Search Results - "Rajana, Nagaraju"
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Development and Validation of Miglitol and Its Impurities by RP-HPLC and Characterization Using Mass Spectrometry Techniques
Published in Scientia pharmaceutica (14-10-2016)“…Alpha glucoside inhibitors used to treat type-2 diabetes mellitus (DM) are likely to be safe and effective. These agents are most effective for postprandial…”
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Identification, method development, validation, and characterization of Aza sugars by an ion-chromatography, high-resolution mass spectrometer, and LC-MS/MS
Published in Journal of analytical science and technology (24-01-2018)“…Background Aza sugars are organi c sugars having nitrogen containing polyhydroxyl sugar molecules. These molecules are active pharmaceutical ingredients; these…”
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Novel cocrystals of brexpiprazole with improved solubility
Published in Journal of crystal growth (01-12-2020)“…[Display omitted] •Prepared novel cocrystals of brexpiprazole with biologically acceptable coformers.•All the cocrystals were completely characterized by PXRD,…”
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4
Formal synthesis of Cladospolide C &epi-Cladospolide C using R-(+)-γ-valerolactone as a chiral synthon
Published in Tetrahedron (10-05-2019)“…The formal synthesis of Cladospolide-C and its analog is achieved by using enantiopure (R)-γ–valerolactone 10. The significant points of this synthesis are the…”
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Characterization of Five Oxidative Degradation Impurities and One Process Impurity of Suvorexant Drug Substance by LC-MS/MS, HR-MS and 1D, 2D NMR: Validation of Suvorexant Drug Substance and Process Impurities by HPLC and UPLC
Published in Journal of chromatographic science (25-04-2020)“…Abstract During the oxidative (10% H2O2) degradation of suvorexant drug substance, around 1.0% of one impurity and less than 1.0% four impurities were found by…”
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Inside Front Cover: Reversed‐phase chiral high‐performance liquid chromatography method for separation of abacavir sulfate enantiomer in drug substance
Published in Separation science plus (01-11-2020)“…DOI: 10.1002/sscp.202000080 The cover picture shows the development, optimization and validation of Reversed phase chiral HPLC method for separation of…”
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An Orthogonal Approach for Determination of Acetamide Content in Pharmaceutical Drug Substance and Base-Contaminated Acetonitrile by GC and GC-MS External Method
Published in Journal of chromatographic science (17-10-2019)“…Acetamide is a potential genotoxic impurity; it should control in drug substance based on daily dosage level. It forms from base-contaminated acetonitrile and…”
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A short diastereoselective synthesis of cis-(2S,4S) and cis-(2R,4R)-4-hydroxyprolines
Published in Tetrahedron letters (10-06-2015)“…[Display omitted] A concise synthesis of (2R,4R)-4-hydroxyproline (1) and (2S,4S)-4-hydroxyproline (2) has been developed in enantiomerically pure form from…”
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Back Cover: Development and validation of HPLC methodology for quantitative estimation of Efinaconazole in topical pharmaceutical formulation prepared in‐house for the treatment of onychomycosis
Published in Separation science plus (01-10-2020)“…DOI: 10.1002/sscp.202000050 The cover picture shows an orthogonal approach for method development and validation of three potential halo alkyl alcohol…”
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An orthogonal approach for method development and validation of three potential halo alkyl alcohol genotoxic impurities in miglitol drug substance by fast gas chromatography–mass spectrometry
Published in Separation science plus (01-10-2020)“…Miglitol is an azasugar. It is the oral antidiabetic drug that inhibits the glucose generation from the polysaccharides and oligosaccharides. The miglitol…”
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Reversed‐phase chiral high‐performance liquid chromatography method for separation of abacavir sulfate enantiomer in drug substance
Published in Separation science plus (01-11-2020)“…For separation of abacavir sulfate enantiomers, normal phase chiral methods were reported. Handling of normal phase solvents for high‐performance liquid…”
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12
Diversity oriented concise asymmetric synthesis of azasugars: a facile access to l-2,3-trans-3,4-cis-dihydroxyproline and (3S,5S)-3,4,5-trihydroxypiperidine
Published in Tetrahedron letters (02-12-2015)“…[Display omitted] Diversity oriented concise asymmetric syntheses of l-2,3-trans-3,4-cis-dihydroxyproline and (3S,5S)-3,4,5-trihydroxypiperidine have been…”
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Concise and highly stereoselective syntheses of d-fagomine and 2-epi-fagomine
Published in Tetrahedron letters (23-03-2016)“…[Display omitted] Highly stereoselective total syntheses of polyhydroxylated piperidines d-fagomine and 2-epi-fagomine have been developed starting from…”
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Quantitative method for determination of 3,3‐dimethylallyl bromide genotoxic impurity in Tazarotene drug substance by GC‐MS
Published in Separation science plus (01-09-2020)“…A highly sensitive gas chromatography‐mass spectrometry quantitative method was developed for 3,3‐dimethylallyl bromide genotoxic impurity in the tazarotene…”
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Diastereoselective total synthesis of piperidine alkaloids: (2R,5R)-5-hydroxyhomopipecolic acid and (2R,5R,8R)-5-hydroxysedamine
Published in Tetrahedron letters (22-04-2015)“…[Display omitted] Total synthesis of 2,5-disubstituted piperidine alkaloids, 5-hydroxyhomopipecolic acid (1) and 5-hydroxysedamine (2) was accomplished in…”
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A concise stereoselective synthesis of (+)-1-deoxy-6-epi-castanospermine
Published in Tetrahedron letters (30-03-2016)“…[Display omitted] •The stereoselective imine reduction was achieved by using sodium cyanoborohydride.•Mitsunobu cyclization selectively with primary…”
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