Zobrazeno 1 - 10 of 13 pro vyhledávání: '"Ranga Prasad Dodda"'
1
Synthesis of Highly Substituted Imidazo[1,5-a]quinoxalines Through a Multicomponent Reaction Followed by Deprotection-Cyclization
Autor: Akanksha Upadhyay, Ranga Prasad Dodda, Ram K. Modukuri, Gopala Reddy Palnati, Koneni V. Sashidhara, Ruchir Kant
Publikováno v: Advanced Synthesis & Catalysis. 358:2612-2618
An operationally simple and efficient, one-pot, two-step methodology has been developed for the assembly of medicinally important imidazo[1,5-a]quinoxalines. The protocol involves the multicomponent reaction of aryl aldehydes, ortho-N-Boc-phenylenedi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::096cc9139b3c1f796d2c774ce9485413
https://doi.org/10.1002/adsc.201600285
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2
Synthesis and evaluation of novel triazolyl quinoline derivatives as potential antileishmanial agents
Autor: Karthik Ramalingam, Akanksha Upadhyay, Koneni V. Sashidhara, Neena Goyal, Sampa Gupta, Pragati Kushwaha, Ranga Prasad Dodda, Ruchir Kant
Publikováno v: European journal of medicinal chemistry. 154
The high potential of quinoline containing natural products and their derivatives in medicinal chemistry led us to discover novel series of 25 compounds for the development of new antileishmanial agents. A series of triazolyl 2-methyl-4-phenylquinoli
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::388142f62799a20ec1f2bf16994febdd
https://pubmed.ncbi.nlm.nih.gov/29793211
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3
Benzofuran-Chalcone Hybrids as Potential Multifunctional Agents against Alzheimer’s Disease: Synthesis and in vivo Studies with TransgenicCaenorhabditis elegans
Autor: Ranga Prasad Dodda, Vikash Kumar, Rizwanul Haque, Koneni V. Sashidhara, Balasubramaniam Sridhar, Ram K. Modukuri, Pooja Jadiya, Aamir Nazir, Mohammad Imran Siddiqi, Manoj Kumar
Publikováno v: ChemMedChem. 9:2671-2684
In the search for effective multifunctional agents for the treatment of Alzheimer's disease (AD), a series of novel hybrids incorporating benzofuran and chalcone fragments were designed and synthesized. These hybrids were screened by using a transgen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::feab6e76ef0ea87743a643976739451a
https://doi.org/10.1002/cmdc.201402291
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4
Design and synthesis of novel indole-chalcone fibrates as lipid lowering agents
Autor: Koneni V. Sashidhara, Ranga Prasad Dodda, Gopala Reddy Palnati, Gitika Bhatia, Ravi Sonkar
Publikováno v: European Journal of Medicinal Chemistry. 81:499-509
A series of novel indole-chalcone fibrates were synthesized and their hypolipidemic activity was evaluated in triton WR-1339 induced hyperlipidemic rat model. Preliminary studies indicated that the hybrids 19, 24 and 29 exhibited potent in vitro anti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29a662a7e6726beb08f854d4d20a68b9
https://doi.org/10.1016/j.ejmech.2014.04.085
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5
ChemInform Abstract: Synthesis of Highly Substituted Imidazo[1,5-a]quinoxalines Through a Multicomponent Reaction Followed by Deprotection-Cyclization
Autor: Ram K. Modukuri, Akanksha Upadhyay, Koneni V. Sashidhara, Ruchir Kant, Ranga Prasad Dodda, Gopala Reddy Palnati
Publikováno v: ChemInform. 47
An operationally simple and efficient, one-pot, two-step methodology has been developed for the assembly of medicinally important imidazo[1,5-a]quinoxalines. The protocol involves the multicomponent reaction of aryl aldehydes, ortho-N-Boc-phenylenedi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::56678273a1aea3374ca27809aa5fa6f3
https://doi.org/10.1002/chin.201652322
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6
One-Pot Regioselective Synthesis of Imidazole and 2,3-Dihydroquinazolinone Derivatives - An Easy Access to ‘Nature-Like Molecules'; Part XIII in the Series: ‘Studies on Novel Synthetic Methodologies'
Autor: Koneni V. Sashidhara, Gopala Reddy Palnati, Priyanka Swami, Ranga Prasad Dodda, Srinivasa Rao Avula
Publikováno v: Synlett. 24:1795-1800
A mild and highly practical regioselective synthesis of imidazole and 2,3-dihydroquinazolinone derivatives from 5-alkyl-4-hydroxyisophthalaldehydes with suitable substrates in acetic acid is reported. Further exploration of the molecular diversity of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7a2546c8afd2ebe9573cada724ee4f5e
https://doi.org/10.1055/s-0033-1339466
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7
Studies on Novel Synthetic Methodologies, Part XII: An Efficient One-Pot Access to 6,6a-Dihydroisoindolo[2,1-a]quinazoline-5,11-diones and 5-Phenylisoindolo[2,1-a]quinazolin-11(6aH)-ones
Autor: Priyanka Swami, Ranga Prasad Dodda, Srinivasa Rao Avula, Gopala Reddy Palnati, Koneni V. Sashidhara
Publikováno v: Synlett. 24:105-113
A simple and efficient procedure for the construction of 6,6a-dihydroisoindolo[2,1-a]quinazoline-5,11-dione and 5-phenylisoindolo[2,1-a]quinazolin-11(6aH)-one derivatives in acetic acid under catalyst-free conditions is described. Attractive features
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a9d980740aed876ee3cfa7ea20d404ba
https://doi.org/10.1055/s-0032-1317761
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8
A new iodine catalyzed regioselective synthesis of xanthene synthons
Autor: Koneni V. Sashidhara, Bikash Kumar, Abdhesh Kumar, Ranga Prasad Dodda
Publikováno v: Tetrahedron Letters. 53:3281-3283
This Letter describes the iodine catalyzed one-pot regioselective synthesis of p- condensed xanthenes as our key point of transformation, which provides an efficient access to five skeletally diverse scaffolds in excellent yields.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3adbe1e67ad678ff59364c5d9d736832
https://doi.org/10.1016/j.tetlet.2012.04.061
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