Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Nimesh C. Misra"'
Autor:
Aaramadaka Sunil Kumar Reddy, Siva Rama Kasibabu Velugula, Ramadas Chavakula, Paul Douglas Sanasi, Nimesh C. Misra, Anil Kumar Guduri, Pindi Santhosh Reddy
Publikováno v:
Journal of Heterocyclic Chemistry. 58:1581-1587
Autor:
Chandiran Takshinamoorthy, Paul Douglas Sanasi, Raghubabu Korupolu, Koilpillai Joseph Prabahar, Srinivas Garaga, Ambati V. Raghava Reddy, Nimesh C. Misra
Publikováno v:
Current Issues in Pharmacy and Medical Sciences, Vol 28, Iss 2, Pp 72-76 (2015)
This paper provides a description of an alternative, novel and commercially viable process which has been developed for the preparation of Azilsartan, a pro-drug of Azilsartan medoxomil, an angiotensin II receptor blocker. The present work also provi
Autor:
Nimesh C. Misra, Korupolu Raghu Babu, Ambati V. Raghava Reddy, Chandiran Takshinamoorthy, Paul Douglas Sanasi, Srinivas Garaga, Koilpillai Joseph Prabahar
Publikováno v:
Organic Process Research & Development. 19:514-519
A commercially viable process for the preparation of azilsartan kamedoxomil, an angiotensin II receptor blocker, has been developed. The present work describes the novel synthesis of azilsartan medoxomil from amidoxime methyl ester. The present work
Publikováno v:
Tetrahedron Letters. 50:366-369
An efficient one-pot, three-component synthesis of novel 2-substituted-5-aryl-1-oxo-3-thioxo-1,2,3,5,11,11a-hexahydro-6H-imidazo-[1,5-b]-β-carbolines employing 1-aryl-1,2,3,4-tetrahydro-β-carboline-3-carboxylates, primary amines (or amino acid este
Publikováno v:
Organic letters. 15(20)
The title reaction provides a direct entry to a range of biologically relevant annulated pyrroles via a domino process involving a regioselective one-carbon homologation of cyclic ketones as the key step.
Publikováno v:
ChemInform. 44
Regioselective ring opening of oxazolones of type (IV) [inter alia precursors of aminocarboxylic acids (II)] by diverse nucleophiles followed by Cu-catalyzed ring closure of resulting enamides provides an efficient approach to various 2-phenyl-4,5-su
Publikováno v:
The Journal of organic chemistry. 77(23)
An efficient two-step synthesis of 2-phenyl-4,5-substituted oxazoles involving intramolecular copper-catalyzed cyclization of highly functionalized novel β-(methylthio)enamides as the key step has been reported. These enamides are obtained by nucleo
Autor:
Wei-Ting Sun, Jye-Shane Yang, Ying-Chih Lin, Cheng-Hua Yang, Ch. Prabhakar, Shou-Ling Huang, Nimesh C. Misra, Wei Shyang Tan
Publikováno v:
Organic letters. 13(20)
A pentiptycene-derived p-phenylenediamine mimics a molecular double-rotor system that displays redox-dependent rotation rates for the amino rotors about the pentiptycene-amine C–N bond. The rotation is accelerated in the radical cation state but st
Autor:
Nimesh C. Misra, Hiriyakkanavar Ila
Publikováno v:
ChemInform. 41
4-Bis(methylthio)methylene-2-phenyloxazol-5-one has been shown to be a versatile template for the synthesis of various 2-phenyl-3,4-substituted oxazoles via nucleophilic ring-opening of oxazolone with various oxygen, nitrogen, and carbon nucleophiles
Autor:
Nimesh C. Misra, Hiriyakkanavar Ila
Publikováno v:
The Journal of organic chemistry. 75(15)
4-Bis(methylthio)methylene-2-phenyloxazol-5-one has been shown to be a versatile template for the synthesis of various 2-phenyl-3,4-substituted oxazoles via nucleophilic ring-opening of oxazolone with various oxygen, nitrogen, and carbon nucleophiles