al. Synthesis of multi ring-fused 2-pyridones via an acyl-ketene imine cyclocondensation. , 2006, Organic letters.
[40] H. W. Moore,et al. Conjugated ketenes: new aspects of their synthesis and selected utility for the synthesis of phenols, hydroquinones, and quinones , 1986 .
[41] W. Stadlbauer,et al. DSC — A Valuable Tool in Heterocyclic Synthesis , 1997 .
[42] D. Roberge,et al. Safe Generation and Synthetic Utilization of Hydrazoic Acid in a Continuous Flow Reactor , 2012, Journal of Flow Chemistry.
[43] C. Wentrup,et al. Force field-SCF calculations on cyclopropene intermediates in carbene rearrangements. Comparison with experiment , 1985 .
[44] A. Lovey,et al. Decarbalkoxylations of geminal diesters and β-keto esters in wet dimethyl sulfoxide. Effect of added sodium chloride on the decarbalkoxylation rates of mono- and di-substituted Malonate esters , 1974 .
[45] R. Fausto,et al. The pyrolysis of isoxazole revisited: a new primary product and the pivotal role of the vinylnitrene. A low-temperature matrix isolation and computational study. , 2011, Journal of the American Chemical Society.
[46] Moer,et al. Felkin-Anh stereoselectivity in cycloadditions of acetylketene: evidence for a concerted, pseudopericyclic pathway , 2000, The Journal of organic chemistry.
[47] Ulf Tilstam,et al. The Newman−Kwart Rearrangement Revisited: Continuous Process under Supercritical Conditions† , 2009 .
[48] J. Foot,et al. An empirical study of the effect of the variables in a flash vacuum pyrolysis (FVP) experiment. , 2004, Organic & biomolecular chemistry.
[49] W. Stadlbauer,et al. Heteroelectrocyclic reaction of 4‐azido‐3‐hydrazonoalkyl‐quinolines to 2‐arylaminopyrazolo[4,3‐c]quinolones , 2000 .
[50] Qingwei Zhang,et al. Asymmetric Synthesis of an HIV Protease Inhibitor via a Novel .alpha.-Oxoketene/Ketene [4 + 2] Cycloaddition Reaction , 1994 .
[51] Richard P. Johnson,et al. Microwave flash pyrolysis. , 2009, The Journal of organic chemistry.
[52] Y. Morita,et al. 1,3-Oxazines and related compounds. XII: Facile synthesis of 2,4-disubstituted 6H-1,3-oxazin-6-ones , 1986 .
[53] Klavs F Jensen,et al. Integrated microreactors for reaction automation: new approaches to reaction development. , 2010, Annual review of analytical chemistry.
[54] C. Kappe,et al. Microwave-assisted and continuous flow multistep synthesis of 4-(pyrazol-1-yl)carboxanilides. , 2011, The Journal of organic chemistry.
[55] C. Kappe,et al. ACETYLKETENE : CONFORMATIONAL ISOMERISM AND PHOTOCHEMISTRY MATRIX ISOLATION INFRARED AND AB INITIO STUDIES , 1995 .
[56] Falk Morawitz,et al. Synthesis of Annulated Pyridines by Intramolecular Inverse‐Electron‐Demand Hetero‐Diels–Alder Reaction under Superheated Continuous Flow Conditions , 2012 .
[57] Yutaka Yamamoto,et al. 1,3-Oxazines and related compounds. XIII: Reaction of acyl Meldrum's acids with Schiff bases giving 2,3-disubstituted 5-acyl-3,4,5,6-tetrahydro-2H-1,3-oxazine-4,6-diones and 2,3,6-trisubstituted 2,3-dihydro-1,3-oxazin-4-ones , 1987 .
[58] S. Kim,et al. High Molecular Weight Poly(L-lactide) and its Microsphere Synthesized in the Supercritical Dimethyl Ether , 2007 .
[59] Toma N. Glasnov,et al. Accessing Novel Process Windows in a High-Temperature/Pressure Capillary Flow Reactor , 2009 .
[60] W. Sander,et al. Matrix isolation, spectroscopic characterization, and photoisomerization of m-xylylene. , 2008, Journal of the American Chemical Society.
[61] W. Leitner,et al. Chemical Synthesis Using Supercritical Fluids: Jessop/Chemical , 2007 .
[62] P. Plattner,et al. Umlagerung von Azulen in Naphthalin , 1947, Experientia.
[63] M. Fischer,et al. Thermal cyclization of 4-azido-3-nitropyridines to furoxanes† , 2000 .
[64] Alessandro Laio,et al. Azulene-to-naphthalene rearrangement: the Car-Parrinello metadynamics method explores various reaction mechanisms. , 2004, Chemphyschem : a European journal of chemical physics and physical chemistry.
[65] H. Butenschön. Synthesis of 5-Methoxy- and 5-(Dialkylamino)bicyclo[3.2.0]hept-2-en-6-one Derivatives by cine Substitution with Methoxide Anions and Dialkylamines , 1994 .
