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Parag S. Roy

Researcher at University of North Bengal

Publications -  27
Citations -  88

Parag S. Roy is an academic researcher from University of North Bengal. The author has contributed to research in topics: Pterin & Chemistry. The author has an hindex of 5, co-authored 22 publications receiving 76 citations.

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Coordination chemistry of f-block elements with imine acids. Part IV. Synthetic and chiroptical studies on lanthanide(III) complexes of imine acids derived from L-alanine, L-valine, L-tyrosine and L-glutamic acid

TL;DR: In this article, the dominant conformers were determined from c.h n.m.d. spectra supported by 1H n.r. data, except for the L-glutamic acid derived complexes which were insoluble.
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Studies on the different forms of some mixed chelate complexes of dioxouranium(VI) with cupferron

TL;DR: In this paper, a series of mixed chelate complexes of identical composition of the type (NH4)2[UO2(L)2B] and (NH 4]2 [UO 2(L 2B] 2X2] have been thoroughly characterised through elemental analysis, conductance data, X-ray, IR, electronic, NMR spectra as well as thermogravimetric and differential thermal analyses.
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Synthesis, chiroptical and electrochemical studies of dioxouranium(VI) complexes of aldimine derivatives of L-/D-histidine and crystal structure of (2,2′-bipyridyl)dioxo(N-o-vanillylidene-L-histidinato)uranium(VI)–water–methanol(1/1/1)

TL;DR: In this article, a series of new dioxouranium(VI) complexes has been synthesized using N-(salicylidene)-L-histidine (H2sal-Lhis) and N-(o-vanillylidenes)-L -histidine(H2van-L-his), and corresponding D-histidines.
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Studies on 8-quinolinol-5-sulphonic acid complexes of dioxouranium(VI) and elucidation of their structures and bondings through physico-chemical analyses

TL;DR: In this paper, the uranyl ion and 8-quinolinol-5-sulphonic acid have been studied and the soluble free acid with balancing secondary cations M 3 (I)H[UO 2 X 3 ] · x H 2 O (where M (I)) = Na +, K + ; X = (C 9 H 5 NSO 4 ) 2− ; x = 0.5, 1) has been isolated in the solid state.
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Investigating the Role of the Reduced Solubility of the Pirfenidone-Fumaric Acid Cocrystal in Sustaining the Release Rate from Its Tablet Dosage Form by Conducting Comparative Bioavailability Study in Healthy Human Volunteers.

TL;DR: The present study suggests that cocrystallization offers a promising strategy to reduce the solubility of PFD and opens the door for potential new dosage forms of this important pharmaceutical.