A. Majhi

发表

Synthesis of a novel coumarin derivative and its binding interaction with serum albumins

Sandip Paul, Raju Ghanti, P. S. Sardar, 2019, Chemistry of Heterocyclic Compounds.

An efficient and convenient protocol for the synthesis of quinoxalines and dihydropyrazines via cyclization–oxidation processes using HClO4·SiO2 as a heterogeneous recyclable catalyst ☆

B. Das, A. Majhi, Katta Venkateswarlu, 2007 .

A facile nuclear bromination of phenols and anilines using NBS in the presence of ammonium acetate as a catalyst

V. Siddaiah, B. Das, A. Majhi, 2007 .

Niobium(V) chloride‐catalyzed synthesis of α‐aminonitriles with simultaneous reaction of aldehydes, amines and trimethylsilyl cyanide

Sung Soo Kim, A. Majhi, H. Kim, 2008 .

TMEDA Catalyzed Henry (Nitroaldol) Reaction under Metal and Solvent-free Conditions

Sung Soo Kim, A. Majhi, S. T. Kadam, 2009 .

A review on DBU-mediated organic transformations

A. Al-Harrasi, T. K. Mohanta, A. Majhi, 2022, Green Chemistry Letters and Reviews.

Highly efficient, mild and chemo- and stereoselective synthesis of enaminones and enamino esters using silica supported perchloric acid under solvent-free conditions

Y. K. Rao, B. Sridhar, B. Das, 2006 .

An efficient chemo‐ and stereoselective synthesis of enaminones and enaminoesters using (bromodimethyl)sulfonium bromide under solvent‐free conditions

B. Das, A. Majhi, K. R. Reddy, 2008 .

Treatment of Baylis–Hillman adducts with triethyl orthoacetate in the presence of heterogeneous catalysts: a method for the stereoselective synthesis of two different types of trisubstituted alkenes

J. Banerjee, B. Das, A. Majhi, 2006 .

An efficient synthesis of 2-benzoxepines from Morita-Baylis-Hillman adducts using heterogeneous recyclable catalysts.

J. Banerjee, B. Das, A. Majhi, 2006, Chemical & pharmaceutical bulletin.

Rare-earth metal triflates catalyzed three-component coupling of aldehydes, ketones or ketoesters and benzyl carbamate: An efficient one-pot stereoselective synthesis of Cbz-protected β-amino carbonyl compounds☆

B. Das, A. Majhi, K. Suneel, 2007 .

One-pot Efficient Synthesis of Cbz-protected β-Amino Ketones: Three-component Coupling of Aldehydes, Ketones, and Benzyl Carbamate

B. Das, A. Majhi, K. R. Reddy, 2007 .

A Facile Zn-mediated Stereoselective Synthesis of (E)- and (Z)-Trisubstituted Alkenes from Baylis–Hillman Adducts in Water and Its Application

J. Banerjee, B. Das, A. Majhi, 2006 .

Remarkably chemoselective reduction of unmodified baylis-hillman adducts by InCl3/NaBH4 : Application to the stereoselective synthesis of trisubstituted alkenones including two alarm pheromones

J. Banerjee, B. Das, A. Majhi, 2006 .

Solvent-free synthesis of α-aminonitriles from aldehydes, amines and trimethylsilyl cyanide catalyzed by thallium(III) chloride tetrahydrate

Sung Soo Kim, A. Majhi, S. T. Kadam, 2008 .

Rhodium(III) iodide hydrate catalyzed three-component coupling reaction : synthesis of α-aminonitriles from aldehydes, amines, and trimethylsilyl cyanide

Sung Soo Kim, A. Majhi, S. T. Kadam, 2008 .

Design, Synthesis, and Biophysical Studies of Novel 1,2,3-Triazole-Based Quinoline and Coumarin Compounds

Sandip Paul, A. Majhi, Pritam Roy, 2019, ACS Omega.

Rhodium(III) Iodide Hydrate Catalyzed Three‐Component Coupling Reaction: Synthesis of α‐Aminonitriles from Aldehydes, Amines, and Trimethylsilyl Cyanide.

Sung Soo Kim, A. Majhi, S. T. Kadam, 2008 .

A convenient highly stereoselective synthesis of allyl amides from Baylis–Hillman adducts using Amberlyst-15 as a heterogeneous reusable catalyst

J. Banerjee, B. Das, A. Majhi, 2006 .

A rapid and efficient stereoselective synthesis of (Z)- and (E)-allyl bromides from Baylis-hillman adducts using bromo (dimethyl )sulfonium bromide

M. Krishnaiah, B. Das, A. Majhi, 2006 .

Copper perchlorate hexahydrate: a highly efficient catalyst for the cyanosilylation of aldehydes

Sung Soo Kim, A. Majhi, H. Kim, 2008 .

I2–SiO2: An efficient heterogeneous catalyst for the Johnson–Claisen rearrangement of Baylis–Hillman adducts ☆

B. Das, A. Majhi, Katta Venkateswarlu, 2007 .

Organic reactions in water: an efficient zinc-mediated stereoselective synthesis of (E)- and (Z)-trisubstituted alkenes using unactivated alkyl halides.

J. Banerjee, B. Das, A. Majhi, 2004, Organic letters.

Novel Synthetic Methodologies. Part 156. An Efficient Chemo‐ and Stereoselective Synthesis of Enaminones and Enaminoesters Using (Bromodimethyl)sulfonium Bromide under Solvent‐Free Conditions.

