Search Results - "Gilla, Goverdhan"
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Application of [3 + 2]-Cycloaddition in the Synthesis of Valdecoxib
Published in Synthetic communications (01-03-2012)“…A large scale synthesis of valdecoxib 1 is described. Our work features potential application of [3 + 2]-dipolar cycloaddition involving enamine and in…”
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2
An Improved and Scalable Process for Celecoxib: A Selective Cyclooxygenase-2 Inhibitor
Published in Organic process research & development (16-01-2009)“…An improved, scalable and commercially viable process is developed for an active pharmaceutical ingredient, celecoxib…”
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3
Synthesis and characterization of critical process related impurities of an asthma drug – Zafirlukast
Published in Journal of Saudi Chemical Society (01-04-2014)“…Zafirlukast is an oral leukotriene receptor antagonist (LTRA) for the treatment of pulmonary disorders such as asthma. During the process development of…”
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4
Novel solid form of prothioconazole and its crystallographic analysis
Published in Journal of molecular structure (05-03-2020)“…Prothioconazole is a broad spectrum anti-fungal agent of triazolinthione family; it has been widely used in crop protection especially in cereals. To date,…”
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5
An Efficient and Telescopic Process for Valsartan, an Angiotensin II Receptor Blocker
Published in Organic process research & development (20-04-2012)“…An efficient, telescopic, and scalable process for an antihypertensive drug substance, valsartan with an overall yield of 58%, and ∼99.9% purity is described…”
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6
Concise and Alternative Synthesis of Zafirlukast, an Anti-Asthma Drug
Published in Synthetic communications (01-01-2013)“…Concise and alternative synthesis of zafirlukast (1) is described. The synthesis features fewer steps, convergent synthesis, and novel intermediates…”
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7
Process Improvements of Prasugrel Hydrochloride: An Adenosine Diphosphate Receptor Antagonist
Published in Organic process research & development (17-02-2012)“…An improved process for the synthesis of prasugrel hydrochloride with an overall yield of 58%, 99.9% purity, and meeting all other quality requirements is…”
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8
An Improved Process for Pioglitazone and Its Pharmaceutically Acceptable Salt
Published in Organic process research & development (20-11-2009)“…An improved process for pioglitazone (1) is described. The process features high-yielding transformations employing inexpensive reagents and recoverable…”
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9
Improved Process for Ranolazine: An Antianginal Agent
Published in Organic process research & development (18-05-2012)“…An improved process has been developed for the active pharmaceutical ingredient, ranolazine with 99.9% purity and 47% overall yield (including three chemical…”
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10
An Efficient Synthesis of 1‑(2-Methoxyphenoxy)-2,3-epoxypropane: Key Intermediate of β‑Adrenoblockers
Published in Organic process research & development (19-10-2012)“…An efficient process for the preparation of 1-(2-methoxyphenoxy)-2,3-epoxypropane, a key intermediate for the synthesis of ranolazine is described…”
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11
New and Efficient Synthetic Approaches for the Regioisomeric and Iminium Impurities of Clopidogrel Bisulfate
Published in Organic process research & development (21-09-2012)“…New and concise synthetic routes have been devised for the regioisomeric and iminium impurities of clopidogrel bisulfate. The synthesis features utilization of…”
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12
An Improved and Scalable Process for Zafirlukast: An Asthma Drug
Published in Organic process research & development (16-01-2009)“…An improved and scalable process for the large-scale production of zafirlukast (Accolate), an important drug for asthma, is discussed along with impurity and…”
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13
Identification, characterization and synthesis of impurities of zafirlukast
Published in Journal of pharmaceutical and biomedical analysis (01-05-2009)“…Zafirlukast is a drug in the treatment of pulmonary disorders such as asthma. During the process development of zafirlukast, five unknown impurities were…”
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14
Alternative Synthesis of Tadalafil: PDE5 Inhibitor
Published in Synthetic communications (03-11-2008)“…Two-step alternative synthesis of tadalafil (1) is described. The synthesis features Pictet-Spengeler type reaction and DCC…”
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