4.6 Article

Chemospecific and ligand free CuI catalysed heterogeneous N-arylation of amines with diheteroaryl halides at room temperature

期刊

ORGANIC & BIOMOLECULAR CHEMISTRY
卷 9, 期 5, 页码 1324-1327

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0ob00859a

关键词

-

向作者/读者索取更多资源

A ligand free, copper-catalyzed N-arylation reaction of amines with diheteroaryl halides in heterogeneous medium at room temperature has been developed. The protocol is very effective for low boiling amines and useful for amines available in aqueous solution. The reaction gives chemospecific arylation of amines with diheteroaryl halides in the mixture monoheteroaryl halides, diheteroaryl halides and carbocyclic aryl halides. The reaction is also chemospecific with respect to arylation of aliphatic amines. Monoarylated piperazines were also synthesized at room temperature following this protocol.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Biochemistry & Molecular Biology

Synthesis and in vitro kinetic evaluation of N-thiazolylacetamido monoquaternary pyridinium oximes as reactivators of sarin, O-ethylsarin and VX inhibited human acetylcholinesterase (hAChE)

Aditya Kapil Valiveti, Uma M. Bhalerao, Jyotiranjan Acharya, Hitendra N. Karade, Badri Narayan Acharya, G. Raviraju, Anand K. Halve, Mahabir Parshad Kaushik

BIOORGANIC & MEDICINAL CHEMISTRY (2015)

Article Chemistry, Multidisciplinary

SNAr reaction in aqueous medium in the presence of mixed organic and inorganic bases

Nilesh B. Shelke, Ramrao Ghorpade, Ajay Pratap, Vijay Tak, B. N. Acharya

RSC ADVANCES (2015)

Article Biochemistry & Molecular Biology

Synthesis and in vitro reactivation study of isonicotinamide derivatives of 2-(hydroxyimino)-N-(pyridin-3-yl)acetamide as reactivators of Sarin and VX inhibited human acetylcholinesterase (hAChE)

Hitendra N. Karade, G. Raviraju, B. N. Acharya, Aditya Kapil Valiveti, Uma Bhalerao, Jyotiranjan Acharya

BIOORGANIC & MEDICINAL CHEMISTRY (2016)

Article Chemistry, Medicinal

Synthesis and antimalarial evaluation of 1, 3, 5-trisubstituted pyrazolines

Badri Narayan Acharya, Deepika Saraswat, Mugdha Tiwari, Asish Kumar Shrivastava, Ramarao Ghorpade, Saroj Bapna, Mahabir Parshad Kaushik

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2010)

Article Chemistry, Medicinal

Design, synthesis, and antimalarial evaluation of thiazole-derived amino acids

Hitendra N. Karade, B. N. Acharya, Manisha Sathe, M. P. Kaushik

MEDICINAL CHEMISTRY RESEARCH (2008)

Article Chemistry, Medicinal

Antimalarial activity of Gomphostemma crinitum leaf extracts

Badri Narayan Acharya, Deepika Saraswat, Mahabir Parshad Kaushik

MEDICINAL CHEMISTRY RESEARCH (2008)

Article Chemistry, Medicinal

Design, synthesis, and evaluation of dihydropyrimidinone (DHPM) based muscarinic receptor antagonist

Badri N. Acharya, G. B. Dharma Rao, Deo Kumar, Pravin Kumar, Mahabir P. Kaushik

MEDICINAL CHEMISTRY RESEARCH (2015)

Article Chemistry, Organic

Imidazole-Catalyzed Monoacylation of Symmetrical Diamines

Sanjeev K. Verma, B. N. Acharya, M. P. Kaushik

ORGANIC LETTERS (2010)

Article Chemistry, Organic

N,N′-Dichlorobis(2,4,6-trichlorophenyl)urea (CC-2) as a new reagent for the synthesis of pyrimidone and pyrimidine derivatives via Biginelli reaction

G. B. Dharma Rao, B. N. Acharya, S. K. Verma, M. P. Kaushik

TETRAHEDRON LETTERS (2011)

Article Chemistry, Multidisciplinary

A DBU-diheteroaryl halide adduct as the fastest current N-diheteroarylating agent

Sanjeev K. Verma, B. N. Acharya, Ramarao Ghorpade, Ajay Pratap, M. P. Kaushik

RSC ADVANCES (2013)

Article Multidisciplinary Sciences

Development of nsP2 protease based cell free high throughput screening assay for evaluation of inhibitors against emerging Chikungunya virus

Amrita Saha, Badri Narayan Acharya, Raj Priya, Nagesh K. Tripathi, Ambuj Shrivastava, M. Kameswara Rao, Pooja Kesari, Manju Narwal, Shailly Tomar, Sameer S. Bhagyawant, Manmohan Parida, Paban Kumar Dash

SCIENTIFIC REPORTS (2018)

Article Chemistry, Multidisciplinary

Design and synthesis of muscarinic acetylcholine receptor (mAChR) antagonist: pharmacophore-based screening and structure-based optimization

RamaRao Ghorpade, Deo Kumar, Sabita Nayak, Badri Narayan Acharya

MONATSHEFTE FUR CHEMIE (2019)

Article Infectious Diseases

Pyriproxyfen treated surface exposure exhibits reproductive disruption in dengue vector Aedes aegypti

Kavita Yadav, Sunil Dhiman, B. N. Acharya, Rama Rao Ghorpade, Devanathan Sukumaran

PLOS NEGLECTED TROPICAL DISEASES (2019)

Article Chemistry, Multidisciplinary

Synthesis and muscarinic acetylcholine receptor (mAChR) antagonist activity of substituted piperazine-triazoles

Badri Narayan Acharya, RamaRao Ghorpade, Kshetra Pal Singh, Deo Kumar, Sabita Nayak

Summary: This study synthesized a series of piperazine-triazole derivatives and found that a molecule based on benzonitrile piperazine triazole scaffold showed good tissue relaxation and blocking activity on the neurotransmitter ACh in ex vivo experiment.

