Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Mukkanti Kagga"'
Autor:
Rao, VascuriJanardhana1,2 (AUTHOR), Mukkanti, Kagga2 (AUTHOR), Vekariya, N.A.1 (AUTHOR), Gupta, P.Badrinadh1 (AUTHOR), Islam, Aminul1 (AUTHOR) aminulislam@aurobindo.com
Publikováno v:
Synthetic Communications. Nov2012, Vol. 42 Issue 21, p3200-3210. 11p.
Autor:
Golla China Malakondaiah, Vivekananda Reddy Mothukuri, Aminul Islam, Satish Kumar Vujjini, Rakeshwar Bandichhor, Mukkanti Kagga
Publikováno v:
Synthetic Communications. 43:3294-3306
Efficient and cost-effective synthesis of Zolmitriptan 1 employing Japp–Klingemann reaction and a new robust purification strategy is described.
Autor:
Satish Kumar Vujjini, Mukkanti Kagga, Srinivas Arevelli, Satyanarayana Raju Tirumalaraju, Sreenatha Charyulu Kandala, Rakeshwar Bandichhor, Praveen Cherukupally, Ganesh Varanasi
Publikováno v:
Organic Process Research & Development. 17:303-306
An improved, practical, and scalable process for the manufacture of antineoplastic drug, 5-azacytidine (1), is described. A thorough understanding of the reaction parameters and stability of the reaction intermediates led us to the development of a r
Autor:
Raghupathi Reddy Anumala, Rakeshwar Bandichhor, Mukkanti Kagga, Goverdhan Gilla, Lokeswara Rao Madivada
Publikováno v:
Organic Process Research & Development. 16:1660-1664
An efficient process for the preparation of 1-(2-methoxyphenoxy)-2,3-epoxypropane, a key intermediate for the synthesis of ranolazine is described.
Publikováno v:
African Journal of Pharmacy and Pharmacology. 5:207-213
A novel, simple and economic reverse phase high performance liquid chromatography (RP-HPLC) method has been developed for the estimation of rimonabant hydrochloride in bulk and tablet dosage forms with greater precision and accuracy. Separation was a
Autor:
Praveen Cherukupally, Satish Kumar Vujjini, V. N. K. V. Prasada Raju Vetukuri, Krishna Rao Badarla, Rakeshwar Bandichhor, Mukkanti Kagga, V. R. Krishnam Raju Datla
Publikováno v:
Tetrahedron Letters. 55:3885-3887
Total synthesis of antidepressant drug, agomelatine is reported. Regio selective Friedel–Crafts acylation followed by Willgerodt–Kindler reactions is used as the key steps for the synthesis of agomelatine.
Autor:
Lokeswara Rao Madivada, Mukkanti Kagga, Rakeshwar Bandichhor, Kavitha Charagondla, Goverdhan Gilla, Apurba Bhattacharya, Raghupathi Reddy Anumala, Sampath Alla
Publikováno v:
Organic Process Research & Development. 13:1190-1194
An improved process for pioglitazone (1) is described. The process features high-yielding transformations employing inexpensive reagents and recoverable solvents.
Autor:
Apurba Bhattacharya, Goverdhan Gilla, Lokeswara Rao Madivada, Padi Pratap Reddy, Mukkanti Kagga, Raghupathi Reddy Anumula, V. V. N. K. Prasad Raju, Rakeshwar Bandichhor
Publikováno v:
Synthetic Communications. 38:4265-4271
Two-step alternative synthesis of tadalafil (1) is described. The synthesis features Pictet–Spengeler type reaction and DCC (N,N′-dicyclohexylcarbodiimide)/HOBt (N-hydroxybenzotriazole)–mediated double amidation employing sarcosine ethyl ester
Autor:
Praveen Cherukupally, Krishna Rao Badarla, Satish Kumar Vujjini, Mukkanti Kagga, V. R. Krishnam Raju Datla, V. N. K. V. Prasada Raju Vetukuri, Rakeshwar Bandichhor
Publikováno v:
ChemInform. 46
Total synthesis of antidepressant drug, agomelatine is reported. Regio selective Friedel–Crafts acylation followed by Willgerodt–Kindler reactions is used as the key steps for the synthesis of agomelatine.
Autor:
Satish Kumar Vujjini, Krishna Rao Badarla, Sunitha Vyala, Mukkanti Kagga, Praveen Cherukupalli, Sreenatha Charyulu Kandala, Rakeshwar Bandichhor
A simple and efficient process for the large-scale preparation of agomelatine (1), an antidepressant drug is, described. Agomelatine was prepared in a linear manner starting from readily available, inexpensive 2-naphthol. Key steps in the synthesis a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::273ca667cff02ccbba6a8d2b755759d5