Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jayaprakash Rao Yerrabelli"'
Autor:
Kutumbarao Mattela, Madhu Gutam, Santosh Kumar Konda, Naveen Reddy Vadiyala, Jayaprakash Rao Yerrabelli, Prasad Rao Chitneni
Publikováno v:
Asian Journal of Chemistry. 34:1821-1824
A novel series of chromenone-benzimidazole/bezoxazole-1,2,3-triazole hybrids have been designed and synthesized using 4-hydroxy-chromenone. The 4-hydroxychromenone was used to produce terminal alkynated chromenone, which in turn reacted with differen
Autor:
Sudhakar Mokenapelli, Prasad Rao Chitneni, Vamshi Krishna Irlapati, Someswar Rao Sagurthi, Jayaprakash Rao Yerrabelli, Madhu Gutam, Neelima Gorityala
Publikováno v:
Russian Journal of Bioorganic Chemistry. 46:845-855
A new series of 2,5-regioselective benzofuran-tetrazole hybrids (XIIIa–XIIIp) were synthesised from 2H-chromene-3-carbonitriles (IXa), (IXb) in multi steps approach under mild reaction conditions in good yields and evaluated their anti-proliferativ
Autor:
Jayaprakash Rao Yerrabelli, Partha Pratim Roy, Sudhakar Mokenapelli, Prasad Rao Chitneni, Neeladrisingha Das
Publikováno v:
Natural Product Research. 35:3738-3744
Simple and efficient method was established for the synthesis of a new family of 14α-O-(andrographolide-3-subsitutedisoxazole-5-carboxylate) derivatives (10a-j) from naturally occurring andrographolide (1) by selective esterification with propiolic
Autor:
Sudhakar Mokenapelli, Naveen Vadiyaala, Rama Krishna Kancha, Someswar Rao Sagurthi, Madhu Gutam, Prasad Rao Chitneni, Somesh Banerjee, Jayaprakash Rao Yerrabelli, Bharathi Reddy Kunduru, Partha Roy
Publikováno v:
Natural Product Research. 35:289-297
A series of novel 14α-O-(1,4-disubstituted-1,2,3-triazolyl) ester derivatives of andrographolide (5a-n) were synthesized from andrographolide (1). For this endeavour, selective esterification at C-14 hydroxyl group of andrographolide (1) with propio
Autor:
Sudhakar, Mokenapelli, Jayaprakash Rao, Yerrabelli, Neeladrisingha, Das, Partha, Roy, Prasad Rao, Chitneni
Publikováno v:
Natural product research. 35(21)
Simple and efficient method was established for the synthesis of a new family of 14α
Autor:
Madhu Gutam, Prasad Rao Chitneni, Sudhakar Mokenapelli, Somesh Banerjee, Jayaprakash Rao Yerrabelli, Partha Pratim Roy
A series of new flavanone-triazole hybrids (7a���m) were synthesized from flavanone oximes (6a���c) via multistep synthetic strategy, involving Cu (I) catalyzed azide, alkyne 1,3-dipolar cycloaddition by Click reaction. All the synthesize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6703b4abb28ccc7f0ca871aa8719d9
Autor:
Jayaprakash Rao Yerrabelli, Prasad Rao Chitneni, Mohan Babu Bommagani, Sathish Kumar Boda, Sudhakar Mokenapelli
A new series of cinnoline-1,2,3-triazole derivatives were designed and synthesized by adopting Cu(1) catalyzed regeoselective1,3-dipolar cycloaddition reaction of terminal alkyne and azide. The in vitro antibacterial activity of all these compounds r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::777fe52764423d9e6f9e749a74158fb0
Autor:
Sudhakar, Mokenapelli, Madhu, Gutam, Naveen, Vadiyaala, Jayaprakash Rao, Yerrabelli, Somesh, Banerjee, Partha, Roy, Rama Krishna, Kancha, Bharathi Reddy, Kunduru, Someswar Rao, Sagurthi, Prasad Rao, Chitneni
Publikováno v:
Natural product research. 35(2)
A series of novel 14α