P
Palakodety Radha Krishna
Researcher at Indian Institute of Chemical Technology
Publications - 118
Citations - 1263
Palakodety Radha Krishna is an academic researcher from Indian Institute of Chemical Technology. The author has contributed to research in topics: Total synthesis & Baylis–Hillman reaction. The author has an hindex of 17, co-authored 118 publications receiving 1218 citations. Previous affiliations of Palakodety Radha Krishna include Russian Academy of Sciences.
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Recent advances and applications in asymmetric aza-Michael addition chemistry
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A versatile and practical synthesis of bis(indolyl)methanes/bis(indolyl)glycoconjugates catalyzed by trichloro-1,3,5-triazine☆
TL;DR: In this paper, a practical and efficient electrophilic substitution reaction of indoles with a variety of aldehydes was carried out using catalytic trichloro-1,3,5-triazine (10−mol%) in acetonitrile to furnish the corresponding bis(indolyl)methanes in excellent yields.
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‘In situ’ Generated ‘HCl’ - An Efficient Catalyst for Solvent-Free Hantzsch Reaction at Room Temperature: Synthesis of New Dihydropyridine Glycoconjugates
TL;DR: HCl, generated in situ from 2,4,6-trichloro[1,3,5]triazine (TCT, cyanuric chloride), catalyzed a solvent free Hantzsch reaction at room temperature with enhanced reaction rates, allowing facile preparation of glycoconjugates of dihydropyridines under mild reaction conditions in high yields.
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2-Azidoethyl glycosides: glycosides potentially useful for the preparation of neoglycoconjugates
Anatoly Ya. Chernyak,Gangavaram V. M. Sharma,Leonid O. Kononov,Palakodety Radha Krishna,Anatoly B. Levinsky,Nikolay K. Kochetkov,Alla V. Rama Rao +6 more
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Zirconium(IV) chloride catalyzed new and efficient protocol for the selective cleavage of p-methoxybenzyl ethers.
TL;DR: A highly selective and efficient method for the unmasking of p-methoxybenzyl (PMB) ethers and esters has been developed by use of 20 mol % of zirconium(IV) chloride as Lewis acid in acetonitrile.