Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Padi, Pratap Reddy"'
Publikováno v:
In Journal of Saudi Chemical Society November 2014 18(5):513-519
Autor:
Padi Pratap Reddy, Anil S. Bobade, Ashish Asrondkar, Rajendra Patil, Satyanarayana Bollikonda, Sanjeev R. Patil, Devanand B. Shinde, Jaiprakash N. Sangshetti
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 28:482-487
A series of 5-substitutedbenzylideneamino-2-butylbenzofuran-3-yl-4-methoxyphenyl methanones is synthesized and evaluated for antileishmanial and antioxidant activities. Compounds 4f (IC50 = 52.0 ± 0.09 µg/ml), 4h (IC50 = 56.0 ± 0.71 µg/ml) and 4l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6faba2f9c7a6bbc4379e9482f3e8fe2d
https://doi.org/10.1016/j.bmcl.2017.12.013
https://doi.org/10.1016/j.bmcl.2017.12.013
Autor:
Padi Pratap Reddy, G. Mahesh Reddy, Koilkonda Purandhar, Kagga Mukkanti, Murugulla Adharvana Chari
Publikováno v:
Letters in Organic Chemistry. 11:81-90
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c195938a61fb0aa018bedaf35dba9e0
https://doi.org/10.2174/1570178610999131231123427
https://doi.org/10.2174/1570178610999131231123427
Autor:
Padi Pratap Reddy, Bolugoddu Vijayabhaskar, Bollikonda Satyanarayana, Chandrashekar R. Elati, Saravanan Mohanarangam
Publikováno v:
Journal of the Chinese Chemical Society. 58:841-845
A novel and efficient synthesis of dronedarone hydrochloride starting from 2-n-butyl-5-nitrobenzofuran by employing mild and selective reaction conditions is described. The synthetic approach is operationally simple and suitable for industrial applic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cbb997f07eaa3ddbe0f9db645246a66
https://doi.org/10.1002/jccs.201190133
https://doi.org/10.1002/jccs.201190133
Autor:
Aalla Sampath, Gilla Goverdhan, Rakeshwar Bandichhor, Anumula Raghupathi Reddy, Padi Pratap Reddy, Khagga Mukkanti
Publikováno v:
Synthetic Communications. 42:639-649
A large scale synthesis of valdecoxib 1 is described. Our work features potential application of [3 + 2]-dipolar cycloaddition involving enamine and in situ–generated nitrile oxide derivatives.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eba49fa8e72d42b159f0170d017940f8
https://doi.org/10.1080/00397911.2010.528572
https://doi.org/10.1080/00397911.2010.528572
Publikováno v:
Organic Process Research & Development. 15:1392-1395
An improved and impurity-free synthetic method for large-scale synthesis of venlafaxine hydrochloride was developed using inexpensive reagents. The overall yield obtained from this newly developed process is 55% in a highly pure state with >99.9% pur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8053c29730a97b779372c7ebe97ebe76
https://doi.org/10.1021/op200221y
https://doi.org/10.1021/op200221y
Autor:
Rakeshwar Bandichhor, Dinesh S. Bhalerao, G. C. M. Kondaiah, Padi Pratap Reddy, Arnab Roy, Apurba Bhattacharya, Lakkala Amarnath Reddy, Gudimalla Nagaraju, Ravi Kumar Mylavarappu, Namrata Dwivedi
Publikováno v:
Synthetic Communications. 40:2983-2987
A novel approach for the synthesis of omeprazole, a potent antiulcer drug, is described. The synthetic procedure involved the formation of an ester of the 5-methoxy thiobenzimidazole followed by coupling of the ester with the Grignard reagent of 2-ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c97d9b74a9903228d72b10d8639f836a
https://doi.org/10.1080/00397910903341171
https://doi.org/10.1080/00397910903341171
Publikováno v:
Synthetic Communications. 40:1880-1886
Venlafaxine hydrochloride is a phenyl ethylamine derivative, used for the treatment of depression. During the process development of venlafaxine hydrochloride, six process-related potential impurities were detected in high-performance liquid chromato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e6efb0e81b8243e3b61c56c17c626ad
https://doi.org/10.1080/00397910903162767
https://doi.org/10.1080/00397910903162767
Autor:
G. Venkateswarlu, Gade Srinivas Reddy, Padi Pratap Reddy, Amirisetty Ravindranath Tagore, Karrothu Srihari Babu, Ramasamy Vijaya Anand
Publikováno v:
ARKIVOC, Vol 2010, Iss 2, Pp 292-302 (2010)
Olmesartan medoxomil 1 is the latest angiotensin receptor antagonist approved by the FDA for the treatment of hypertension. During the process development of olmesartan medoxomil, four related substances (impurities) were observed along with the fina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf48ed045c41d1e6791de7512e48a54
https://doi.org/10.3998/ark.5550190.0011.224
https://doi.org/10.3998/ark.5550190.0011.224
Publikováno v:
Letters in Organic Chemistry. 7:45-49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b05fb0cfdc21e26f76586bf329fcc63
https://doi.org/10.2174/157017810790533878
https://doi.org/10.2174/157017810790533878