Zobrazeno 1 - 10 of 76 pro vyhledávání: '"4-HYDROXYACETOPHENONE MONOOXYGENASE"'
1
Polycyclic Ketone Monooxygenase (PockeMO)
Autor: Marco W. Fraaije, Maximilian J. L. J. Fürst, Gonzalo de Gonzalo
Publikováno v: Catalysts
idUS. Depósito de Investigación de la Universidad de Sevilla
instname
Catalysts; Volume 7; Issue 10; Pages: 288
Catalysts, 7(10):288, 1-10. MDPI AG
Catalysts, Vol 7, Iss 10, p 288 (2017)
recently discovered, moderately thermostable Baeyer-Villiger monooxygenase, polycyclic ketone monooxygenase (PockeMO), from Thermothelomyces thermophila has been employed as a biocatalyst in a set of asymmetric sulfoxidations. The enzyme was able to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f1e622f7b825e9607635dc90b90a757
https://hdl.handle.net/11370/a5473fb1-19c8-42bb-88fb-e63105dff755
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2
Discovery of Baeyer-Villiger monooxygenases from photosynthetic eukaryotes
Autor: Mattia Niero, Riccardo Motterle, Elisa Beneventi, Elisabetta Bergantino, Marco W. Fraaije
Publikováno v: Journal of Molecular Catalysis B: Enzymatic, 98, 145-154. ELSEVIER SCIENCE BV
Baeyer-Villiger monooxygenases are attractive "green" catalysts able to produce chiral esters or lactones starting from ketones. They can act as natural equivalents of peroxyacids that are the catalysts classically used in the organic synthesis react
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f81fd8150ff3af4f96e4be9b30f8173a
https://doi.org/10.1016/j.molcatb.2013.10.006
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3
Selective Oxidations of Organoboron Compounds Catalyzed by Baeyer-Villiger Monooxygenases
Autor: Gonzalo de Gonzalo, Leandro H. Andrade, Patrícia B. Brondani, Marco W. Fraaije
Publikováno v: Advanced Synthesis & Catalysis, 353(11-12), 2169-2173. WILEY-V C H VERLAG GMBH
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
The applicability of Baeyer-Villiger monooxygenases (BVMOs) in organoboron chemistry has been explored through testing chemo-and enantioselective oxidations of a variety of boron-containing aromatic and vinylic compounds. Several BVMOs, namely: pheny
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f747212fdf0cd8d4762a9bdb0d8705d
https://hdl.handle.net/11370/94400bfb-d56d-4bc7-98ff-480f035efe94
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4
Enzymatic Synthesis of Novel Chiral Sulfoxides Employing Baeyer-Villiger Monooxygenases
Autor: Gonzalo de Gonzalo, Marco W. Fraaije, Daniel E. Torres Pazmino, Vicente Gotor, Ana Rioz-Martínez
Publikováno v: European Journal of Organic Chemistry, 2010(33), 6409-6416. WILEY-V C H VERLAG GMBH
Optically active sulfoxides are compounds of high interest in organic chemistry. Herein, we report the preparation of a set of chiral heteroaryl alkyl, cyclohexyl alkyl, and alkyl alkyl sulfoxides by using enantioselective sulfoxidation reactions emp
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e53428780c59376e29e09ee30f8f94aa
https://doi.org/10.1002/ejoc.201000890
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5
Synthesis of Chiral 3-Alkyl-3,4-dihydroisocoumarins by Dynamic Kinetic Resolutions Catalyzed by a Baeyer−Villiger Monooxygenase
Autor: Marco W. Fraaije, Gonzalo de Gonzalo, Ana Rioz-Martínez, Daniel E. Torres Pazmino, Vicente Gotor
Publikováno v: Journal of Organic Chemistry, 75(6), 2073-2076. AMER CHEMICAL SOC INC
Baeyer-Villiger monooxygenases have been tested in the oxidation of racemic benzofused ketones. When employing a single Mutant of phenylacetone monooxygenase (M446G PAMO) under the proper reaction conditions, it was possible to achieve 3-substituted