MONATSHEFTE FUR CHEMIE (2021)

Article Chemistry, Organic

Catalyst-free photo-induced aerobic radical synthesis of lactams from N-alkenyl trichloroacetamides in 2-methyltetrahydrofuran as the radical initiator under violet light

Faiza Diaba, Gisela Trenchs

Summary: The first violet light-mediated synthesis of gamma- and delta-lactams from N-alkenyl trichloroacetamides is reported in this paper. The reactions are conducted in tetrahydrofuran or 2-methyltetrahydrofuran as the sole solvent without catalysts or additives, under non-anhydrous conditions in an air atmosphere where the solvent serves as the radical initiator.

ORGANIC & BIOMOLECULAR CHEMISTRY (2024)

Article Chemistry, Organic

Synthesis of mixed phosphorotrithioates via thiol coupling with bis(diisopropylamino)chlorophosphine and sulphenyl chloride

Feroze Hussain, Sajjad Ahmed, Ashiq Hussain Padder, Qazi Naveed Ahmed

Summary: This study reports a novel and efficient one-pot synthesis method for mixed phosphorotrithioates, which does not require supplementary additives and shows broad applicability.

ORGANIC & BIOMOLECULAR CHEMISTRY (2024)

Article Chemistry, Organic

Catalyst-free assembly of a polyfunctionalized 1,2,4-triazole-fused N-heterocycle, 6-acylated pyrrolo[1,2-a][1,2,4]triazolo[5,1-c]pyrazine

Hyunjin Oh, Ikyon Kim

Summary: A new 1,2,4-triazole-pyrrolo[1,2-a]pyrazine hybrid system, 6-acylpyrrolo[1,2-a][1,2,4]triazolo[5,1-c]pyrazine, was synthesized using a catalyst-free method. This method involved sequential exposure of pyrrole-2-carbonitrile-derived substrates to DMF-DMA and acyl hydrazide, resulting in the formation of acylated pyrazine and 1,2,4-triazole rings, enabling the installation of various substituents at specific positions on the core skeleton.

ORGANIC & BIOMOLECULAR CHEMISTRY (2024)

Article Chemistry, Organic

Synthesis of sulfinamides via photocatalytic alkylation or arylation of sulfinylamine

Ming Yan, Si-fan Wang, Yong-po Zhang, Jin-zhong Zhao, Zhuo Tang, Guang-xun Li

Summary: Here we developed an efficient photocatalytic approach for the convenient preparation of sulfinamides. The reaction allows for the gram-scale preparation of sulfinamides and the one-pot synthesis of various sulfonyl amides.

ORGANIC & BIOMOLECULAR CHEMISTRY (2024)

Article Chemistry, Organic

Two distinct protocols for the synthesis of unsymmetrical 3,4-disubstituted maleimides based on transition-metal catalysts

Farzaneh Bandehali-Naeini, Zahra Tanbakouchian, Noushin Farajinia-Lehi, Nicolas Mayer, Morteza Shiri, Martin Breugst

Summary: Two tandem catalytic systems were developed for the synthesis of novel 3,4-disubstituted maleimides using the same Ugi adducts. Different maleimide structures can be synthesized using either Pd or Cu catalysis.

ORGANIC & BIOMOLECULAR CHEMISTRY (2024)

Article Chemistry, Organic

Conversion of amino-terephthalonitriles to multi-substituted single benzene fluorophores with utility in bioimaging

Tanya Raghava, Anjan Chattopadhyay, Subhadeep Banerjee, Nivedita Sarkar

Summary: Amine substitution of two ortho fluorine atoms of tetrafluoroterephthalonitrile through SNAr chemistry is easily achievable. But further fluorine substitution is only possible under forcing conditions, yielding valuable fluorophores for bioimaging.

ORGANIC & BIOMOLECULAR CHEMISTRY (2024)

Review Chemistry, Organic

Microbial alcohol dehydrogenases: recent developments and applications in asymmetric synthesis

Anju Chadha, Santosh Kumar Padhi, Selvaraj Stella, Sowmyalakshmi Venkataraman, Thangavelu Saravanan

Summary: Alcohol dehydrogenases are enzymes that use cofactors for oxidation or reduction reactions of alcohols or carbonyl compounds. They are utilized in green chemistry and have applications in the production of pharmaceuticals. Recombinant enzymes have solved the challenge of producing purified enzymes in large quantities. Engineered alcohol dehydrogenases have been used in asymmetric synthesis in industry. Various methods have been established for regenerating expensive cofactors to make the enzymatic process more efficient and economically viable.

ORGANIC & BIOMOLECULAR CHEMISTRY (2024)