Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kuppalli R. Kiran"'
Autor:
Narasimhamurthy Rajeev, Toreshettahally R. Swaroop, Ahmad I. Alrawashdeh, Shofiur Rahman, Abdullah Alodhayb, Seegehalli M. Anil, Kuppalli R. Kiran, Chandra, Paris E. Georghiou, Kanchugarakoppal S. Rangappa, Maralinganadoddi P. Sadashiva
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 159-167 (2020)
An unexpected formation of carbamothioates by a sodium hydride-mediated reaction of arylmethyl isocyanides with xanthate esters in DMF is reported. The products thus obtained were compared with the carbamothioates obtained by the sodium hydride-media
Externí odkaz:
https://doaj.org/article/fe9fad0d80ca490a8c13d09780718e46
Autor:
Jeegundipattana B. Shruthi, Kuppalli R. Kiran, Shivakumar Divyashree, Marikunte Y. Sreenivasa, Maralinganadoddi P. Sadashiva
Publikováno v:
Journal of Heterocyclic Chemistry. 60:566-575
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f96dab74a450d54e55e9ae738daf0b23
https://doi.org/10.1002/jhet.4608
https://doi.org/10.1002/jhet.4608
Autor:
Kuppalli R. Kiran, Toreshettahally R. Swaroop, Ramesh Preetham, Paris E. Georghiou, Kanchugarakoppal S. Rangappa, Maralinganadoddi P. Sadashiva
Publikováno v:
ChemistrySelect. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::509f2e0ac907a1861f220b35529f01d8
https://doi.org/10.1002/slct.202203618
https://doi.org/10.1002/slct.202203618
Autor:
Maralinganadoddi P. Sadashiva, Jeegundipattana B. Shruthi, Kuppalli R. Kiran, Kodagahally T. Gunashree, S. Divyashree, Marikunte Y. Sreenivasa, Kanchugarakoppal S. Rangappa
Publikováno v:
Letters in Drug Design & Discovery. 20
aims: N-(1-benzylpiperidin-4-yl)quinoxalin-2-amines were synthesized and evaluated for antisalmonella activity against S. paratyphi. background: The most common cause of foodborne illness is bacterial or viral contamination. Although there are severa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ec7a74d3b75460d34879745bd4de2fb
https://doi.org/10.2174/1570180820666221226152736
https://doi.org/10.2174/1570180820666221226152736
Autor:
Ramesh Preetham, Malahalli S. Vijaya Kumar, Toreshettahally R. Swaroop, S. Divyashree, Kuppalli R. Kiran, Marikunte Y. Sreenivasa, Maralinganadoddi P. Sadashiva, Kanchugarakoppal S. Rangappa
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::891a871e0cbdfddf7e73b025f4293584
https://doi.org/10.1002/slct.202203079
https://doi.org/10.1002/slct.202203079
Autor:
Chikkappaiahnayaka Santhosh, Toreshettahally R. Swaroop, Kuppalli R Kiran, Maralinganadoddi P. Sadashiva, Kanchugarakoppal S. Rangappa
Publikováno v:
ChemistrySelect. 6:7262-7265
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0552614344ae69eec9d017301f4f8110
https://doi.org/10.1002/slct.202102071
https://doi.org/10.1002/slct.202102071
Autor:
Maralinganadoddi P. Sadashiva, Kuppalli R Kiran, Toreshettahally R. Swaroop, Seegehalli M Anil, Narasimhamurthy Rajeev, Kanchugarakoppal S. Rangappa
Publikováno v:
Synthesis. 52:1444-1450
Cyclization of tosylmethyl isocyanide with α-oxodithioesters in the presence of KOH is reported for the synthesis of 4-methylthio-5-acylthiazoles. Similarly, ethyl isocyanoacetate underwent cyclization with α-oxodithioesters to form 4-ethoxycarbony
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b01ec83bd5eb1cb4c1d80da1eb9551d
https://doi.org/10.1055/s-0039-1690821
https://doi.org/10.1055/s-0039-1690821
Autor:
Kanchugarakoppal S. Rangappa, Paris E. Georghiou, Chandra, Shofiur Rahman, Kuppalli R Kiran, Seegehalli M Anil, Ahmad I. Alrawashdeh, Toreshettahally R. Swaroop, Maralinganadoddi P. Sadashiva, Abdullah Alodhayb, Narasimhamurthy Rajeev
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 159-167 (2020)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
An unexpected formation of carbamothioates by a sodium hydride-mediated reaction of arylmethyl isocyanides with xanthate esters in DMF is reported. The products thus obtained were compared with the carbamothioates obtained by the sodium hydride-media
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11d13da2aa3c862c4143a45a442fda6a
https://doaj.org/article/fe9fad0d80ca490a8c13d09780718e46
https://doaj.org/article/fe9fad0d80ca490a8c13d09780718e46
Autor:
Kanchugarakoppal S. Rangappa, Toreshettahally R. Swaroop, Kuppalli R Kiran, Seegehally M Anil, Maralinganadoddi P. Sadashiva, Jeegundipattana B Shruthi, Kodipura P. Sukrutha
Publikováno v:
Synthesis. 51:4205-4214
o-Phenylenediammines and o-aminophenols were reacted with α-oxodithioesters in a highly regioselective fashion to give 2-methylthio-3-aryl/heteroarylquinoxalines and 2-acylbenzoxazoles in 55–94% and 45–86%, respectively, in the presence of p-tol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11a1865c830bcde32c7858b10ae4606a
https://doi.org/10.1055/s-0039-1690616
https://doi.org/10.1055/s-0039-1690616
Autor:
Rangappa Shobith, Ningegowda Mallesha, Kuppalli R Kiran, Toreshettahally R. Swaroop, Maralinganadoddi P. Sadashiva, Seegehalli M Anil, Narasimhamurthy Rajeev
Publikováno v:
International Journal of Peptide Research and Therapeutics. 26:151-158
In an attempt to develop synergetic, potential and selective anti-oxidant agents, a series of novel piperazine bridged pseudo-peptidic urea/thiourea derivatives (5a-x) are designed by molecular docking study, synthesized and evaluated for their in-vi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dad64e3269f922bb113923faa7b69482
https://doi.org/10.1007/s10989-019-09824-4
https://doi.org/10.1007/s10989-019-09824-4