Výsledky vyhledávání - "Raghavender Medisetti"

Akademický článek

Mycobacterium tuberculosis Zinc Metalloprotease-1 assists mycobacterial dissemination in Zebrafish

Autor: Mani Harika Vemula, Raghavender medisetti, Rakesh Ganji, Kiran Jakkala, Swetha Sankati, Kiranam Chatti, Sharmistha Banerjee

Publikováno v: Frontiers in Microbiology, Vol 7 (2016)

Zinc metalloprotease-1 (Zmp1) from Mycobacterium tuberculosis (M.tb), the tuberculosis (TB) causing bacillus, is a virulence factor involved in inflammasome inactivation and phagosome maturation arrest. We earlier reported that Zmp1 was secreted unde

Externí odkaz: https://doaj.org/article/ad9512a8556a40b3a73f459e07d5d8da

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Copper-Catalyzed Domino Reaction Involving Nitro as an Unexpected Leaving Group: Construction of Dibenzo-Fused Azepinone Ring

Autor: Rajnikanth Sunke, Kishore V. L. Parsa, Pushkar Kulkarni, Ravikumar Kapavarapu, Raghavender Medisetti, Suresh Babu Nallapati, E. V. Venkat Shivaji Ramarao, Manojit Pal, Ramudu Bankala

Publikováno v: Advanced Synthesis & Catalysis. 358:3201-3205

A copper-catalyzed new domino reaction allowed the facile and direct construction of the dibenzo-fused azepinone ring leading to an array of novel small molecules. The co-catalyst, ligand or additive free one-pot method afforded a unique class of fun

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e5b252a48019e422b37cfeca7a6e385a
https://doi.org/10.1002/adsc.201600748

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Pd-catalyzed isocyanide insertion/nucleophilic attack by indole C-3/desulfonylation in the same pot: a direct access to indoloquinolines of pharmacological interest

Autor: Sunder Kumar Kolli, Suresh Babu Nallapati, Bagineni Prasad, Pushkar Kulkarni, Swapna Yellanki, Manojit Pal, Khagga Mukkanti, Shivashankar Sripelly, Raghavender Medisetti, Atul Kumar Sharma

Publikováno v: RSC Advances. 5:62966-62970

A new, simple and straightforward cascade reaction involving the Pd-catalyzed isocyanide insertion followed by a nucleophilic attack by the indole C-3 has been developed. The methodology afforded a diverse and unique class of indolo[2,3-b]quinolin-11

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::aa479f3c71a5b86303a5006d878a749a
https://doi.org/10.1039/c5ra13535d

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A Pd(ii)-catalyzed C–H activation approach to densely functionalized N-heteroaromatics related to neocryptolepine and their evaluation as potential inducers of apoptosis

Autor: Manojit Pal, Mohd Ashraf Ashfaq, Rajnikanth Sunke, Vimal Kumar, Pushkar Kulkarni, Raghavender Medisetti, Swapna Yellanki, E. V. Venkat Shivaji Ramarao, Nasreen Z. Ehtesham

Publikováno v: RSC Advances. 5:44722-44727

11-Carboxymethyl substituted 6H-indolo[2,3-b]quinolines, which are potential inducers of apoptosis, were obtained by one-pot Pd(II)-catalyzed intramolecular oxidative C3–H alkenylation of the indole ring of (E)-alkyl-3-(2-(1H-indol-2-ylamino)phenyl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b7e46c933271167dbcb171e3a530e87d
https://doi.org/10.1039/c5ra06764b

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Ligand-free Pd-catalyzed C–N cross-coupling/cyclization strategy: An unprecedented access to 1-thienyl pyrroloquinoxalines for the new approach towards apoptosis

Autor: Sunder Kumar Kolli, Girdhar Singh Deora, Raghavender Medisetti, Ali Nakhi, Sivakumar Archana, Pushkar Kulkarni, Maneesha Saridena, Swapna Yellanki, R. Ramesh Raju, Manojit Pal

Publikováno v: European Journal of Medicinal Chemistry. 86:270-278

The link between PDE4 and apoptosis prompted us to design and synthesize for the first time a series of novel 1-thienyl pyrroloquinoxalines as potential PDE4 inhibitors/apoptotic agents. A ligand-free Pd-catalyzed C-N cross-coupling/cyclization strat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01b0cd29ef4c387f2e323e9a5d14e670
https://doi.org/10.1016/j.ejmech.2014.08.057

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