Supported Cu(II)-Schiff base: novel heterogeneous catalyst with extremely high activity for eco-friendly, one-pot and multi-component C–S bond-forming reaction toward a wide range of thioethers as biologically active cores

2021 ◽  
Author(s):  
Pezhman Shiri ◽  
Ali Mohammad Amani ◽  
Jasem Aboonajmi
Keyword(s):  
Schiff Base ◽  
High Activity ◽  
Heterogeneous Catalyst ◽  
Biologically Active ◽  
One Pot ◽  
Bond Forming ◽  
Wide Range ◽  
Component C

Sulfated Tin Oxide: A Convenient Heterogeneous Catalyst for the Synthesis of 4-Arylmethylidene-3-substituted-isoxazol-5(4H)-ones

2021 ◽  
Vol 18 ◽  
Author(s):  
Nitishkumar S. Kaminwar ◽  
Sunil U. Tekale ◽  
Srinivas L. Nakkalwar ◽  
Rajendra P. Pawar
Keyword(s):  
Heterogeneous Catalyst ◽  
Tin Oxide ◽  
Heterocyclic Compounds ◽  
Biological Activities ◽  
Hydroxylamine Hydrochloride ◽  
One Pot ◽  
Easy Method ◽  
Three Component Reaction ◽  
Wide Range ◽  
The One

: Synthesis of isoxazole structural heterocyclic compounds is important due to their wide range of biological activities. In the present article, we report a convenient and easy method for the synthesis of 4-arylmethylidene-3-substituted-isoxazol-5(4H)-ones by the one-pot three-component reaction of aldehydes, β-keto ester, and hydroxylamine hydrochloride cat-alyzed by sulfated tin oxide as a heterogeneous catalyst.

A New Fluorescent Material of Mg (II) Complex with Salicylaldehyde- 4,4’-diaminodiphenylamine

2011 ◽  
Vol 366 ◽  
pp. 388-391
Author(s):  
Xi Shi Tai
Keyword(s):  
Schiff Base ◽  
Solid State ◽  
New Technologies ◽  
Luminescent Properties ◽  
Green Fluorescence ◽  
One Pot ◽  
Complex Material ◽  
Fluorescent Material ◽  
Wide Range ◽  
532 Nm

Novel schiff-base ligand and its Mg (II) complex were prepared by one-pot method after mixing salicylaldehyde, 4, 4’-Diaminodiphenylamine and MgCl2•6H2O. The luminescent properties of the Mg (II) complex material were investigated experimentally in solid state and in organic solvents. The results show that the Mg (II) complex material emits strong green fluorescence at 532 nm when excited at 393 nm even if the spit widths of excitation and emission are 2.5 nm, which may be applied as a potential fluorescent material in a wide range of new technologies.

Additive- and Oxidant-Free Expedient Synthesis of Benzimidazoles Catalyzed by Cobalt Nanocomposites on N-Doped Carbon

Synlett ◽  
2019 ◽  
Vol 30 (03) ◽  
pp. 319-324 ◽  
Author(s):  
Zhaozhan Wang ◽  
Tao Song ◽  
Yong Yang
Keyword(s):  
Functional Group ◽  
Direct Synthesis ◽  
Biologically Active ◽  
One Pot ◽  
Mild Conditions ◽  
Wide Range ◽  
High Yields

A one-pot direct synthesis of a wide range of biologically active benzimidazoles through coupling of phenylenediamines and aldehydes catalyzed by a highly recyclable nonnoble cobalt nanocomposite was developed. A broad set of benzimidazoles can be efficiently synthesized in high yields and with good functional-group tolerance under additive- and oxidant-free mild conditions. The catalyst can be easily recycled for successive uses, and the process permits gram-scale syntheses of benzimidazoles.

scholarly journals Screening of Biocatalysts for Synthesis of the Wieland–Miescher Ketone

Catalysts ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1063
Author(s):  
Mitul P. Patel ◽  
Nathaneal T. Green ◽  
Jacob K. Burch ◽  
Kimberly A. Kew ◽  
Robert M. Hughes
Keyword(s):  
Aqueous Media ◽  
Enantiomeric Excess ◽  
Biologically Active ◽  
Reaction Yield ◽  
Organic Transformations ◽  
One Pot ◽  
Enzyme Preparations ◽  
Wide Range ◽  
Important Intermediate ◽  
Optimized Conditions

Lipases, a versatile class of biocatalysts, have been shown to function in non-aqueous media/organic solvents and to possess “promiscuous” catalytic activity for a wide range of organic transformations. In this study, we explored the biocatalytic properties of a library of commercially available lipases by screening them for catalysis of a one-pot synthesis of Wieland–Miescher ketone, an important intermediate in the synthesis of biologically active compounds such as steroids and terpenoids, from methyl vinyl ketone and 2-methyl-1,3-cyclohexanedione. As a direct outgrowth of this screen, we created an optimized procedure for Wieland–Miescher ketone (WMK) synthesis using crude lipase preparations, characterizing both reaction yield and enantiomeric excess. We also identified principal components of the crude lipase mixture through proteomics and present evidence for a non-lipolytic origin of the observed catalysis. Finally, using the optimized conditions developed in this study, we propose a general absorbance-based screening methodology for assessing biocatalytic potential of crude enzyme preparations for synthesis of WMK.

