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Karangula Jyothi

Researcher at Indian Institute of Chemical Technology

Publications -  15
Citations -  325

Karangula Jyothi is an academic researcher from Indian Institute of Chemical Technology. The author has contributed to research in topics: Dihydroxylation & Catalysis. The author has an hindex of 9, co-authored 15 publications receiving 313 citations.

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Catalytic asymmetric dihydroxylation of olefins with reusable OsO(4)(2-) on ion-exchangers: the scope and reactivity using various cooxidants.

TL;DR: In this article, the authors evaluated the performance of two different types of catalysts for asymmetric dihydroxylation of trans-stilbene, namely, Resin-OsO 4 and SiO 2 -OsO4, and showed consistent activity and enantioselectivity in asymmetric diolation using K 3 Fe(CN) 6 and molecular oxygen as cooxidants.
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A new bifunctional catalyst for tandem Heck–asymmetric dihydroxylation of olefins

TL;DR: In this paper, a new bifunctional catalyst consisting of active palladium and osmium species anchored on silica gel through a mercaptopropyl spacer and a cinchona alkaloid respectively has been prepared for the first time and used in the heterogeneous tandem Heck-asymmetric dihydroxylation of olefins to afford diols with excellent yields and enantiomeric excesses.
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Bifunctional catalysts stabilized on nanocrystalline magnesium oxide for one-pot synthesis of chiral diols

TL;DR: In this article, a bifunctional catalysts composed of PdCl 4 2-, OsO 4 2 -, O4 2 - and O4 O 2 -Na 2 WO 4 with nanocrystalline MgO were proposed.
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Achiral Dihydroxylation of Olefins by Osmate (OsO42−) Stabilised on Nanocrystalline Magnesium Oxide

TL;DR: In this paper, a recoverable and reusable new heterogeneous AP-Mg-OsO4 catalyst was designed and developed for the first time via a counterionic stabilisation of OsO42- with Mg2+ present on the corner or edge of nanocrystalline MgO.
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Allylation of aldehydes, aldimines and ring opening of terminal aromatic epoxides by scandium triflate using polyethylene glycol (PEG) as an efficient recyclable medium

TL;DR: The PEG-scandium triflate catalyzed allylation of a variety of aldehydes and aldimines using polyethylene glycol (PEG) as a recyclable reaction medium proceeds smoothly and affords corresponding homoallylic alcohols and amines in good yields as mentioned in this paper.