Online citations, reference lists, and bibliographies.
← Back to Search

Synthesis Of Quinazolinones From Alcohols Via Laccase‐Mediated Tandem Oxidation

M. Heidary, M. Khoobi, S. Ghasemi, Z. Habibi, M. Faramarzi
Published 2014 · Chemistry

Cite This
Download PDF
Analyze on Scholarcy
Share
This paper references
10.1021/CR078380V
Innovations and green chemistry.
I. Horvat́h (2007)
10.1021/cr200185s
Introduction to enzymes in synthesis.
T. Hudlicky (2011)
10.1016/J.MOLCATB.2005.11.001
Preparation and characterization of cross-linked enzyme crystals of laccase
J. J. Roy (2006)
10.1016/J.TET.2003.10.117
Biotransformation of resveratrol: synthesis of trans-dehydrodimers catalyzed by laccases from Myceliophtora thermophyla and from Trametes pubescens
Silvia Nicotra (2004)
10.1039/C3RA46363J
Iron-catalyzed oxidative synthesis of N-heterocycles from primary alcohols
Dan Zhao (2014)
10.1021/JM990131E
New type of febrifugine analogues, bearing a quinolizidine moiety, show potent antimalarial activity against Plasmodium malaria parasite.
Y. Takaya (1999)
10.1081/SCC-120038496
One Pot Synthesis of 4(3H)‐Quinazolinones
B. A. Bhat (2004)
10.1042/BST20060304
Green oxidations with laccase-mediator systems.
A. Wells (2006)
10.1002/EJOC.200390167
Recent Developments in the Isonitrile‐Based Multicomponent Synthesis of Heterocycles
J. Zhu (2003)
10.1016/J.COPBIO.2004.06.011
Trends and innovations in industrial biocatalysis for the production of fine chemicals.
S. Panke (2004)
10.2174/138955711796268778
Synthesis of 2, 3-disubstituted-Quinazolin-4-(3H)-ones.
D. Patil (2011)
10.1248/CPB.23.1910
Studies on organosulfur compounds. XII. Syntheses and pharmacological activities of 2-heterocyclic substituted 4(3H)-quinazolinones.
T. Hisano (1975)
10.7164/ANTIBIOTICS.46.141
Enzymatic dimerization of penicillin X.
H. Agematu (1993)
10.1021/CR0505728
Recent developments in isocyanide based multicomponent reactions in applied chemistry.
A. Dömling (2006)
10.1039/c1ob06516e
Ruthenium-catalysed oxidative synthesis of heterocycles from alcohols.
A. A. Watson (2012)
10.1002/cctc.201200330
Synthesis of Aldehydes by Layer‐by‐Layer Immobilized Laccases in the Presence of Redox Mediators
M. Guazzaroni (2012)
10.1016/j.ejmech.2010.07.063
Synthesis, anti-inflammatory evaluation and docking studies of some new fluorinated fused quinazolines.
C. Balakumar (2010)
10.1016/1381-1169(95)00251-0
A novel method for conversion of benzyl alcohols to benzaldehydes by laccase-catalysed oxidation
A. Potthast (1996)
10.1021/JO00119A006
Selective Enzymic Oxidation of Aromatic Methyl Groups to Aldehydes
A. Potthast (1995)
10.1039/C3RA40872H
Iodine-catalyzed oxidative system for cyclization of primary alcohols with o-aminobenzamides to quinazolinones using DMSO as the oxidant in dimethyl carbonate
Wenlei Ge (2013)
10.1634/THEONCOLOGIST.9-SUPPL_3-10
Dual kinase inhibition in the treatment of breast cancer: initial experience with the EGFR/ErbB-2 inhibitor lapatinib.
H. Burris (2004)
10.1002/ADSC.201300960
Laccase and Laccase‐Mediated Systems in the Synthesis of Organic Compounds
M. Mogharabi (2014)
10.1016/j.jhazmat.2012.01.012
Removal of chlorophenolic derivatives by soil isolated ascomycete of Paraconiothyrium variabile and studying the role of its extracellular laccase.
H. Forootanfar (2012)
10.1002/9783527618262
Enzyme Catalysis in Organic Synthesis
K. Drauz (1995)
10.1016/J.TET.2005.07.010
Synthesis of quinazolinones and quinazolines
David J. Connolly (2005)
10.1016/J.BMCL.2005.01.083
Synthesis and in vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains.
Sheng-li Cao (2005)
10.1039/B507657A
New mediators for the enzyme laccase: mechanistic features and selectivity in the oxidation of non-phenolic substrates
P. Astolfi (2005)
10.1016/S0040-4039(98)01215-5
SYNTHESIS OF AROMATIC ALDEHYDES BY LACCASE-MEDIATOR ASSISTED OXIDATION
E. Fritz-Langhals (1998)
10.1021/jo201054k
One-pot synthesis of quinazolinones via iridium-catalyzed hydrogen transfers.
Jianguang Zhou (2011)
10.1021/CR020033S
The combinatorial synthesis of bicyclic privileged structures or privileged substructures.
