M
Murlidhar S. Shingare
Researcher at Dr. Babasaheb Ambedkar Marathwada University
Publications - 230
Citations - 3152
Murlidhar S. Shingare is an academic researcher from Dr. Babasaheb Ambedkar Marathwada University. The author has contributed to research in topics: Catalysis & Ionic liquid. The author has an hindex of 28, co-authored 230 publications receiving 2887 citations. Previous affiliations of Murlidhar S. Shingare include Shivaji College, Karwar.
Papers
More filters
Journal ArticleDOI
β-Cyclodextrin-SO3H-catalyzed facile and highly efficient synthesis of 4-thiazolidinones under solvent free conditions
Mahendra A. Chaudhari,Jitendra B. Gujar,Deepak S. Kawade,Pravin V. Shinde,Murlidhar S. Shingare +4 more
TL;DR: In this article, a one-pot, multi-component, green, and highly efficient procedure has been developed for synthesis of 4-thiazolidinones, using β-cyclodextrin-SO3H as an eco-friendly and recyclable catalyst.
Journal ArticleDOI
An Efficient One-Pot Strategies for the Synthesis of [1,3] Oxazine Derivatives
TL;DR: In this paper, a phase transfer catalyst (PTC) was used as a mild reaction promoter for the cyclocondensation of formalin, β-naphthol and aromatic amines to afford respective 2,3-dihydro-2-phenyl-1H-Naphtho-[1,2-e] [1,3] oxazine derivatives.
Journal ArticleDOI
Synthesis of 2-aryl-1-arylmethyl-1H-benzimidazoles using chlorosulfonic acid at room temperature
TL;DR: Chlorosulfonic acid (ClSO 3 H) used to be a catalyst for the synthesis of 2-aryl-1-arylmethyl-1 H -benzimidazoles which was efficiently simple and convenient as mentioned in this paper.
Journal ArticleDOI
N-donor Ligand as Catalyst : A Simple Aza-Michael Addition Reaction in Aqueous Media
TL;DR: In this article, a novel approach for the Aza-Michael addition reactions between various amines and α,β-unsaturated esters, nitriles and ketones using N-donor Ligand catalyst (3 mol %) is described.
Journal ArticleDOI
An efficient method for the N-arylation of phenylurea via copper catalyzed amidation
Sandip N. Gavade,Ravi S. Balaskar,Madhav S. Mane,Pramod N. Pabrekar,Murlidhar S. Shingare,Dhananjay V. Mane +5 more
TL;DR: The coupling reaction of phenylurea with different functionalized aryl halides in the presence of air stable CuI, N, N -dimethylethylenediamine as a ligand, and K 3 PO 4 as a base gives symmetrical and unsymmetrical diarylureas in relatively high yields.