Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Vanaparthi Satheesh"'
Autor:
Richa Gupta, Vanaparthi Satheesh, Nagaraju Vodnala, Raghuram Gujjarappa, Chandi C. Malakar, Arup K. Kabi, Dhananjaya Kaldhi
Publikováno v:
ChemistrySelect. 5:10144-10148
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e75e1be5677b556b1109d054734aef89
https://doi.org/10.1002/slct.202002968
https://doi.org/10.1002/slct.202002968
Autor:
Raghuram Gujjarappa, Dhananjaya Kaldhi, Vanaparthi Satheesh, Saibabu Polina, Nagaraju Vodnala, Chandi C. Malakar, Arup K. Kabi
Publikováno v:
New Journal of Chemistry. 44:20940-20944
A facile organocatalytic approach has been devised towards the synthesis of amide derivatives using 1,3-dicarbonyls as easily available acyl-sources under peroxide-free reaction conditions. This transformation was accomplished by the cleavage of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9a5929f67a7c7e3862689fbb358d57a
https://doi.org/10.1039/d0nj04158k
https://doi.org/10.1039/d0nj04158k
Autor:
Sivaparwathi Golla, Sanjeeva Thunga, Hari Prasad Kokatla, Soumya Poshala, Vanaparthi Satheesh
Publikováno v:
ChemistrySelect. 4:10466-10470
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68b23d0a4cb70c63883f1a91b71222c6
https://doi.org/10.1002/slct.201902189
https://doi.org/10.1002/slct.201902189
Autor:
Mani Sengoden, Sundaravel Vivek Kumar, Hemant Kumar Srivastava, Vanaparthi Satheesh, Tharmalingam Punniyamurthy
Publikováno v:
Advanced Synthesis & Catalysis. 361:55-58
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b865bab37b997f0b13ad44a273b32e2
https://doi.org/10.1002/adsc.201801116
https://doi.org/10.1002/adsc.201801116
Publikováno v:
Advanced Synthesis & Catalysis. 360:3030-3037
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8f164aaec1ee9e4064fe852c6e7c7dd
https://doi.org/10.1002/adsc.201800511
https://doi.org/10.1002/adsc.201800511
Autor:
Murugan Vijay, Sundaravel Vivek Kumar, Vanaparthi Satheesh, Tharmalingam Punniyamurthy, Debashis Barik
Publikováno v:
Asian Journal of Organic Chemistry. 7:1583-1586
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ee4ec846b518cf2de58194ce7ba4936
https://doi.org/10.1002/ajoc.201800274
https://doi.org/10.1002/ajoc.201800274
Autor:
Sundaram Ellairaja, Vanaparthi Satheesh, Vairathevar Sivasamy Vasantha, Tharmalingam Punniyamurthy, Sundaravel Vivek Kumar
Publikováno v:
Organic Chemistry Frontiers. 5:2630-2635
Rh(III)-Catalyzed regioselective C–H functionalization of 2-aryl-2H-indazoles with alkynes is reported to furnish indazoloquinolines utilizing Cu(OAc)2·H2O as an oxidant, which facilitates the reductive elimination step. Kinetic isotope studies su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee45c1365983b068a3a89347365a639e
https://doi.org/10.1039/c8qo00557e
https://doi.org/10.1039/c8qo00557e
Autor:
Thunga, Sanjeeva, Poshala, Soumya, Anugu, Naveenkumar, Konakanchi, Ramaiah, Vanaparthi, Satheesh, Kokatla, Hari Prasad
Publikováno v:
In Tetrahedron Letters 1 August 2019 60(31):2046-2048
Publikováno v:
Organic Letters. 19:6554-6557
Copper(II)-catalyzed cross-coupling of anilines, methyl arenes, and TMSN3 in the presence of tert-butylhydroperoxide at moderate temperature produced 2-aryl benzimidazoles via a tandem C(sp3/sp2)–H functionalization and C–N bond formations. The s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8947e9eb924ebeef8952d7dd51a4649e
https://doi.org/10.1021/acs.orglett.7b03264
https://doi.org/10.1021/acs.orglett.7b03264
Autor:
Sundaravel Vivek Kumar, Tharmalingam Punniyamurthy, Vairathevar Sivasamy Vasantha, Vanaparthi Satheesh, Murugan Vijay, Sundaram Ellairaja, Periyasamy Ananthappan, Hemant Kumar Srivastava
Publikováno v:
Organic letters. 21(18)
Sustainable assembly of imidazolidines is accomplished via a sequential stereospecific ring opening and C-H amination using aziridines with secondary cyclic amines under visible light mediated indazoloquinoline photoredox catalysis at ambient conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28356fcd917b1c0e8a1f18e66fab33ba
https://pubmed.ncbi.nlm.nih.gov/31486658
https://pubmed.ncbi.nlm.nih.gov/31486658