D. A. Horton (2003)
10.3998/ARK.5550190.0009.E04
A facile one-pot MW approach for N3-(heteroaryl-2’-yl)- 2-thioxo-2,3-dihydro-1H-quinazolin-4-one
V. K. Tiwari (2008)
10.1016/S1381-1177(00)00184-3
Oxidation of isoeugenol and coniferyl alcohol catalyzed by laccases isolated from Rhus vernicifera Stokes and Pycnoporus coccineus
T. Shiba (2000)
10.1016/j.biortech.2010.09.043
Purification and biochemical characterization of extracellular laccase from the ascomycete Paraconiothyrium variabile.
H. Forootanfar (2011)
10.1021/JM00163A027
Synthesis and anticonvulsant activity of some new 2-substituted 3-aryl-4(3H)-quinazolinones.
J. Wolfe (1990)
10.1021/ol300084v
Synthesis of 3-substituted and 2,3-disubstituted quinazolinones via Cu-catalyzed aryl amidation.
Lanting Xu (2012)
10.1039/C2GC35950B
Laccase-catalyzed oxidation of Hantzsch 1,4-dihydropyridines to pyridines and a new one pot synthesis of pyridines
H. T. Abdel-Mohsen (2012)
10.1002/ANGE.200904622
Ein enantiokomplementäres dirigierendes Protein für die enantioselektive Laccase‐katalysierte oxidative Phenolkupplung
Benjamin Pickel (2010)
10.1002/JPS.3080220804
The constituents of Wu Chü Yü (Evodia rutæcarpa)
A. Chen (1933)
10.1021/JA00449A047
イミノケテンの環状付加反応 II イミノケテンとアミドの縮合反応によるアルボリン,グリコスミニン,およびルテカルピンの全合成
T. Kametani (1977)
10.1021/JM00108A038
Quinazolineacetic acids and related analogues as aldose reductase inhibitors.
M. Malamas (1991)
10.1016/j.bmcl.2009.06.025
Development of a selective and potent radioactive ligand for histamine H(3) receptors: A compound potentially useful for receptor occupancy studies.
Yuko Mitobe (2009)
10.2174/1385272033486477
Laccases and Phenol Oxidases in Organic Synthesis - a Review
S. Burton (2003)
10.1021/JM950692F
Tyrosine kinase inhibitors. 9. Synthesis and evaluation of fused tricyclic quinazoline analogues as ATP site inhibitors of the tyrosine kinase activity of the epidermal growth factor receptor.
G. Rewcastle (1996)
10.1039/B210978F
A study of the oxidation of ethers with the enzyme laccase under mediation by two N–OH–type compounds
Francesca D'Acunzo (2003)
10.1016/J.MOLCATB.2007.09.022
Oxidation of amides by laccase-generated aminoxyl radicals
A. Coniglio (2008)
10.12988/PACS.2013.31018
Laccase-catalyzed synthesis of 4–hydroxycoumarin derivatives
Ghodsieh Bagherzade (2013)
10.1016/J.TET.2005.12.076
Comparison of TEMPO and its derivatives as mediators in laccase catalysed oxidation of alcohols
I. Arends (2006)
10.1016/S0040-4039(01)01463-0
An oxidation of alcohols by oxygen with the enzyme laccase and mediation by TEMPO
M. Fabbrini (2001)
10.2174/1385272033486738
Recent Developments in the Field of Quinazoline Chemistry
Fabiana Witt (2003)
10.1021/JM9506938
Synthesis and hypolipidemic activities of novel 2-[4-[diethoxyphosphoryl)methyl]phenyl]quinazolines and 4(3H)-quinazolinones.
Y. Kurogi (1996)
10.1002/ADSC.200800775
Synthetic Applications of Laccase in Green Chemistry
S. Witayakran (2009)
10.1016/J.BEJ.2011.09.002
Decolorization of some synthetic dyes using optimized culture broth of laccase producing ascomycete Paraconiothyrium variabile
M. Aghaie-Khouzani (2012)
10.1039/B707684C
Total synthesis of luotonin A and 14-substituted analogues
J. J. Mason (2007)
10.1002/anie.200904622
An enantiocomplementary dirigent protein for the enantioselective laccase-catalyzed oxidative coupling of phenols.
B. Pickel (2010)
10.3184/030823400103167381
The Synthesis of Substituted 2-Aryl 4(3H)-Quinazolinones using Nahso3/Dma. Steric Effect upon the Cyclisation-Dehydrogenation Step
S. López (2000)
10.2174/1385272033486747
Preface (Hot Topic: Heterocyclic Chemistry Guest Editor: Jan Bergman)
J. Bergman (2003)



This paper is referenced by
10.1039/C8NJ00195B
Base-promoted ring opening of 3-chlorooxindoles for the construction of 2-aminoarylthioates and their transformation to quinazolin-4(3H)-ones
Tej Narayan Poudel (2018)
10.1002/btpr.2173
Insights into laccase producing organisms, fermentation states, purification strategies, and biotechnological applications
H. Forootanfar (2015)
10.1002/CHIN.201445188
Synthesis of Quinazolinones from Alcohols via Laccase-Mediated Tandem Oxidation.
