Zobrazeno 1 - 10
of 268
pro vyhledávání: '"Mukund K. Gurjar"'
Autor:
Anil U. Chopade, Manojkumar U. Chopade, Bhanu M. Chanda, Dilip D. Sawaikar, Kiran B. Sonawane, Mukund K. Gurjar
Publikováno v:
Arabian Journal of Chemistry, Vol 9, Iss S2, Pp S1597-S1602 (2016)
A synthesis of (±)-thia-calanolide A 3 has been successfully accomplished starting from 3,5-dimethoxythiophenol 4, in six steps in an overall yield of 4.5%. The key reaction involved Friedel–Crafts tigloylation of 5,7-dihydroxy-4-n-propyl thiocoum
Externí odkaz:
https://doaj.org/article/838ec68b32654374b10ed01f7e56019b
Publikováno v:
ARKIVOC, Vol 2005, Iss 3, Pp 237-257 (2005)
Externí odkaz:
https://doaj.org/article/e9eaba881fb2452cb2f642c78ba97f17
Autor:
Sudhir P. Chaskar, Ramchandra Honparkhe, Jagdish Chavan, Amit Dhumal, Narendra K. Tripathy, Chinmoy Pramanik, Ashok Chaudhari, Rakesh G. Thorat, Mukund K. Gurjar
Publikováno v:
Journal of Heterocyclic Chemistry.
Autor:
Ashok Chaudhari, Chinmoy Pramanik, Pradeep Patil, Hanmant Vedpathak, Mahesh Bandishti, Narendra K. Tripathy, Mukund K. Gurjar
Publikováno v:
Journal of Heterocyclic Chemistry. 59:1054-1063
Autor:
D. D. Sawaikar, Mukund K. Gurjar, Manojkumar U. Chopade, Kiran B. Sonawane, Bhanu M. Chanda, Anil U. Chopade
Publikováno v:
Arabian Journal of Chemistry, Vol 9, Iss S2, Pp S1597-S1602 (2016)
Arabian Journal of Chemistry
Arabian Journal of Chemistry
A synthesis of (±)-thia-calanolide A 3 has been successfully accomplished starting from 3,5-dimethoxythiophenol 4, in six steps in an overall yield of 4.5%. The key reaction involved Friedel–Crafts tigloylation of 5,7-dihydroxy-4-n-propyl thiocoum
Autor:
Rangarao Kolla, Mukund G. Kulkarni, Narendra Kumar Tripathy, Chinmoy Pramanik, Srinivasarao Sompalli, Kiran Bapat, Ashok Chaudhari, Mukund K. Gurjar
Publikováno v:
Organic Process Research & Development. 18:495-500
Commercial manufacturing of benzphetamine hydrochloride along with its impurity profiling is disclosed. Deoxygenation of pseudoephedrine is reported with ∼100% retention by shielding the amine group as its tert-butyl carbamate, which is very straig
Autor:
Mukund K. Gurjar, Narendra Kumar Tripathy, Sandeep Kotharkar, Yogesh More, Tushar P. Khaladkar, Balaji Vasant Chaugule, Kaliaperumal Neelakandan, Ashok Chaudhari, Ajit S. Borhade, Mukund G. Kulkarni, Chinmoy Pramanik, Pradip Patil, Dinkar Gotrane
Publikováno v:
Organic Process Research & Development. 18:152-156
A commercially viable manufacturing process for propofol (1) is described. The process avoids acid–base neutralization events during isolation of intermediate, 2,6-di-isopropylbenzoic acid (3) and crude propofol, and thus simplifies the synthesis o
Publikováno v:
Organic Process Research & Development. 16:1591-1597
Darifenacin is a potent and competitive M3 selective receptor antagonist (M3SRA), and its hydrobromide salt (1) is the active ingredient of pharmaceutical formulations for oral treatment of urinary incontinence. The present work demonstrates an effic
Autor:
Swapnil Panditrao Sonawane, Ashok Chaudhari, Mukund K. Gurjar, Shivnath B. Shinde, Mangesh S. Deshpande, Siddheshwar W. Kshirsagar, Golak C. Maikap, Gulabrao D. Patil, Pankaj Shallkrao Patil
Publikováno v:
Organic Process Research & Development. 16:1422-1429
Multiple sources of anticipated degradation and process impurities of raltegravir potassium drug substance observed during the laboratory optimization and later during its bulk synthesis are described in this article. The impurities were monitored by
Publikováno v:
Current Organic Chemistry. 16:1159-1168