Anindita Sarkar

ORCID: 0009-0004-0708-8882
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About
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Research Areas
  • Crystal structures of chemical compounds
  • Catalytic C–H Functionalization Methods
  • Vanadium and Halogenation Chemistry
  • Radical Photochemical Reactions
  • Polyoxometalates: Synthesis and Applications
  • Crystallography and molecular interactions
  • Metal-Catalyzed Oxygenation Mechanisms
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Organophosphorus compounds synthesis
  • Molecular Sensors and Ion Detection
  • Asymmetric Hydrogenation and Catalysis
  • Herpesvirus Infections and Treatments
  • Cytomegalovirus and herpesvirus research
  • Organometallic Compounds Synthesis and Characterization
  • Axial and Atropisomeric Chirality Synthesis
  • Metal complexes synthesis and properties
  • Hepatitis C virus research
  • Sulfur-Based Synthesis Techniques
  • Crystallization and Solubility Studies
  • Advanced Chemical Sensor Technologies
  • Catalytic Alkyne Reactions
  • Synthetic Organic Chemistry Methods
  • Analytical chemistry methods development
  • Synthesis and Catalytic Reactions
  • Water Treatment and Disinfection

United States Pharmacopeial Convention
2024

University of Calcutta
2024

Western University
2014

University of Pretoria
2011

University of Hyderabad
2006-2009

Abstract Ru(II)‐catalyzed and solvent‐switched [3+2]‐spiroannulation [4+n] (n=1, 2, 3) annulations of 2‐aryl quinazolinone or 2‐aryl‐2,3‐dihydrophthalazine‐1,4‐diones with ynones alkynyl alcohol 1,3‐diynes under mild reaction conditions have been analyzed. These reactions take place in the presence appropriate solvent features a redox‐neutral pathway. Ynone serves as an ‘atypical one‐carbon unit’ [4+1] annulation generates tetrasubstituted carbon center bearing diverse heterocycles through...

10.1002/adsc.202301277 article EN Advanced Synthesis & Catalysis 2024-02-21

Abstract In an acetonitrile/water mixture, reactions of the N , ′‐bis(diacetyl)hydrazine (H 2 diah), bis(acetylacetonato)oxidovanadium(IV) [VO(acac) ] and monodentate ‐coordinating heterocycles (hc) in a 1:2:2 mol ratio provide yellow divanadium(V) complexes formula [(hc)O V(μ‐diah)VO (hc)] ( 1 hc = imidazole; pyrazole; 3 3,5‐dimethyl pyrazole). On other hand, same solvent mixture reagents 1:4:2 produce green linear tetravanadium(IV,V,V,IV) [(acac) OV(μ‐O)VO(hc)(μ‐diah)(hc)OV(μ‐O)VO(acac) 4...

10.1002/ejic.200900680 article EN European Journal of Inorganic Chemistry 2009-10-29

Two structurally distinct and biologically privileged succinimide isoindole heteroarenes bearing benzothiadiazinedioxide motif-centered hybrid conjugates are proficiently achieved through Rh(III)-catalyzed sequential C(sp

10.1021/acs.joc.4c00366 article EN The Journal of Organic Chemistry 2024-05-17

In the title compound, 3C(12)H(24)N(+)·C(5)H(7)N(2)O(7)P(2) (3-)·C(2)H(6)O·H(2)O, zoledronic acid mol-ecule is singly protonated and stabilized by an intra-molecular O-H⋯O inter-action. The three-dimensional crystal structure inter-molecular O-H⋯O, O-H⋯N N-H⋯O inter-actions. ethanol solvent disordered over two positions; site-occupancy factor of major component 0.510 (4).

10.1107/s1600536811042206 article EN cc-by Acta Crystallographica Section E Structure Reports Online 2011-10-21

Distinctive, green, innovative, and well-organized photoinduced (metal- or photocatalyst-free) regioselective decarbonylative decarboxylative C–O bond functionalization protocols to access aryl 2-aminobenzoates 2-substituted benzoxazinone derivatives in excellent yields have been devised. These are achieved through the chemoselective scission of isatoic anhydride with ketones, diaryliodonium triflate, nitroalkene, phthalazinone, phenol derivatives, which, turn, served as representative...

10.1021/acs.joc.4c01856 article EN The Journal of Organic Chemistry 2024-12-05

The present article provides a novel technique for the co-amorphous formation of acyclovir and oxalic acid as an excipient. Designated ACV-oxalic acid, methods preparation thereof its use in pharmaceutical applications are described. was characterized by powder X-ray diffraction, differential scanning calorimetry thermogravimetric analysis. Stability with respect to relative humidity (RH) evaluated compared parent ACV. aqueous solubility significantly improved (about 8 times more soluble) at...

10.21065/1920-4159.1000251 article EN Journal of Applied Pharmacy 2017-01-01

In the title compound, C(4)H(14)N(2) (2+)·2C(7)H(5)O(3) (-), both N,N-dimethyl-ethylenediamine N atoms are protonated and two 3-hy-droxy-benzoate anions act as counter-ions. crystal, cations linked by a network of N-H⋯O O-H⋯O hydrogen bonds.

10.1107/s1600536811040578 article EN cc-by Acta Crystallographica Section E Structure Reports Online 2011-10-07
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