Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Prabhu P. Mohapatra"'
Autor:
Mangal S. Yadav, Abhishek Gupta, Priyanka Bose, Anoop S. Singh, Prabhu P. Mohapatra, Vinod K. Tiwari
Publikováno v:
SynOpen, Vol 07, Iss 03, Pp 430-465 (2023)
Externí odkaz:
https://doaj.org/article/ae6094a81db34ca99b8d4851508b6a47
Publikováno v:
ARKIVOC, Vol 2008, Iss 9, Pp 62-68 (2008)
Externí odkaz:
https://doaj.org/article/18f4a6a4e03f434eb1f1a06ff637a1b2
Autor:
ALAN R. KATRITZKY, PRABHU P. MOHAPATRA, SHAILENDRA SINGH, NICOLE CLEMENS, KOSTYANTYN KIRICHENKO
Publikováno v:
Journal of the Serbian Chemical Society, Vol 70, Iss 3, Pp 319-327 (2005)
Reactions of isonitriles 11a-c with N-(a-aminoalkyl)benzotriazoles 10a-k afford N-(a-aminoimidoyl)benzotriazoles 12a-q which on hydrolysis by dilute hydrochloric acid gave a-amino amides 14a-j.
Externí odkaz:
https://doaj.org/article/0ce5334ae72148cb8109a496be9f5a3a
Autor:
Alan R. Katritzky, Shailendra Singh, Prabhu P. Mohapatra, Nicole Clemens, Kostyantyn Kirichenko
Publikováno v:
ARKIVOC, Vol 2005, Iss 9, Pp 63-79 (2005)
Externí odkaz:
https://doaj.org/article/d1fd7c8952d949b78a0e9aa82dc1cb4e
Publikováno v:
ARKIVOC, Vol 2004, Iss 3, Pp 22-28 (2003)
Externí odkaz:
https://doaj.org/article/3ddc1e718fd14c45a8895555e7a95196
Autor:
Nidhi Mishra, Vinod K. Tiwari, Prabhu P. Mohapatra, Sumit K. Singh, Virendra Prasad, Anand K. Agrahari
Publikováno v:
Current Organic Chemistry. 23:768-808
Recent advances in high-throughput, automated techniques combined with the identification of new therapeutic targets in genome sequencing and molecular biology have generated a need for a large collection of diverse heterocyclic scaffolds. This inspi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74d48cc184c0378b371454b8bd55cfde
https://doi.org/10.2174/1385272823666190405145805
https://doi.org/10.2174/1385272823666190405145805
Autor:
Prabhu P. Mohapatra, Michele M. Kim, Alexander Greer, Andrés M. Durantini, Keith A. Cengel, Michael E. Zatoulovski, Mommina Ashaque, Theresa M. Busch, Timothy C. Zhu
This chapter is intended to help make inroads to the role of Intralipid in photodynamic therapy (PDT). In addition to Intralipid's favorable property as a light scattering agent, we hypothesized that it will be unstable to photosensitized oxidation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09565b91c05f612d09eaff19b9786d24
https://doi.org/10.1039/9781839162114-00411
https://doi.org/10.1039/9781839162114-00411
Autor:
Michele M. Kim, Timothy C. Zhu, Prabhu P. Mohapatra, Theresa M. Busch, Alexander Greer, Arina Kligman, Callistus Chiemezie
Publikováno v:
Photochemistry and Photobiology. 93:1430-1438
Intralipid is a lipid emulsion used in photodynamic therapy (PDT) for its light scattering and tissue-simulating properties. The purpose of this study is to determine whether or not Intralipid undergoes photooxidation, we have carried out an Intralip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4e117f7bf8699fcc9306de8a9c2817a
https://doi.org/10.1111/php.12810
https://doi.org/10.1111/php.12810
Autor:
Marilene Silva Oliveira, Kitae Kwon, Hellen Paula Valerio, Fernanda M. Prado, Edyta M. Greer, Alexander Greer, Ashwini A. Ghogare, Prabhu P. Mohapatra, Ciro J. Debaz, Inna Abramova, Paolo Di Mascio
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
A nitrosamine photooxidation reaction is shown to generate a peroxy intermediate by experimental physical-organic methods. The irradiation of phenyl and methyl-substituted nitrosamines in the presence of isotopically labeled 18-oxygen revealed that a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8ae7ef5b1ae6c3af30bad1f58a6f346
https://doi.org/10.1021/acs.jpca.7b02414
https://doi.org/10.1021/acs.jpca.7b02414
Autor:
Minati Kuanar, Amitabh Jha, Rachael Weagle, Donald Corkum, Melissa O’Brien, Prabhu P. Mohapatra
Publikováno v:
Molecular Diversity. 21:455-462
Substituted isoindoloquinolinones were obtained from N-aryl-3-hydroxyisoindolinones and aryl alkynes under Lewis acid-catalyzed conditions in 30–99% yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c02a8b7ca92208c20db90155a5ca3053
https://doi.org/10.1007/s11030-016-9718-3
https://doi.org/10.1007/s11030-016-9718-3