Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Rajnikanth Sunke"'
Publikováno v:
Organic & Biomolecular Chemistry. 20:9148-9160
Indolyl substituted iodo-sulfonamides deliver 2-aryl(sulfonamido)indoles in the presence of Pd(OAc)2/Ph3P/Et3N; the same reactants, using Pd(OAc)2/Ph3P/K2CO3, afford indole-fused sultams.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3e98b43618506a3db9e35378f89fccd
https://doi.org/10.1039/d2ob01610a
https://doi.org/10.1039/d2ob01610a
Publikováno v:
Organicbiomolecular chemistry. 20(46)
Palladium-catalysed and base-dependent intra-molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::19fc700857574a507639a1e5bb52937f
https://pubmed.ncbi.nlm.nih.gov/36346226
https://pubmed.ncbi.nlm.nih.gov/36346226
Autor:
Kishore V. L. Parsa, Jayesh Mudgal, E.V.V. Shivaji Ramarao, Jetta Sandeep Kumar, Ramudu Bankala, Hari Maduri Doss, Mahaboobkhan Rasool, Manojit Pal, Rajnikanth Sunke, Pushkar Kulkarni, B. Thirupataiah, Ravikumar Kapavarapu, Gautham G. Shenoy, Raghavender Medishetti, Jessy Elizabeth Mathew
Publikováno v:
European Journal of Medicinal Chemistry. 174:198-215
A new class of PDE4 inhibitors were designed and synthesized via the InCl3 mediated heteroarylation of indoles and their further derivatization through the Pd(II)-catalyzed C H activation strategy. This effort allowed us to discover a series of 2-(1H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5aec68d5d4d21d2e7d1057a76f345800
https://doi.org/10.1016/j.ejmech.2019.04.020
https://doi.org/10.1016/j.ejmech.2019.04.020
Publikováno v:
The Journal of organic chemistry. 85(2)
A simple but efficient one-pot or sequential copper-catalyzed protocol using 2-bromoaldehydes and active methylene group containing substrates that affords multifunctional naphthalenes, phenanthrenes, quinolines, and benzo[b]carbazoles via Knoevenage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::758249b106d1ca600ab5d9c32273f095
https://pubmed.ncbi.nlm.nih.gov/31823603
https://pubmed.ncbi.nlm.nih.gov/31823603
Publikováno v:
Organic & Biomolecular Chemistry. 15:4042-4057
As a privileged class of heterocyclic compounds N-heteroarenes have found enormous applications in many areas including medicinal/pharmaceutical chemistry and drug discovery. Consequently, a wide variety of methods have been reported for their synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5715c85320bc341fa3a5664c5b4aedcc
https://doi.org/10.1039/c7ob00468k
https://doi.org/10.1039/c7ob00468k
Autor:
Rajnikanth, Sunke, Ramudu, Bankala, B, Thirupataiah, E V V Shivaji, Ramarao, Jetta Sandeep, Kumar, Hari Maduri, Doss, Raghavender, Medishetti, Pushkar, Kulkarni, Ravi Kumar, Kapavarapu, Mahaboobkhan, Rasool, Jayesh, Mudgal, Jessy E, Mathew, Gautham G, Shenoy, Kishore V L, Parsa, Manojit, Pal
Publikováno v:
European journal of medicinal chemistry. 174
A new class of PDE4 inhibitors were designed and synthesized via the InCl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e66dd42db0e6dc87d42308d03e873ecd
https://pubmed.ncbi.nlm.nih.gov/31035240
https://pubmed.ncbi.nlm.nih.gov/31035240
Autor:
Manojit Pal, Bagineni Prasad, Y. Poornachandra, K. Mukkanti, B. Yogi Sreenivas, Rajnikanth Sunke, B. Sridhar, Suresh Babu Nallapati, C. Ganesh Kumar, S. Shivashankar
Publikováno v:
Advanced Synthesis & Catalysis. 358:3387-3393
The formation of an amide bond via incorporation of two isocyanide units during a palladium‐catalyzed construction of the indoloquinoline ring afforded N‐substituted 6H‐indolo[2,3‐b]quinoline‐11‐carboxamides as new cytotoxic agents. The s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14f58c3813bdfcd223c70ec90ce31ef9
https://doi.org/10.1002/adsc.201600599
https://doi.org/10.1002/adsc.201600599
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
https://doi.org/10.1002/adsc.201600748
Autor:
Kishore V. L. Parsa, Vimal Kumar, Rajnikanth Sunke, Ramudu Bankala, Manojit Pal, E. V. Venkat Shivaji Ramarao
Publikováno v:
RSC Advances. 5:70604-70608
Quinoxaline has been identified as a new directing group for the Pd (or Ru)-catalyzed ortho C–H alkenylation of aniline derivatives and subsequent hypervalent iodine promoted intramolecular ortho C–H cycloamination of the resulting N-arylquinoxal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4737af20871afa4df4423355e86d3af4
https://doi.org/10.1039/c5ra14671b
https://doi.org/10.1039/c5ra14671b
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
https://doi.org/10.1039/c5ra06764b