Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Toreshettahally. R Swaroop"'
Publikováno v:
European Journal of Medicinal Chemistry Reports, Vol 12, Iss , Pp 100225- (2024)
Inflammation is a body response against infection that activates other biological components that include various cytokines, chemokines and other biological compounds that trigger body response against pathological activities. The Arachidonic acid pa
Externí odkaz:
https://doaj.org/article/a7a1ea8af64b4826a1296cd3180268ea
Autor:
Mahadev SHIVARAJ, Rajaghatta N SURESH, Toreshettahally R SWAROOP, Manikyanahally N KUMARA, Kanchugarakoppal S RANGAPPA, Kempegowda MANTELINGU, Adaganahalli Boregowda MAMATHA DEVI, Madihalli Prasanna MANASA, Muddegowda UMASHANKARA
Publikováno v:
Electrochemistry, Vol 91, Iss 12, Pp 122001-122001 (2023)
An electrochemical synthesis of 3,5-bis(acyl)-1,2,4-thiadiazoles by the oxidative dimerization of α-oxothioamides with assistance of tetra-n-butylammonium iodide (TBAI) as electrolyte and mediator under constant current electrolysis (CCE) is reporte
Externí odkaz:
https://doaj.org/article/d6d38ea2c6bd4403b7660fd892bc95fe
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:
Dukanya Dukanya, Toreshettahally R. Swaroop, Shobith Rangappa, Kanchugarakoppal S. Rangappa, Basappa Basappa
Publikováno v:
SynOpen, Vol 03, Iss 03, Pp 71-76 (2019)
Abstract Base-induced cyclization of active methylene isocyanides with carbamimidothioates for the synthesis of N,1-aryl-4-tosyl/ethylcarboxy-1H-imidazol-5-amines is reported. The diversity of the reactions is exemplified by using various carbamimido
Externí odkaz:
https://doaj.org/article/4a8e862d6d714d168142f96ebe52e2ac
Autor:
Rajaghatta N. Suresh, Toreshettahally R. Swaroop, Darshini Gowda, Kempegowda Mantelingu, Kanchugarakoppal S. Rangappa
Publikováno v:
RSC Advances. 13:4910-4916
Synthesis of thiazoles and thioethers.
Autor:
Toreshettahally R Swaroop, Kereyagalahally H Narasimhamurthy, Yarabhally R Girish, Kanchugarakoppal S Rangappa
Publikováno v:
Letters in Drug Design & Discovery. 20
Abstract: Among N-containing heterocycles, pyridine occupies a prominent position due to its presence in nature. Many enzymes in living systems, which are involved in redox reactions, contain pyridine moiety. In addition, its importance in medicinal
Autor:
Kanchugarakoppal. S Rangappa, Toreshettahally. R Swaroop, Kereyagalahally. H. Narasimhamurthy, Muthipeedika Nibin Joy, Ayyiliath M Sajith, Sougata Santra, Grigory V Zyryanov
Publikováno v:
Letters in Organic Chemistry. 20
Abstract: Various catalytic and non-catalytic organic transformations are carried out in glycerol media with superior efficiency over commonly employed organic solvents. The success of glycerol as a green media is due to its exceptional H-bonding pro
Autor:
Toreshettahally R. Swaroop, Chalya M. Shivaprasad, Ramesh Preetham, Maralinganadoddi P. Sadashiva, Kanchugarakoppal S. Rangappa
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 197:891-898
Autor:
Krishna Ravi Singh, Chikkappaiahnayaka Santhosh, Toreshettahally R. Swaroop, Maralinganadoddi P. Sadashiva
Publikováno v:
Organic & Biomolecular Chemistry. 20:5771-5778
Regioselective synthesis of 2-(methylthio)-N-aryl/alkylthiazole-5-carboxamides and ethyl-5-(aryl/alkylcarbamoyl)thiazole-4-carboxylates was carried out via the base-induced cyclization of methyl-2-oxo-2-(amino)ethanedithioates with TosMIC and ethyl i
Publikováno v:
Recent Progress in Chemical Science Research Vol. 6 ISBN: 9788119054039
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd366befb162fa3ca43af29aacc53801
https://doi.org/10.9734/bpi/rpcsr/v6/4920a
https://doi.org/10.9734/bpi/rpcsr/v6/4920a