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Dilip V. Jarikote
Researcher at National University of Ireland, Galway
Publications - 32
Citations - 1393
Dilip V. Jarikote is an academic researcher from National University of Ireland, Galway. The author has contributed to research in topics: Ionic liquid & Catalysis. The author has an hindex of 16, co-authored 31 publications receiving 1319 citations. Previous affiliations of Dilip V. Jarikote include National Chemical Laboratory & Humboldt University of Berlin.
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Forced intercalation probes (FIT Probes): thiazole orange as a fluorescent base in peptide nucleic acids for homogeneous single-nucleotide-polymorphism detection.
TL;DR: New peptide nucleic acid (PNA) based probes are described in which the intercalator dye thiazole orange (TO) serves as a base surrogate, and the emission of TO‐containing PNA probes is attenuated when forced to intercalate next to a mismatched base pair.
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Ultrasound promoted Suzuki cross-coupling reactions in ionic liquid at ambient conditions.
TL;DR: Palladium catalyzed Suzuki cross-coupling reactions of halobenzenes including chlorobenzees with phenylboronic acid have been achieved at ambient temperature in the absence of a phosphine ligand using the ionic liquid 1,3-di-n-butylimidazolium tetrafluoroborate with methanol as co-solvent under ultrasonic irradiation.
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Room temperature ionic liquid promoted synthesis of 1,5-benzodiazepine derivatives under ambient conditions
Dilip V. Jarikote,S. A. Siddiqui,R. Rajagopal,Thomas Daniel,Rajgopal J. Lahoti,K. V. Srinivasan +5 more
TL;DR: The reaction of o-phenylenediamines with both acyclic and cyclic ketones in the ionic liquid 1,3-di-n-butylimidazolium bromide afforded 1,5-benzodiazepines in excellent isolated yields in the absence of a catalyst at ambient temperature as discussed by the authors.
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Knoevenagel condensation reactions in an ionic liquid
TL;DR: In this paper, the condensation reaction of 4-oxo-(4H)-1-benzopyran-3-carbaldehydes and of aromatic aldehydes with 3-methyl-1-phenylpyrazolin-5-4H-one were carried out in an ionic liquid, ethylammonium nitrate, at room temperature in shorter times with higher yields of 78−92 and 70−75%, respectively, than found using conventional procedures.
Journal ArticleDOI
FIT probes: peptide nucleic acid probes with a fluorescent base surrogate enable real-time DNA quantification and single nucleotide polymorphism discovery.
TL;DR: The use of d-ornithine rather than aminoethylglycine as the PNA backbone increases the intensity of fluorescence emitted by matched probe-target duplexes while specificity offluorescence signaling under nonstringent conditions is also increased.