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Yernaidu Reddi

Researcher at Indian Institute of Technology Bombay

Publications -  18
Citations -  507

Yernaidu Reddi is an academic researcher from Indian Institute of Technology Bombay. The author has contributed to research in topics: Medicine & Enantioselective synthesis. The author has an hindex of 10, co-authored 13 publications receiving 307 citations. Previous affiliations of Yernaidu Reddi include University of Minnesota.

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Mechanistic Insights on Orthogonal Selectivity in Heterocycle Synthesis

TL;DR: In this article, a method for catalytic regioselective synthesis of benzofurans starting from phenols was developed, where the choice of reacting partner, olefin versus α,β-unsaturated acid, is critical to dictate the isomeric product formation.
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A phosphomide based PNP ligand, 2,6-{Ph2PC(O)}2(C5H3N), showing PP, PNP and PNO coordination modes

TL;DR: A new class of PNP pincer ligands, pyridine-2, 6-diylbis(diphenylphosphino)methanone, 2,6-{Ph2PC(O)}2(C5H3N) (hereafter referred to as "bis(phosphomide)"), was prepared by the reaction of picolinoyldichloride with diphenyl phosphine in the presence of triethylamine.
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Modeling the mechanism of CO2/cyclohexene oxide copolymerization catalyzed by chiral zinc β-diiminates: factors affecting reactivity and isotacticity

TL;DR: Using density functional theory, the authors in this article used copolymerization of CO2 and cyclohexene oxide (CHO) upcycles CO2 into value-added, chemically recyclable, thermoplastic poly(cyclohexenes carbonate) (PCHC).
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Diels–Alder/Ene Reactivities of 2-(1′-Cycloalkenyl)thiophenes and 2-(1′-Cycloalkenyl)benzo[b]thiophenes with N-Phenylmaleimides: Role of Cycloalkene Ring Size on Benzothiophene and Dibenzothiophene Product Distributions

TL;DR: 2D NMR studies indicate that the isolated isomers for 2-(1´-cycloalkenyl)thiophenes having five-, six-, and seven-membered rings are aromatized benzothiophene products whereas, eight- and twelve-members rings are un-rearranged adducts.
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Stereoregular functionalized polysaccharides via cationic ring-opening polymerization of biomass-derived levoglucosan

TL;DR: The facile synthesis and characterization of 1,6-α linked functional stereoregular polysaccharides from biomass-derived levoglucosan via cationic ring-opening polymerization (cROP) are reported.