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Gurpinder Singh

Researcher at Guru Nanak Dev University

Publications -  18
Citations -  250

Gurpinder Singh is an academic researcher from Guru Nanak Dev University. The author has contributed to research in topics: Nitrone & Chemistry. The author has an hindex of 7, co-authored 15 publications receiving 224 citations.

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Design, synthesis, and evaluation of novel 6-chloro-/fluorochromone derivatives as potential topoisomerase inhibitor anticancer agents.

TL;DR: The compounds displayed promising anticancer activity under these test systems and shall serve as useful 'leads' for further design.
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Evaluation of intrabony defects treated with platelet-rich fibrin or autogenous bone graft: A comparative analysis.

TL;DR: The bivariate correlation results revealed that any of the two radiographic techniques (IOPA and OPG) can be used for analysis of the regenerative therapy in IBDs.
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Unusual conversion of substituted-3-formylchromones to 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones: a facile and efficient route to novel 1,2,4-dithiazoles

TL;DR: Substituted 3-formylchromones react with 2-phenyl-4-dimethylamino-1-thia-3-azabuta-1,3-diene ( 4 ) or thio-benzamide ( 7 ) by heating their toluene solution in a sealed tube to give novel substituted 3-(5phenyl)-3 H -[1,2,4]dithiazol-3yl)chromen-4ones ( 6a − e ) in high yields as discussed by the authors.
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Intramolecular low-temperature 1,3-dipolar cycloadditions of nitrones: synthesis of chromano-heterocycles

TL;DR: In contrast to the reported facile intramolecular 1,3-dipolar cycloadditions of in-situ generated nitrone on heterocyclic systems, reactions of 2-(N-allyl/crotyl/cinnamyl-anilino)-3-formylchromones with N-phenyl-/methylhydroxylamine under comparable conditions, afford fused isoxazolidines only in low to moderate yields; the corresponding amides derived from rearrangement of in situ generated nitrones are formed as major products RE
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Synthesis and cytotoxic evaluation of substituted 3-(3′-indolyl-/3′-pyridyl)-isoxazolidines and bis-indoles

TL;DR: In this article, a stereoselective 1,3-dipolar cycloadditions of C -(3-indolyl)- N -phenylnitrone (10) with different mono-substituted, disubstitized and cyclic dipolarophiles under mono-mode microwave irradiation were carried out to obtain substituted 3-(indol-3′-3-yl)- N-phenyl-isoxazolidines (16−22).