B. Das, A. Majhi, K. R. Reddy, 2009 .

Fe3+-K-10 Montmorillonite Clay Catalyzed Friedel–Crafts Reaction of Unactivated Baylis–Hillman Adducts: An Efficient Stereoselective Synthesis of Trisubstituted Alkenes Containing a Benzyl Substituent

J. Banerjee, B. Das, A. Majhi, 2005 .

Synthetic applications of Baylis-Hillman chemistry: an efficient and solely stereoselective synthesis of (E)-alpha-methylcinnamic acids and potent hypolipidemic agent LK-903 from unmodified Baylis-Hillman adducts.

J. Banerjee, B. Das, A. Majhi, 2006, Chemical & pharmaceutical bulletin.

A facile one-pot stereoselective synthesis of trisubstituted (E)-2-methylalk-2-enoic acids from unactivated Baylis–Hillman adducts and a simple access to some important insect pheromones ☆

J. Banerjee, B. Das, A. Majhi, 2006 .

Synthetic Applications of the Baylis-Hillman Reaction: Simple and Convenient Synthesis of Five Important Insect Pheromones

J. Banerjee, B. Das, A. Majhi, 2006 .

Organic reactions in water : an efficient one-pot synthesis of acyloxiranes from Baylis-Hillman adducts using hypervalent iodine

B. Das, A. Majhi, Harish Holla, 2005 .

A highly efficient stereoselective synthesis of (Z)- and (E)-allyl iodides from Baylis–Hillman adducts ☆

J. Banerjee, B. Das, A. Majhi, 2005 .

An efficient stereoselective synthesis of (E)- and (Z)-trisubstituted alkenes from unactivated Baylis–Hillman adducts using NaBH4/CuCl2·2H2O

J. Banerjee, B. Das, A. Majhi, 2004 .

Addressing the Exigent Role of a Coumarin Fluorophore toward Finding the Suitable Microenvironment of Biomimicking and Biomolecular Systems: Steering to Project the Drug Designing and Drug Delivery Study

Sandip Paul, Soumen Ghosh, Sourav Das, 2021, ACS omega.

Interaction of serum albumins with fluorescent ligand 4-azido coumarin: spectroscopic analysis and molecular docking studies

Sandip Paul, S. Dasgupta, S. Sarkar, 2017 .

Studies on Novel Synthetic Methodologies. Part 74. An Efficient Synthesis of 2-Benzoxepines from Morita—Baylis—Hillman Adducts Using Heterogeneous Recyclable Catalysts.

J. Banerjee, B. Das, A. Majhi, 2006 .

Studies on Novel Synthetic Methodologies. Part 141. One-Pot Efficient Synthesis of Cbz-Protected β-Amino Ketones: Three-Component Coupling of Aldehydes, Ketones, and Benzyl Carbamate.

B. Das, A. Majhi, K. R. Reddy, 2008 .

Studies on Novel Synthetic Methodologies. Part 72. A Facile Zn‐Mediated Stereoselective Synthesis of (E)‐ and (Z)‐Trisubstituted Alkenes from Baylis—Hillman Adducts in Water and Its Application.

J. Banerjee, B. Das, A. Majhi, 2006 .

PKC Activation by Resveratrol Derivatives with Unsaturated Aliphatic Chain

J. Das, Satyabrata Pany, A. Majhi, 2012, PloS one.

Novel cytotoxic constituents of Orthosiphon diffusus

B. Sridhar, B. Das, A. Majhi, 2011 .

Molecular Imaging of Sirtuin1 Expression-Activity in Rat Brain Using Positron-Emission Tomography-Magnetic-Resonance Imaging with [18F]-2-Fluorobenzoylaminohexanoicanilide.

O. Muzik, T. Mangner, J. Gelovani, 2018, Journal of medicinal chemistry.

Binding of isoxazole and pyrazole derivatives of curcumin with the activator binding domain of novel protein kinase C.

J. Das, Satyabrata Pany, G. Rahman, 2011, Bioorganic & medicinal chemistry.

Novel Histone Deacetylase Class IIa Selective Substrate Radiotracers for PET Imaging of Epigenetic Regulation in the Brain

T. Mangner, G. Cisneros, J. Gelovani, 2015, PloS one.

Binding of curcumin and its long chain derivatives to the activator binding domain of novel protein kinase C.

J. Das, G. Rahman, A. Majhi, 2010, Bioorganic & medicinal chemistry.

Chemical modifications of resveratrol for improved protein kinase C alpha activity.

J. Das, Satyabrata Pany, A. Majhi, 2011, Bioorganic & medicinal chemistry.

Selective Modulation of Protein Kinase C α over Protein Kinase C ε by Curcumin and Its Derivatives in CHO-K1 Cells.

J. Das, Satyabrata Pany, A. Majhi, 2016, Biochemistry.

A waste valorization strategy for the synthesis of phenols from (hetero)arylboronic acids using pomegranate peel ash extract

A. Majhi, S. Avula, Jangam Lakshmidevi, 2022, Green Chemistry Letters and Reviews.

A new highly oxygenated pseudoguaianolide from a collection of the flowers of Parthenium hysterophorus.

Y. Tzeng, B. Das, Madamanchi Geethangili, 2005, Chemical & pharmaceutical bulletin.

Novel Synthetic Methodologies. Part 127. An Efficient and Convenient Protocol for the Synthesis of Quinoxalines and Dihydropyrazines via Cyclization—Oxidation Processes Using HClO4×SiO2 as a Heterogeneous Recyclable Catalyst.

B. Das, A. Majhi, Katta Venkateswarlu, 2007 .

Binding of isoxazole and pyrazole derivatives of curcumin with the activator binding domain of novel protein kinase C.

J. Das, Satyabrata Pany, G. Rahman, 2011, Bioorganic & medicinal chemistry.