Preparation of α-Bromoketones and Thiazoles from Ketones with NBS and Thioamides in Ionic Liquids

Journals Menu

Follow SCIRP

	+1 323-425-8868
	customer@scirp.org
	+86 18163351462(WhatsApp)
	1655362766

	Paper Publishing WeChat

Green and Sustainable Chemistry

ISSN Print: 2160-6951
ISSN Online: 2160-696X
www.scirp.org/journal/gsc
E-mail: gsc@scirp.org

Google-based Impact Factor: 0.71
Citations h5-index & Ranking*

Journals Menu

"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):

Google Scholar
CrossRef

[1]	Synthetic Access to Aromatic α-Haloketones
	Molecules, 2022

[2]	Применение N-галогенсукцинимидов для циклизации с образованием пятичленных гетероциклических соединений
	2020

[3]	Synthesis of Functionalized 1‐Aryl‐3‐phenylthiazolylpropanoids and Their Potential as Anticancer Agents
	2020

[4]	The use of N-halosuccinimides for cyclization with the formation of five-membered heterocyclic compounds
	2020

[5]	Highly efficient and green synthesis of 2, 4-diphenyl substituted thiazoles
	2020

[6]	Ionic liquid assisted synthesis of S-heterocycles
	2019

[7]	Characterization and Computational Studies of 2-(Benzamido) Thiazol-5-yl Benzoate
	2019

[8]	Selective α-bromination of aryl carbonyl compounds: prospects and challenges
	2019

[9]	Characterization and Computational Studies of 2-(Benzamido) Thiazol-5-yl Benzoate.
	2019

[10]	Metal-mediated reactions towards the synthesis of a novel deaminolysed bisurea, dicarbamolyamine
	Open Chemistry, 2018

[11]	Diaryl ethers with carboxymethoxyphenacyl motif as potent HIV-1 reverse transcriptase inhibitors with improved solubility
	Archives of Physiology and Biochemistry, 2018

[12]	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
	SynOpen, 2017

[13]	Analyse par diffraction X et calcul théorique des propriétés structurales des composés organiques à transfert de charges
	2017

[14]	Ball-Milling Promoted Monobromination Reactions: One-pot Regioselective Synthesis of Aryl Bromides and α-Bromoketones by NBS and Recyclable MCM-41 …
	2017

[15]	Sodium bromide-catalyzed oxidation of secondary benzylic alcohols using aqueous hydrogen peroxide as terminal oxidant
	2016

[16]	In (OTf) 3/acid co-catalyzed hydration of 1-haloalkynes to α-halomethyl ketones
	Tetrahedron, 2016

[17]	Au (III)‐Catalyzed Formation of α‐Halomethyl Ketones from Terminal Alkynes
	European journal of organic chemistry, 2016

[18]	ELECTROCATALYTIC OXIDATIVE SIDE CHAIN BROMINATION OF ALKYL ARYL KETONES
	2016

[19]	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

[20]	Solvent and Catalyst Free, Regioselective-Bromination of Aralkyl Ketones Using N-Bromosuccinimide (NBS) Under Microwave Irradiation: An Efficient Protocol
	2015

[21]	SYNTHESIS OF α-HALOBUTENOLIDES USING THE NUCLEOPHILICITY OF MAGNESIUM ALKYLIDENE CARBENOIDS
	HETEROCYCLES, 2015

[22]	Hossein Eshghi, Mehdi Bakavoli, Marjan Ghasemzadeh & Seyed Mohammad Seyedi
	Res Chem Intermed, 2015

[23]	Solvent and catalyst free, regioselective α-bromination of aralkyl ketones using N-bromosuccinimide (NBS) under microwave irradiation: An efficient protocol
	Current Microwave Chemistry, 2015

[24]	Preparation and applications of room temperature ionic liquids in organic synthesis: a review on recent efforts
	Current Green Chemistry, 2015

[25]	Chlorination of aromatic compounds in aqueous media using N-chlorosuccinimide
	2015

[26]	NH4Br–Br2 Catalysed Oxidative Bromination of Aromatic Compounds
	Journal of Agriculture and Life Sciences , 2014

[27]	Oxidative Chlorination of Aromatic Compounds in Aqueous Media
	Journal of Agriculture and Life Sciences, 2014

[28]	Synthesis of α-bromocarbonyl compounds: recent advances
	Tetrahedron, 2014

[29]	Bromination of Enamines from Tertiary Amides Using the Petasis Reagent: A Convenient One-Pot Regioselective Route to Bromomethyl
	Synthetic Communications, 2013