[66] C. Wentrup,et al. Imidoylketene - oxoketenimine rearrangement. Facile 1,3-shift of an alkoxy group , 1995 .
[67] O. Yonemitsu,et al. Meldrum's acid in organic synthesis. 2. A general and versatile synthesis of .beta.-keto esters , 1978 .
[68] S. Ley,et al. An efficient and transition metal free protocol for the transfer hydrogenation of ketones as a continuous flow process , 2009 .
[69] Andreas Kirschning,et al. Ten key issues in modern flow chemistry. , 2011, Chemical communications.
[70] Masayuki Sato,et al. Synthesis of β-Ketocarboxamide Derivatives Using 2,2-Dimethyl-2H, 4H-1,3-dioxin-4-ones , 1984 .
[71] S. Parsons,et al. Synthetic routes to pyrrolizine-1,5-dione derivatives by flash vacuum pyrolysis of amidomethylene derivatives of Meldrum's acid. , 2009, Organic & biomolecular chemistry.
[72] L. Castedo,et al. Synthesis of 3-phenylisoquinolones by reaction of simple pyrroline-2,3-diones with benzyne. New mechanistic considerations , 1993 .
[73] C. Oliver Kappe,et al. Translating High-Temperature Microwave Chemistry to Scalable Continuous Flow Processes , 2010 .
[74] Timothy Noël,et al. Cross-coupling in flow. , 2011, Chemical Society reviews.
[75] K. Merz,et al. Mechanism of the azulene to naphthalene rearrangement , 1985 .
[76] C. Oliver Kappe,et al. Continuous‐Flow Microreactor Chemistry under High‐Temperature/Pressure Conditions , 2009 .
[77] E. Kolehmainen,et al. Cyclic dipeptides: catalyst/promoter-free, rapid and environmentally benign cyclization of free amino acids , 2011 .
[78] D. Truhlar,et al. The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionals , 2008 .
[79] F. Diederich,et al. Solution-spray flash vacuum pyrolysis: a new method for the synthesis of linear poliynes with odd numbers of C.tplbond.C bonds from substituted 3,4-dialkynyl-3-cyclobutene-1,2-diones , 1991 .
[80] A. Lovey,et al. Synthetic applications and mechanism studies of the decarbalkoxylations of geminal diesters and related systems effected in dimethyl sulfoxide by water and/or by water with added salts , 1978 .
[81] H. Mcnab,et al. Synthesis of 2-substituted 1,3-oxazin-6-ones by gas-phase pyrolysis , 1996 .
[82] H. Reisenauer,et al. Complex of silylene with nitrogen: a combined matrix-spectroscopic and density functional theory study. , 2006, Chemistry, an Asian journal.
[83] F. Almqvist,et al. An enantioselective ketene-imine cycloaddition method for synthesis of substituted ring-fused 2-pyridinones. , 2001, The Journal of organic chemistry.
[84] V. Hessel,et al. Flow chemistry using milli- and microstructured reactors-from conventional to novel process windows. , 2010, Bioorganic & medicinal chemistry.
[85] C. Oliver Kappe,et al. On the importance of simultaneous infrared/fiber-optic temperature monitoring in the microwave-assisted synthesis of ionic liquids. , 2010, Organic & biomolecular chemistry.
[86] A. Arrieta,et al. On the mechanism of conversion of N-acyl-4-acyloxy-beta-lactams into 2-substituted 1,3-oxazin-6-ones. Can a low-barrier transition state be antiaromatic? , 2001, The Journal of organic chemistry.
[87] Bernhard Gutmann,et al. Microwave chemistry in silicon carbide reaction vials: separating thermal from nonthermal effects. , 2009, Angewandte Chemie.
[88] Masayuki Sato,et al. Synthesis of 1, 3-Dioxin-4-one Derivatives , 1983 .
[89] Toma Glasnov,et al. Highlights from the Flow Chemistry Literature 2011 (Part 3) , 2012, Journal of Flow Chemistry.
[90] E. Akbas,et al. Synthesis and spectral studies of pyranone derivative and its Cu(II), Co(II), Ni(II) and Zn(II) complexes , 2008 .
[91] C. Oliver Kappe,et al. Continuous flow organic synthesis under high-temperature/pressure conditions. , 2010, Chemistry, an Asian journal.
[92] H. Butenschön. Ring Opening of (η5‐Bicyclo[3.2.0]hepta‐1,3‐dienyl)‐(η4‐tetraphenylcyclobutadiene)cobalt(I) Followed by Cycloaddition , 1993 .
[93] Hye-Min Choi,et al. Continuous synthesis of metal nanoparticles in supercritical methanol , 2010 .
[94] G. Marshall,et al. Stereoselective synthesis of optically active beta-lactams, potential inhibitors of pilus assembly in pathogenic bacteria. , 2000, Organic letters.