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Yogesh S. Munot
Researcher at National Taiwan Normal University
Publications - 10
Citations - 212
Yogesh S. Munot is an academic researcher from National Taiwan Normal University. The author has contributed to research in topics: Chemoselectivity & Catalysis. The author has an hindex of 5, co-authored 10 publications receiving 198 citations. Previous affiliations of Yogesh S. Munot include National Chemical Laboratory.
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Journal ArticleDOI
Direct atom-efficient esterification between carboxylic acids and alcohols catalyzed by amphoteric, water-tolerant TiO(acac)2.
Chien-Tien Chen,Yogesh S. Munot +1 more
TL;DR: The new neutral catalytic protocol with the optimal TiO(acac)2 tolerates many stereo/electronic structural variations in both ( di)acid and (di)alcohol components with high chemoselectivity.
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Nucleophilic Acyl Substitutions of Anhydrides with Protic Nucleophiles Catalyzed by Amphoteric, Oxomolybdenum Species
Chien-Tien Chen,Jen-Huang Kuo,Vijay D. Pawar,Yogesh S. Munot,Shieu-Shien Weng,Cheng-Hsiu Ku,Cheng-Yuan Liu +6 more
TL;DR: The amphoteric character of the Mo=O unit in oxomolybdenum chlorides was found to be responsible for the catalytic NAS profile as supported by a control NAS reaction of using an authentic adduct-MoOCl(2)(O( 2)CBu(t)())(2) between pivalic anhydride and MoO(2)Cl(1) as the catalyst.
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Diethylene glycol ether-linked 3,4,5-trihydroxybenzamides as triply branched dendritic anchors to CdSe/ZnS core/shell type nanoparticles: potential hydrophilic fluorescent probes.
TL;DR: Functionalized N-2-mercaptoethyl-gallamides bearing three or five hydroxyl units that are tethered with diethylene glycol ether(s) allow for transferring hydrophobically pyridine-capped CdSe/ZnS core/shell nanoparticles from an organic to an aqueous layer with intact fluorescent profiles.
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Transesterification of α-haloesters and β-ketoesters over Mg-Al-hydrotalcites (HT)-like anionic clays
Vivek J. Bulbule,Hanumant B. Borate,Yogesh S. Munot,Vishnu H. Deshpande,Sangmeshwer P. Sawargave,A. G. Gaikwad +5 more
TL;DR: Transesterification of α-haloesters was achieved by reaction of alcohols in the presence of Mg–Al-HT-like anionic clays and β-Ketoesters were also transesterified under similar conditions on reaction with alcohols with a wide variety of functional groups.
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Simple Synthesis of Two Naphthoquinone Antibiotics Psychorubrin and Pentalongin
TL;DR: In this article, 1H-Naphtho[2,3-c]pyran derivatives were synthesized using chloromethylation of substituted 2-naphthylacetic acid as the key step.