F
Farhad Hatamjafari
Researcher at Islamic Azad University
Publications - 44
Citations - 291
Farhad Hatamjafari is an academic researcher from Islamic Azad University. The author has contributed to research in topics: Catalysis & One-pot synthesis. The author has an hindex of 8, co-authored 42 publications receiving 228 citations. Previous affiliations of Farhad Hatamjafari include Shahid Beheshti University.
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Journal ArticleDOI
Microwave Assisted Convenient One-Pot Synthesis of Coumarin Derivatives via Pechmann Condensation Catalyzed by FeF3 under Solvent-Free Conditions and Antimicrobial Activities of the Products
Vahid Vahabi,Farhad Hatamjafari +1 more
TL;DR: The proposed solvent-free microwave irradiation method using the environmentally friendly catalyst FeF3 offers the unique advantages of high yields, shorter reaction times, easy and quick isolation of the products, excellent chemoselectivity, and a one-pot, green synthesis.
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Multi-Component Reaction of Amines, Alkyl Propiolates, and Ninhydrin: An Efficient Protocol for the Synthesis of Tetrahydro-dihydroxy-oxoindeno[1,2-b]pyrrole Derivatives
TL;DR: In this paper, a protocol for the synthesis of tetrahydrodihydroxy-oxoindeno[1,2-b]pyrrole from simple primary amines, alkyl propiolates, and ninhydrin was developed.
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One-pot rapid and efficient synthesis of new spiro derivatives of 11H-indeno(1,2-b)quinoxalin-11-one, 6H-indeno(1,2-b)pyrido (3,2-e)pyrazin-6-one and isatin-based 2-pyrazolines
TL;DR: Some new spiro derivatives of 11H-indeno(1,2-b)quinoxalin-11-ones 1a-b and 6H- indeno(3,2 -e)pyrazin-6-one 6 and isatin 10 were synthesized by two different pathways to give spiro compounds in improved yields.
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Theoretical investigations on the HOMO–LUMO gap and global reactivity descriptor studies, natural bond orbital, and nucleus-independent chemical shifts analyses of 3-phenylbenzo[d]thiazole-2(3H)-imine and its para-substituted derivatives: Solvent and substituent effects
TL;DR: Natural bond orbital analysis, salvation, and substituent effects of electron-releasing (CH3, -OH) and electron-withdrawing (Cl, NO2, CF3) groups at para positions on the molecular structure of as discussed by the authors.
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Effect of the mechanical activation on size reduction of crystalline acetaminophen drug particles
Esmaeil Biazar,Ali Beitollahi,S Mehdi Rezayat,Tahmineh Forati,Azadeh Asefnejad,Mehdi Rahimi,Reza Zeinali,Mahmoud Ardeshir,Farhad Hatamjafari,Ali Sahebalzamani,Majid Heidari +10 more
TL;DR: The size reduction influence of the acetaminophen particles by mechanical activation using a dry ball mill showed the greatest reduction in size was after milling for 30 hours, which may offer new properties to drugs.