Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Santhakumar, Yeswanth Kumar"'
Autor:
Rathinam Sankar, Vasuki Gnanasambandam, Santhakumar Yeswanth Kumar, Jisha Mary Thomas, Thayalaraj Christopher Jeyakumar
Publikováno v:
Chemical Physics Impact, Vol 8, Iss , Pp 100530- (2024)
We have successfully synthesized our desired compound of (E)-3-benzylidene-9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one by reacting with 9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one and benzaldehyde. Further structure was characterized and confirme
Externí odkaz:
https://doaj.org/article/eb94081b8c0c48d69fa6132d1eaec55b
Publikováno v:
In Journal of Molecular Structure 15 October 2024 1314
Publikováno v:
Chemphyschem : a European journal of chemical physics and physical chemistry.
Quantum wave packet dynamics of the Li(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::62ccec8bc0f9ffa52c880cd996b195f2
https://pubmed.ncbi.nlm.nih.gov/36345664
https://pubmed.ncbi.nlm.nih.gov/36345664
Autor:
R. Padmanaban, Muthupandi Karthick, Chinnasamy Ramaraj Ramanathan, Kesa Venkatanna, Santhakumar Yeswanth Kumar
Publikováno v:
Organic & Biomolecular Chemistry. 17:4077-4086
A conformationally rigid chiral bicyclic skeleton tethered bipyridine–Zn(OTf)2 complex facilitated the enantioselective Friedel–Crafts alkylation of indoles with trans-β-nitroarylalkenes in an enantioselective manner at elevated temperature. Ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a26ca4a435745b6991f56cf6ee4ae2f5
https://doi.org/10.1039/c9ob00545e
https://doi.org/10.1039/c9ob00545e
Autor:
R. Padmanaban, Antony Stalin, Subban Kamalraj, Abdulaziz Alrehaili, Periyan Durairaju, Mostafizur Rahaman, Govindasami Periyasami, Natarajan Arumugam, Santhakumar Yeswanth Kumar, Ali Aldalbahi, Raju Suresh Kumar
Publikováno v:
Bioorganic chemistry. 88
A series of novel covalent cholesterol-spiro pyrrolidine/pyrrolizidine heterocyclic hybrids possessing biologically active oxindole, indanedione, and acenaphthylene-1-one have been synthesized by the reaction of C3-β-cholesteroalacrylate with hetero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37921ecf09d38cfbb7822a8723f3d7f3
https://pubmed.ncbi.nlm.nih.gov/30991194
https://pubmed.ncbi.nlm.nih.gov/30991194