Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Kempegowda, Mantelingu"'
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:
Gullahalli S. Jagadeesha, Kempegowda Mantelingu, Naraganahalli R. Thimmegowda, Kanchugarakoppal S. Rangappa
Publikováno v:
SynOpen, Vol 06, Iss 02, Pp 132-140 (2022)
Externí odkaz:
https://doaj.org/article/6ca0b9dbe0ff4316878acd51b2f8f758
Autor:
Sadashivamurthy Shamanth, Kempegowda Mantelingu, Haruvegowda Kiran Kumar, Hemmige S. Yathirajan, Sabine Foro, Christopher Glidewell
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 76, Iss 1, Pp 18-24 (2020)
Three title compounds, namely, 2-(4-chlorobenzyl)-5-[(1H-indol-3-yl)methyl]-6-phenylimidazo[2,1-b][1,3,4]thiadiazole, C26H19ClN4S, (I), 2-(4-chlorobenzyl)-6-(4-fluorophenyl)-5-[(1H-indol-3-yl)methyl]imidazo[2,1-b][1,3,4]thiadiazole, C26H18ClFN4S, (II
Externí odkaz:
https://doaj.org/article/cc7dffc27bd94b67befe774be16d7063
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.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::396dadf017a6ab023a617b9a010ecbf8
https://doi.org/10.1039/d2ra08118k
https://doi.org/10.1039/d2ra08118k
Autor:
Kanchugarakoppal S. Rangappa, Naraganahalli R. Thimmegowda, Gullahalli S. Jagadeesha, Kempegowda Mantelingu
Publikováno v:
SynOpen. :132-140
An efficient, environmentally benign, chemoselective, microwave-assisted N-formylation protocol of aromatic, aliphatic, alicyclic, benzylic amines, inactivated aromatic amines and sterically demanding heterocyclic amines using 2-formyl-1,3-dimethyl-1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62ed3637e34dd25de6e6d0db69753a44
https://doi.org/10.1055/s-0041-1737605
https://doi.org/10.1055/s-0041-1737605
Publikováno v:
Journal of Analytical Chemistry. 77:301-307
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c2ba1094192d3ced5428730b8742d42
https://doi.org/10.1134/s1061934822030091
https://doi.org/10.1134/s1061934822030091
Autor:
Ujjayinee Ray, Vindya K. Gopinatha, Shivangi Sharma, Laijau Goyary, Bibha Choudhary, Kempegowda Mantelingu, Kanchugarakoppal S. Rangappa, Sathees C. Raghavan
Publikováno v:
The FEBS journalReferences.
Mercaptopyrimidine derivatives are heterocyclic compounds with potent biological activities including antiproliferative, antibacterial, and anti-inflammatory properties. The present study describes the synthesis and characterization of several mercap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edb7b6d00577a026908e4326f50e8cd9
https://pubmed.ncbi.nlm.nih.gov/36048168
https://pubmed.ncbi.nlm.nih.gov/36048168
Autor:
null Ujjayinee Ray, null Vindya K. Gopinatha, null Shivangi Sharma, null Laijau Goyary, null Bibha Choudhary, null Kempegowda Mantelingu, null Kanchugarakoppal S. Rangappa, null Sathees C. Raghavan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5348311233d0d890cce03602c295e4c
https://doi.org/10.1111/febs.16615/v2/response1
https://doi.org/10.1111/febs.16615/v2/response1
Autor:
Kanchugarkoppal S. Rangappa, Ayyiliath M. Sajith, Srinivas Cheruku, Yatheesh Narayana, Sandhya C. Nagarakere, Kunigal S. Sagar, Kempegowda Mantelingu, Poornima Shetty, Kumara N Manikyanally
Publikováno v:
The Journal of Organic Chemistry. 86:5530-5537
Carbonylation of (hetero)aryl iodides/bromides with highly deactivated 2-aminopyridines using Pd-Co(CO)4 bimetallic catalysis is accomplished. The use of Co2(CO)8 as a solid CO(g) source enhanced reaction rates observed when compared to CO(g), and ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad177f19d70e5de5680cb4bd082d6421
https://doi.org/10.1021/acs.joc.0c02999
https://doi.org/10.1021/acs.joc.0c02999
Autor:
Sridhar B. Thimmaiah, Kanchugarakoppal S. Rangappa, H.E. Dinesh, Kempegowda Mantelingu, Yatheesh Narayana, Nagarakere C. Sandhya
Publikováno v:
Carbene
Arduengo et al., isolated the first ‘bottleable’ carbene, the first N-heterocyclic carbene (NHC) 1,3-di(adamantyl)imidazol-2-ylidene resulted to an explosion of experimental and theoretical studies of novel NHCs being synthesized and analyzed hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e69ff7898c7e1bddb29e940a21dbfdd
https://doi.org/10.5772/intechopen.100642
https://doi.org/10.5772/intechopen.100642