Green and Sustainable Chemistry

Green and Sustainable Chemistry

ISSN Print: 2160-6951
ISSN Online: 2160-696X
www.scirp.org/journal/gsc
E-mail: gsc@scirp.org
"Preparation of α-Bromoketones and Thiazoles from Ketones with NBS and Thioamides in Ionic Liquids"
written by Yuhta Izumisawa, Hideo Togo,
published by Green and Sustainable Chemistry, Vol.1 No.3, 2011
has been cited by the following article(s):
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[3] Highly efficient and green synthesis of 2, 4-diphenyl substituted thiazoles
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[4] Применение N-галогенсукцинимидов для циклизации с образованием пятичленных гетероциклических соединений
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[5] Ionic liquid assisted synthesis of S-heterocycles
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[6] Characterization and Computational Studies of 2-(Benzamido) Thiazol-5-yl Benzoate
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[7] Selective α-bromination of aryl carbonyl compounds: prospects and challenges
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[8] Metal-mediated reactions towards the synthesis of a novel deaminolysed bisurea, dicarbamolyamine
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[9] Diaryl ethers with carboxymethoxyphenacyl motif as potent HIV-1 reverse transcriptase inhibitors with improved solubility
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[10] Ball-Milling Promoted Monobromination Reactions: One-pot Regioselective Synthesis of Aryl Bromides and α-Bromoketones by NBS and Recyclable MCM-41-SO3H at Room Temperature
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[11] Analyse par diffraction X et calcul théorique des propriétés structurales des composés organiques à transfert de charges
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[12] Ball-Milling Promoted Monobromination Reactions: One-pot Regioselective Synthesis of Aryl Bromides and α-Bromoketones by NBS and Recyclable MCM-41 …
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[13] Sodium bromide-catalyzed oxidation of secondary benzylic alcohols using aqueous hydrogen peroxide as terminal oxidant
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[14] In (OTf) 3/acid co-catalyzed hydration of 1-haloalkynes to α-halomethyl ketones
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[15] Au (III)‐Catalyzed Formation of α‐Halomethyl Ketones from Terminal Alkynes
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[16] ELECTROCATALYTIC OXIDATIVE SIDE CHAIN BROMINATION OF ALKYL ARYL KETONES
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[17] Ionic liquids bis(2-N-methylimidazoliumethyl)ether dichloroiodate/dibromochlorate as an efficient halogenating reagent for the synthesis of α-haloketones
Research on Chemical Intermediates, 2015
[18] Solvent and Catalyst Free, Regioselective-Bromination of Aralkyl Ketones Using N-Bromosuccinimide (NBS) Under Microwave Irradiation: An Efficient Protocol
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[19] SYNTHESIS OF α-HALOBUTENOLIDES USING THE NUCLEOPHILICITY OF MAGNESIUM ALKYLIDENE CARBENOIDS
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[20] Hossein Eshghi, Mehdi Bakavoli, Marjan Ghasemzadeh & Seyed Mohammad Seyedi
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[21] Solvent and catalyst free, regioselective α-bromination of aralkyl ketones using N-bromosuccinimide (NBS) under microwave irradiation: An efficient protocol
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[22] Preparation and applications of room temperature ionic liquids in organic synthesis: a review on recent efforts
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[23] Chlorination of aromatic compounds in aqueous media using N-chlorosuccinimide
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[24] NH4Br–Br2 Catalysed Oxidative Bromination of Aromatic Compounds
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[25] Oxidative Chlorination of Aromatic Compounds in Aqueous Media
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[26] Synthesis of α-bromocarbonyl compounds: recent advances
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[27] Bromination of Enamines from Tertiary Amides Using the Petasis Reagent: A Convenient One-Pot Regioselective Route to Bromomethyl
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[28] Биологически активные протонные (2-гидроксиэтил) аммониевые ионные жидкости. Жидкий аспирин
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[29] Biologically active protic (2-hydroxyethyl) ammonium ionic liquids. Liquid aspirin
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[30] Synthesis, antioxidant and carbonic anhydrase inhibitory potential of Schiff bases of thiazoles
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