Multi-Component One Pot assisted Synthesis, Anti-bacterial Capabilities and Scanning Electron Microscopy of Novel Corticosteroid Thiopyran

2020 ◽  
Vol 17 ◽  
Author(s):  
Sultanat ◽  
Anam Ansari ◽  
Mohd Qamar ◽  
Shafiullah ◽  
Sartaj Tabassum ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Carbon Disulphide ◽  
Building Blocks ◽  
Biologically Active ◽  
Multicomponent Synthesis ◽  
One Pot ◽  
Polycyclic Compounds ◽  
Wide Range ◽  
Scanning Electron

Background: Corticosteroids are important group of polycyclic compounds having a wide range of pharmacological and physiological properties. Thiopyran derivatives are important building blocks of many biologically active compounds. Objective: Keeping in mind the wide range of application of corticosteroid and thiopyran, herein we intend to develop a simple and efficient strategy to synthesize steroidal thiopyran derivatives starting with different commercially available corticosteroid and study their biological property. Materials and Methods: To achieve our aim, we employed a one-pot multicomponent synthesis of steroidal thiopyran derivatives by the reaction of corticosteriods, malononitrile and carbon disulphide in presence of triethyl amine as a catalyst. Results and Discussion : An array of novel thiopyran compounds were obtained with the highest product yield using Et3N. Scanning electron microscopy analysis manifested agglomeration pertaining to brick - shaped crystals of corticosteroid thiopyran. Synthesized compound were also found to be active as antibacterial agents. Conclusion: We describe a facile one-pot multicomponent synthesis of corticosteroid thiopyran derivatives which are found to possess antibacterial activity. Excellent yields of the products, simple work-up, easily available starting materials and non-chromatographic purification are some main advantages of this protocol.

Synthesis of bis-spiropiperidines using nano-CuFe2O4@chitosan as a robust and retrievable heterogeneous catalyst

2017 ◽  
Vol 41 (7) ◽  
pp. 416-419 ◽  
Author(s):  
Javad Safaei-Ghomi ◽  
Mohammad Rasool Lashkari ◽  
Hossein Shahbazi-Alavi
Keyword(s):  
Heterogeneous Catalyst ◽  
Aromatic Amine ◽  
Room Temperature ◽  
Barbituric Acid ◽  
Catalyst Loading ◽  
Reaction Conditions ◽  
One Pot ◽  
Wide Range ◽  
One Pot Condensation

An efficient pseudo six-component synthesis of bis-spiropiperidines is described by one-pot condensation of formaldehyde, aromatic amine and dimedone or N,N-dimethyl-barbituric acid using nano-CuFe2O4@chitosan at room temperature. This method provides several advantages including mild reaction conditions, applicability to wide range of substrates, reusability of the catalyst and little catalyst loading.

Transition-Metal-Catalyzed Annulative Coupling Cascade for the Synthesis of 3-Methyleneisoindolin-1-ones

Synthesis ◽  
2020 ◽  
Vol 52 (06) ◽  
pp. 807-818 ◽  
Author(s):  
So Won Youn
Keyword(s):  
Transition Metal ◽  
Bond Formation ◽  
Short Review ◽  
Coupling Reactions ◽  
Cyclization Reactions ◽  
One Pot ◽  
Bond Forming ◽  
Wide Range ◽  
Transition Metal Catalyzed ◽  
Metal Catalyzed

This short review describes the recent progress made on transition-metal-catalyzed annulative couplings for the synthesis of 3-methyleneisoindolin-1-ones, which are useful intermediates for the synthesis of numerous alkaloids and can be often found in a wide range of natural products and pharmaceuticals. In particular, new one-pot multiple C–C/C–N bond-forming processes for the construction of the 5-methylenepyrrol-2-one nucleus of such compounds are summarized.1 Introduction2 Intramolecular Cyclization Reactions: C3–N or C3–C3a and C–C Bond Formation3 Intermolecular Annulative Coupling Reactions3.1 C3–C3a and C3–N Bond Formation3.2 C1–C7a and C3–N Bond Formation3.3 C1–C7a and C1–N Bond Formation3.4 C1–C7a, C1–N and C3–N Bond Formation3.5 C3–C3a, C1–C7a, C1–N and C3–N Bond Formation: A Pd-Catalyzed One-Pot Sonogashira Coupling–Carbonylation–Amination–Cyclization Cascade4 Conclusion

scholarly journals Direct C(sp2)–H alkylation of unactivated arenes enabled by photoinduced Pd catalysis

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Daeun Kim ◽  
Geun Seok Lee ◽  
Dongwook Kim ◽  
Soon Hyeok Hong
Keyword(s):  
Functional Group ◽  
Alkyl Halide ◽  
Alkyl Halides ◽  
Biologically Active ◽  
One Pot ◽  
Bond Forming ◽  
Alkyl Groups ◽  
Alkyl Bromides ◽  
Reaction Proceeds ◽  
Alkylation Reactions

AbstractDespite the fundamental importance of efficient and selective synthesis of widely useful alkylarenes, the direct catalytic C(sp2)–H alkylation of unactivated arenes with a readily available alkyl halide remains elusive. Here, we report the catalytic C(sp2)–H alkylation reactions of unactivated arenes with alkyl bromides via visible-light induced Pd catalysis. The reaction proceeds smoothly under mild conditions without any skeletal rearrangement of the alkyl groups. The direct syntheses of structurally diverse linear and branched alkylarenes, including the late-stage phenylation of biologically active molecules and an orthogonal one-pot sequential Pd-catalyzed C–C bond-forming reaction, are achieved with exclusive chemoselectivity and exceptional functional group tolerance. Comprehensive mechanistic investigations through a combination of experimental and computational methods reveal a distinguishable Pd(0)/Pd(I) redox catalytic cycle and the origin of the counter-intuitive reactivity differences among alkyl halides.

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