[30]	Биологически активные протонные (2-гидроксиэтил) аммониевые ионные жидкости. Жидкий аспирин
	2012

[31]	Biologically active protic (2-hydroxyethyl) ammonium ionic liquids. Liquid aspirin
	Russian Chemical Bulletin, 2012

[32]	Synthesis, antioxidant and carbonic anhydrase inhibitory potential of Schiff bases of thiazoles
	?Journal of Pharmacy Research?, 2012

[1]	Ionic Liquids as a Non-conventional Catalyst for the Synthesis of N-heterocycles Mini-Reviews in Organic Chemistry, 2024 DOI:10.2174/1570193X20666230507183754

[2]	Synthetic Access to Aromatic α-Haloketones Molecules, 2022 DOI:10.3390/molecules27113583

[3]	Lawesson's reagent promoted deoxygenation of azlactones for the syntheses of 2,4-disubstituted thiazoles Organic & Biomolecular Chemistry, 2022 DOI:10.1039/D2OB01939F

[4]	Lawesson's reagent promoted deoxygenation of azlactones for the syntheses of 2,4-disubstituted thiazoles Organic & Biomolecular Chemistry, 2022 DOI:10.1039/D2OB01939F

[5]	Synthesis of Functionalized 1‐Aryl‐3‐phenylthiazolylpropanoids and Their Potential as Anticancer Agents ChemistrySelect, 2020 DOI:10.1002/slct.202002060

[6]	Highly efficient and green synthesis of 2,4-diphenyl substituted thiazoles Synthetic Communications, 2020 DOI:10.1080/00397911.2020.1718711

[7]	The use of N-halosuccinimides for cyclization with the formation of five-membered heterocyclic compounds Chemistry of Heterocyclic Compounds, 2020 DOI:10.1007/s10593-020-02616-5

[8]	Synthesis of Functionalized 1‐Aryl‐3‐phenylthiazolylpropanoids and Their Potential as Anticancer Agents ChemistrySelect, 2020 DOI:10.1002/slct.202002060

[9]	Ionic liquid assisted synthesis of S-heterocycles Phosphorus, Sulfur, and Silicon and the Related Elements, 2019 DOI:10.1080/10426507.2018.1539492

[10]	Characterization and Computational Studies of 2-(Benzamido)Thiazol-5-yl Benzoate Journal of Structural Chemistry, 2019 DOI:10.1134/S0022476619010190

[11]	Selective α-bromination of aryl carbonyl compounds: prospects and challenges Synthetic Communications, 2019 DOI:10.1080/00397911.2019.1668415

[12]	Diaryl ethers with carboxymethoxyphenacyl motif as potent HIV-1 reverse transcriptase inhibitors with improved solubility Journal of Enzyme Inhibition and Medicinal Chemistry, 2018 DOI:10.1080/14756366.2017.1387542

[13]	Metal-mediated reactions towards the synthesis of a novel deaminolysed bisurea, dicarbamolyamine Open Chemistry, 2018 DOI:10.1515/chem-2018-0058

[14]	AuIII-Catalyzed Formation of α-Halomethyl Ketones from Terminal Alkynes European Journal of Organic Chemistry, 2017 DOI:10.1002/ejoc.201601416

[15]	AuIII‐Catalyzed Formation of α‐Halomethyl Ketones from Terminal Alkynes European Journal of Organic Chemistry, 2017 DOI:10.1002/ejoc.201601416

[16]	In(OTf) 3 /acid co-catalyzed hydration of 1-haloalkynes to α-halomethyl ketones Tetrahedron, 2016 DOI:10.1016/j.tet.2016.04.049

[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 DOI:10.1007/s11164-013-1302-1

[18]	Synthesis of α-bromocarbonyl compounds: recent advances Tetrahedron, 2014 DOI:10.1016/j.tet.2014.04.027

[19]	Bromination of Enamines from Tertiary Amides Using the Petasis Reagent: A Convenient One-Pot Regioselective Route to Bromomethyl Ketones Synthetic Communications, 2013 DOI:10.1080/00397911.2013.765484

[20]	Biologically active protic (2-hydroxyethyl)ammonium ionic liquids. Liquid aspirin Russian Chemical Bulletin, 2012 DOI:10.1007/s11172-012-0172-9

Follow SCIRP

	+1 323-425-8868
	customer@scirp.org
	+86 18163351462(WhatsApp)
	1655362766

	Paper Publishing WeChat

Green and Sustainable Chemistry

Green and Sustainable Chemistry

Journals Menu

Home

About SCIRP

Service

Policies