Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Arumugasamy Vanangamudi"'
Autor:
Arumugasamy Vanangamudi, S. Sivasubramanian, Murugaiyan Shanmugam Ramachandran, Alagunambi Ramasubbu, Shanmugam Muthusubramanian
Publikováno v:
Electrochemistry Communications, Vol 2, Iss 1, Pp 56-64 (2000)
A clay-modified electrode (CME) consisting of novel colloidal silver–montmorillonite clay composite material (Ag0n–MM) has been prepared and characterized. The study on its ability to enhance the redox reactions of phenothiazine dyes reveals that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fc9cbc53ff8eb5c05ab5db4f0d0c6c6
https://doi.org/10.1016/s1388-2481(99)00131-9
https://doi.org/10.1016/s1388-2481(99)00131-9
Autor:
Ponnusamy Mohan, M. Thirumalaikumar, Shanmugam Muthusubramanian, Shunmugaperumal Sivasubramanian, Arumugasamy Vanangamudi
Publikováno v:
Synthetic Communications. 29:2013-2017
The a-aryl-N-(β-phenylethyl)nitrones when subjected to SO2Cl2/Et3N and NCS/NaOMe treatment independently, gave unexpectedly the corresponding amides. These procedures form an alternative route for the rearrangement of nitrones to amides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6685dc5c4ab9e152024f35d228dcc2b1
https://doi.org/10.1080/00397919908086190
https://doi.org/10.1080/00397919908086190
Autor:
Ragunathan Priyanka, Kanagasabai Kanagalakshmi, Arumugasamy Vanangamudi, Balasubramanian Hemalatha, Mariappan Premanathan
Publikováno v:
ChemInform. 41
This fast and high yielding method provides the diarylchromanones (III) and methoxyisoflavanone (V) by microwave-assisted condensation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f1e8bd0ad9020ad167acf2d223ea7f8
https://doi.org/10.1002/chin.201041125
https://doi.org/10.1002/chin.201041125
Publikováno v:
ChemInform. 27
The chemical investigation of Tephrosia hookeriana root resulted in the isolation of the new flavone hookerianin characterized as 5,7-dimethoxy-8-[3″-(2″,5″-dihydro-5″,5″-dimethyl-2″-oxofuryl)]-flavone along with (−)semiglabrin and lanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d6910a0b782ee5c15366a45c17126cd
https://doi.org/10.1002/chin.199649257
https://doi.org/10.1002/chin.199649257
Autor:
Arumugasamy Vanangamudi, S. Sivasubramanian, Shanmugam Muthusubramanian, M. Thirumalaikumar, Ponnusamy Mohan
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c283360ddf91a6dec8e2753605d4ad27
https://doi.org/10.1002/chin.199931063
https://doi.org/10.1002/chin.199931063
Autor:
Balasubramanian Hemalatha, Mariappan Premanathan, Kanagasabai Kanagalakshmi, Ragunathan Priyanka, Arumugasamy Vanangamudi
Publikováno v:
European journal of medicinal chemistry. 45(6)
A convenient, fast and high yielding method for the preparation of 7-methoxyisoflavanone and 2,3-diarylchromanones has been developed by the condensation of benzyl-2-hydroxy-4-alkoxyphenylketone with arylaldehyde/paraformaldehyde in presence of dieth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b8edbf983be87c8de437acff8ae1fbc
https://pubmed.ncbi.nlm.nih.gov/20227144
https://pubmed.ncbi.nlm.nih.gov/20227144