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fefbc56617bfaa3e093c3f8b8cf810b0
https://doi.org/10.1021/jo902519j
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6
Baeyer-Villiger monooxygenase-catalyzed kinetic resolution of racemic alpha-alkyl benzyl ketones
Autor: Daniel E. Torres Pazmino, Gonzalo de Gonzalo, Vicente Gotor, Cristina Rodríguez, Marco W. Fraaije
Publikováno v: Tetrahedron: Asymmetry
Tetrahedron-Asymmetry, 20(10), 1168-1173. PERGAMON-ELSEVIER SCIENCE LTD
The application of three BVMOs for the enantioselective oxidation of 3-phenylbutan-2-ones with different substituents in the aromatic moiety is described. By choosing the appropriate biocatalyst and substrate combination, chiral ketones and esters ca
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3178f2097e76effc43e1168364b103d8
https://research.rug.nl/en/publications/411ac8c1-9e39-421d-9f1d-86ad350b58af
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7
Kinetic mechanism of phenylacetone monooxygenase from Thermobifida fusca
Autor: Torres Pazmiño, Daniel E., Baas, Bert-Jan, Janssen, Dick B., Fraaije, Marco W., Gonzalo, Gonzalo de, Ottolina, Gianluca, Carrea, Giacomo
Publikováno v: Biochemistry, 47(13), 4082-4093. AMER CHEMICAL SOC
Phenylacetone monooxygenase (PAMO) from Thermobifida fusca is a FAD-containing Baeyer-Villiger monooxygenase (BVMO). To elucidate the mechanism of conversion of phenylacetone by PAMO, we have performed a detailed steady-state and pre-steady-state kin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4095d1741870f1901d13f27727b6c39f
https://research.rug.nl/en/publications/41c68e60-1342-4395-90f0-d70195ca9975
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9
Enzymatic kinetic resolution of racemic ketones catalyzed by Baeyer-Villiger monooxygenases
Autor: Gonzalo de Gonzalo, Vicente Gotor, Cristina Rodríguez, Marco W. Fraaije
Publikováno v: Tetrahedron-Asymmetry, 18(11), 1338-1344. PERGAMON-ELSEVIER SCIENCE LTD
A set of racemic cyclic and linear ketones, as well as 2-phenylpropionaldehyde, were tested as substrates in the enzymatic Baeyer-Villiger oxidation catalyzed by two Baeyer-Villiger monooxygenases: phenylacetone monooxygenase (PAMO) and 4-hydroxyacet
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5ba60bfd915bac3fd12991168bf3b3b
https://research.rug.nl/en/publications/c9c94467-9961-4515-851a-5ad10415b792
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10
Oxidations catalyzed by phenylacetone monooxygenase from Thermobifida fusca
Autor: Gonzalo de Gonzalo, Gianluca Ottolina, Marco W. Fraaije, Giacomo Carrea, Daniel E. Torres Pazmino
Publikováno v: Tetrahedron: asymmetry
16 (2005): 3077–3083. doi:10.1016/j.tetasy.2005.08.004
info:cnr-pdr/source/autori:de Gonzalo G., Pazmino D.E.T., Ottolina G., Fraaije M.W., Carrea G./titolo:Oxidations catalyzed by phenylacetone monooxygenase from Thermobifida fusca/doi:10.1016%2Fj.tetasy.2005.08.004/rivista:Tetrahedron: asymmetry (Print)/anno:2005/pagina_da:3077/pagina_a:3083/intervallo_pagine:3077–3083/volume:16
Tetrahedron-Asymmetry, 16(18), 3077-3083. PERGAMON-ELSEVIER SCIENCE LTD
Several organic sulfides, ketones and other organic systems have been tested as substrates in oxidation reactions catalyzed by the recently discovered phenylacetone monooxygenase from Thermobifida fusca. The biocatalytic properties of this Baeyer–V
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c64568dc5490d7e20099ab140d9ea11
https://doi.org/10.1016/j.tetasy.2005.08.004
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