M. Heidary (2014)
10.4018/978-1-5225-5237-6.CH010
Laccase-Mediated Treatment of Pharmaceutical Wastes
H. Forootanfar (2018)
10.1016/J.JTICE.2015.04.008
Efficient decolorization and detoxification of reactive orange 7 using laccase isolated from Paraconiothyrium variabile, kinetics and energetics
S. Rezaei (2015)
10.1039/C5RA10928K
A catalyst-free rapid, practical and general synthesis of 2-substituted quinazolin-4(3H)-ones leading to luotonin B and E, bouchardatine and 8-norrutaecarpine
K. R. Rao (2015)
10.1016/J.CEJ.2015.09.036
Iron-catalyzed domino sequences: One-pot oxidative synthesis of quinazolinones using metal–organic framework Fe3O(BPDC)3 as an efficient heterogeneous catalyst
V. T. Nguyen (2016)
10.1002/aoc.5899
A novel magnetically separable laccase‐mediator catalyst system for the aerobic oxidation of alcohols and 2‐substituted‐2,3‐dihydroquinazolin‐4(1H)‐ones under mild conditions
Zahra Shokri (2020)
10.1016/J.TET.2015.12.059
Copper-catalyzed consecutive reaction to construct quinazolin-4(3H)-ones and pyrido[2,3-d]pyrimidin-4(3H)-ones
Ting Li (2016)
10.1016/J.TET.2016.01.027
Mechanistic insights into a catalyst-free method to construct quinazolinones through multiple oxidative cyclization
Z. Wang (2016)
10.1039/C4CY01618A
Iron-catalyzed aerobic oxidative functionalization of sp3 C–H bonds: a versatile strategy for the construction of N-heterocycles
X. Chen (2015)
10.1016/J.CATCOM.2015.09.006
Urease: A highly biocompatible catalyst for switchable Biginelli reaction and synthesis of 1,4-dihydropyridines from the in situ formed ammonia
F. Tamaddon (2015)
10.1002/EJOC.201800466
Laccase‐Based Oxidative Catalytic Systems for the Aerobic Aromatization of Tetrahydroquinazolines and Related N‐Heterocyclic Compounds under Mild Conditions
Shaghayegh Saadati (2018)
10.2174/1385272823666190701142930
Isatoic Anhydride: A Fascinating and Basic Molecule for the Synthesis of Substituted Quinazolinones and Benzo di/triazepines
Zahra Tashrifi (2019)
10.1016/J.IBIOD.2015.11.029
Biocatalytic conversion and detoxification of imipramine by the laccase-mediated system
Hamed Tahmasbi (2016)
10.1039/C8RA02827C
2,3-Dihydroquinazolin-4(1H)-one as a privileged scaffold in drug design
M. Badolato (2018)
10.1002/ADSC.201500183
Asymmetric Bio- and Organocatalytic Cascade Reaction – Laccase and Secondary Amine-Catalyzed α-Arylation of Aldehydes
Sanel Suljić (2015)
10.1002/cctc.201701527
Co‐immobilization of Laccase and TEMPO in the Compartments of Mesoporous Silica for a Green and One‐Pot Cascade Synthesis of Coumarins by Knoevenagel Condensation
Mehdi Mogharabi-Manzari (2018)
10.1007/s13738-017-1109-x
Sulfated polyborate: mild, efficient and eco-friendly catalyst for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones
C. K. Khatri (2017)
10.1016/J.IBIOD.2014.10.018
Elimination and detoxification of sulfathiazole and sulfamethoxazole assisted by laccase immobilized on porous silica beads
K. Rahmani (2015)
10.1039/c9ra10303a
Aerobic oxidative synthesis of quinazolinones and benzothiazoles in the presence of laccase/DDQ as a bioinspired cooperative catalytic system under mild conditions
Nadia Ghorashi (2020)
10.1002/slct.201902622
One‐Pot Copper(I)‐Catalyzed Synthesis of 2‐Aryl‐quinazolin‐4(3H)‐ones via N‐ benzylation / Csp3– H Oxidation/ CN Hydrolysis/Cyclization
A. Dandia (2019)
10.1002/cctc.201500142
Enhanced Biocatalytic Performance of Bacterial Laccase from Streptomyces sviceus: Application in the Michael Addition Sequence Towards 3‐Arylated 4‐Oxochromanes
Sanel Suljić (2015)
10.3390/molecules22040673
Production of Laccase by a New Myrothecium verrucaria MD-R-16 Isolated from Pigeon Pea [Cajanus cajan (L.) Millsp.] and its Application on Dye Decolorization
Jiao Sun (2017)
10.1002/SLCT.201700780
Iridium‐Catalyzed Cyclization of o‐Aminobenzamides with Unsaturated Aldehydes to Give 2‐Alkylquinazolinones through a Hydrogen Autotransfer Process
Wei Zhao (2017)
10.1016/J.MOLCATB.2016.02.015
Urease-catalyzed synthesis of aminocyanopyridines from urea under fully green conditions
F. Tamaddon (2016)
Semantic Scholar Logo Some data provided by SemanticScholar