Optimization of Catalytic Bromination of Acetophenones Using Taguchi's Method
暂无分享,去创建一个
[1] S. Agarwal,et al. The Role of (BDMS) Bromodimethylsulfonium bromide as a Catalyst and Brominating Reagent: A Concise Overview , 2022, ChemistrySelect.
[2] J. Cámpora,et al. NHC-CDI Betaine Adducts and Their Cationic Derivatives as Catalyst Precursors for Dichloromethane Valorization , 2021, The Journal of organic chemistry.
[3] O. R. Shangpliang,et al. Selenium Dioxide-Mediated Bromination of α,β-Unsaturated Ketones Using N-Bromosuccinimide in the Presence of p-Toluenesulfonic Acid: A Versatile Route for the Synthesis of α′-Bromo-4-arylbut-3-en-2-one and α′,α′-Dibromo-4-arylbut-3-en-2-one , 2021, ACS omega.
[4] D. Maiti,et al. Metal-Free Indole-Phenacyl Bromide Cyclization: A Regioselective Synthesis of 3,5-Diarylcarbazoles. , 2020, The Journal of organic chemistry.
[5] S. Karthik,et al. Multi-objective optimization using Taguchi based grey relational analysis in turning of Rock dust reinforced Aluminum MMC , 2020 .
[6] L. Rossi,et al. Green Analysis of the Bromination Reaction of Propiophenone Derivatives Mediated by Cu 2+ Complexes , 2020 .
[7] Akhil Garg,et al. Multivariate optimization for maximum capacity of lead acid battery through Taguchi method , 2019 .
[8] Poonam,et al. Microwave‐Assisted Nanocatalysed Synthesis of Phenacyl Halides as Future Anti‐Platelet Agents , 2019, ChemistrySelect.
[9] Pawan Kumar,et al. Performance optimization of Co2O3-PVDF-CNT-based supercapacitor electrode through multi-response optimization method , 2019, Ionics.
[10] Rajesh H. Vekariya,et al. Phenacyl bromide: A versatile organic intermediate for the synthesis of heterocyclic compounds , 2018, Synthetic Communications.
[11] Jinhui Li,et al. Recycling Tin from Electronic Waste: A Problem That Needs More Attention , 2017 .
[12] Gordon McKay,et al. Waste Printed Circuit Board (PCB) Recycling Techniques , 2017, Topics in Current Chemistry.
[13] J. Safari,et al. Magnetic carbon nanotube‐supported imidazolium cation‐based ionic liquid as a highly stable nanocatalyst for the synthesis of 2‐aminothiazoles , 2016 .
[14] F. Ghorbani,et al. Expeditious green synthesis of 3,4-disubstituted isoxazole-5(4H)-ones catalyzed by nano-MgO , 2016, Research on Chemical Intermediates.
[15] Zhanhu Guo,et al. Selective Desoldering Separation of Tin–Lead Alloy for Dismantling of Electronic Components from Printed Circuit Boards , 2015 .
[16] K. Krishnamoorthy,et al. Mechanistic investigation on the toxicity of MgO nanoparticles toward cancer cells , 2012 .
[17] R. Ananthakrishnan,et al. Bromodimethylsulfonium bromide as a potential candidate for photocatalytic selective oxidation of benzylic alcohols using oxygen and visible light , 2012 .
[18] H. Meshram,et al. DABCO-Promoted Efficient and Convenient Synthesis of Benzofurans , 2012 .
[19] G. Olah,et al. α-Halogenation of carbonyl compounds: halotrimethylsilane–nitrate salt couple as an efficient halogenating reagent system , 2011 .
[20] L. Yadav,et al. Bromodimethylsulfonium bromide (BDMS)-catalyzed multicomponent synthesis of 3-aminoalkylated indoles , 2010 .
[21] A. T. Khan,et al. Bromodimethylsulfonium bromide (BDMS) mediated dithioacetalization of carbohydrates under solvent-free conditions. , 2010, Carbohydrate research.
[22] J. Brion,et al. MPHT-Promoted Bromocyclization of ortho-Substituted Arylalkynes: Application to the Synthesis of 2-Substituted 3-Bromobenzofurans and -Benzo[b]thiophenes , 2010 .
[23] G. Shankarling,et al. Halogenation reactions in biodegradable solvent: Efficient bromination of substituted 1-aminoanthra-9,10-quinone in deep eutectic solvent (choline chloride : urea) , 2010 .
[24] A. T. Khan,et al. Recent advances in the application of bromodimethylsulfonium bromide (BDMS) in organic synthesis , 2009 .
[25] J. Nath,et al. Boric acid catalyzed bromination of a variety of organic substrates: an eco-friendly and practical protocol , 2008 .
[26] Babulal Das,et al. Metal Free One Pot Approach Towards the Synthesis of Hantzsch Esters and their Application as the Hydrogen Source for the Reduction of Activated Olefins Catalysed by Bromo Dimethyl Sulfonium Bromide (BDMS) , 2008 .
[27] A. T. Khan,et al. A Mild and Regioselective Method for α-Bromination of β-Keto Esters and 1,3-Diketones Using Bromodimethylsulfonium Bromide (BDMS) , 2006 .
[28] M. Krishnaiah,et al. Sulfonic acid functionalized silica : A remarkably efficient heterogeneous reusable catalyst for α-monobromination of carbonyl compounds using N-bromosuccinimide , 2006 .
[29] S. Ghosh,et al. Bromodimethylsulfonium bromide: A useful reagent for acylation of alcohols, phenols, amines, thiols, thiophenols and 1,1-diacylation of aldehydes under solvent free conditions , 2005 .
[30] B. Das,et al. A simple and efficient method for α-bromination of carbonyl compounds using N-bromosuccinimide in the presence of silica-supported sodium hydrogen sulfate as a heterogeneous catalyst , 2005 .
[31] A. T. Khan,et al. A highly efficient and catalytic synthetic protocol for oxathioacetalization of carbonyl compounds , 2005 .
[32] S. Ghosh,et al. A Simple and Practical Synthetic Protocol for Acetalisation, Thioacetalisation and Transthioacetalisation of Carbonyl Compounds under Solvent-Free Conditions , 2004 .
[33] S. Ghosh,et al. A Highly Efficient and Chemoselective Synthetic Protocol for Tetrahydropyranylation/Depyranylation of Alcohols and Phenols , 2003 .
[34] Takayuki Suzuki,et al. Synthesis of optically active alpha-aminoalkyl alpha'-halomethyl ketone: a cross-Claisen condensation approach. , 2002, Organic letters.
[35] R. Hoffman,et al. Highly Stereoselective Synthesis of an ti -N-Protected-a-Amino Epoxides , 2001 .
[36] S. Kajigaeshi,et al. Synthesis of dibromoacetyl derivatives by use of benzyltrimethylammonium tribromide , 1987 .
[37] Y. Chow,et al. The electrophilic addition of dimethylbromosulfonium bromide to conjugated enones: efficient synthesis of α-bromo enones , 1982 .
[38] G. Olah,et al. Synthetic Methods and Reactions; 69 1 . Dethioacetalization with Bromodimethylsulfonium Bromide , 1979 .
[39] Seung Jun Lee,et al. Efficient microwave induced direct α-halogenation of carbonyl compounds , 2004 .