Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Subburethinam, Ramesh"'
Autor:
Sesuraj Babiola Annes, Karuppaiah Perumal, Kalaiselvan Anandhakumar, Bhaskaran Shankar, Subburethinam Ramesh
Publikováno v:
The Journal of Organic Chemistry. 88:6039-6057
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79c872ab6a1abe948d45edf9cfe12635
https://doi.org/10.1021/acs.joc.3c00382
https://doi.org/10.1021/acs.joc.3c00382
Autor:
Rajendhiran Saritha, Sesuraj Babiola Annes, Karuppaiah Perumal, Bhaskaran Shankar, Subburethinam Ramesh
Publikováno v:
The Journal of Organic Chemistry. 87:13856-13872
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b5f660af31d224eb399210c1b954e40
https://doi.org/10.1021/acs.joc.2c01557
https://doi.org/10.1021/acs.joc.2c01557
Autor:
Karuppaiah Perumal, Subburethinam Ramesh, Sesuraj Babiola Annes, Anbazhagan Veerappan, Rajendhiran Saritha
Publikováno v:
ChemistrySelect. 6:12440-12445
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afa0a8319bef3964ea21efe5b92f6e25
https://doi.org/10.1002/slct.202102903
https://doi.org/10.1002/slct.202102903
Autor:
Kuppusamy Chandru, Sesuraj Babiola Annes, Rajendhiran Saritha, Pavan Kumar Mandali, Subburethinam Ramesh
Publikováno v:
The Journal of Organic Chemistry. 86:16473-16484
We developed an iodine-mediated cascade strategy to synthesize amino pyrazole thioether derivatives (11) in the absence of metals as well as solvents. The present approach provides amino pyrazole thioethers in a highly selective manner without the fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a29f7d15561392af61d7333cb8d6fa9
https://doi.org/10.1021/acs.joc.1c01846
https://doi.org/10.1021/acs.joc.1c01846
Autor:
Aleena Pious, Ravi Kanth Kamlekar, Sureshan Muthusamy, Arunachalam Jothi, Vijayendran K.K. Praneeth, Subburethinam Ramesh, Anbazhagan Veerappan
Publikováno v:
Colloids and Surfaces A: Physicochemical and Engineering Aspects. 664:131129
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd20c0727a7dff8c0318570675a735c7
https://doi.org/10.1016/j.colsurfa.2023.131129
https://doi.org/10.1016/j.colsurfa.2023.131129
Publikováno v:
RSC Advances. 11:14079-14084
Highly regioselective organo photocatalysis of 4CzIPN (1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene) for the arylation of 2H-indazole is demonstrated. The present synthetic route provides a highly safe and easily accessible aniline precursor as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f209aa1d13c626b596032020857f9563
https://doi.org/10.1039/d1ra02372a
https://doi.org/10.1039/d1ra02372a
Autor:
Kolanchinathan Nivedha, Siva Bala Subramaniyan, Manokaran Yuvasri, Veerappan Anbazhagan, Sesuraj Babiola Annes, Subburethinam Ramesh
Publikováno v:
ChemistrySelect. 5:515-521
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d75cfc69d21b59da7722b2dcc8c656bb
https://doi.org/10.1002/slct.201904169
https://doi.org/10.1002/slct.201904169
Autor:
Saravanan Subramanian, Sesuraj Babiola Annes, Subburethinam Ramesh, Bhaskaran Shankar, Rajendhiran Saritha
Publikováno v:
Green Chemistry. 22:2388-2393
A highly regioselective, solvent-free and montmorillonite K10 clay-catalyzed domino process with an unprecedented ring-closing C–C bond-formation reaction is described for the synthesis of a new class of 1,3,4-trisubstituted and 1,4-disubstituted p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bdfef729063486dbd9803ab32726c98
https://doi.org/10.1039/d0gc00162g
https://doi.org/10.1039/d0gc00162g
Publikováno v:
Bioconjugate chemistry. 32(8)
The disposition of a drug in a biological system may be altered by complex biological fluids; especially, protein binding to drugs influences their activity. Herein, we demonstrated a convenient method involving the noncovalent formulation of butea m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::044f5c9f98f7eb2eff2900c8aa75d180
https://pubmed.ncbi.nlm.nih.gov/34161072
https://pubmed.ncbi.nlm.nih.gov/34161072
Publikováno v:
Asian Journal of Organic Chemistry. 8:1398-1404
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b53738709177e6d10456ba3a5f8df015
https://doi.org/10.1002/ajoc.201900305
https://doi.org/10.1002/ajoc.201900305