Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Krishnan Revathy"'
Publikováno v:
Journal of Graphic Novels & Comics; Feb-Apr2024, Vol. 15 Issue 1, p3-19, 17p
Publikováno v:
Journal of Graphic Novels & Comics; Apr2023, Vol. 14 Issue 2, p300-306, 7p
Autor:
Cinnathambi Subramani Maheswari, Chandrabose Shanmugapriya, Krishnan Revathy, Appaswami Lalitha
Publikováno v:
Journal of Nanostructure in Chemistry, Vol 7, Iss 3, Pp 283-291 (2017)
A new protocol for the synthesis of 2H-indazolo[2,1-b]phthalazine-trione derivatives is described via a one-pot three-component condensation reaction of phthalhydrazide, dimedone or 1,3-cyclohexanedione and aromatic aldehydes catalyzed by SnO2 nanopa
Autor:
Krishnan Revathy, Appaswami Lalitha
Publikováno v:
Journal of the Iranian Chemical Society. 12:2045-2049
p-Toluene sulfonic acid-catalyzed one-pot reaction of anthranilamide with ketones resulted in very good yields of novel spiroquinazolinones. The reaction worked well with a wide variety of ketones in shorter reaction times. The products were characte
Autor:
Krishnan Revathy, Appaswami Lalitha
Publikováno v:
RSC Adv.. 4:279-285
An efficient method for the synthesis of spirooxindolopyrrolizidine/spirooxindolothiapyrrolizidine by the 1,3-dipolar cycloaddition of azomethine ylides generated via, decarboxylative condensation of 1,2-dicarbonyl compounds and L-proline/L-thiaproli
Autor:
Krishnan Revathy, Appaswami Lalitha
Publikováno v:
ChemInform. 46
Autor:
Krishnan Revathy, Appaswami Lalitha
Department of Chemistry, Periyar University, Salem-636 011, Tamilnadu, India E-mail : lalitha2531@yahoo.co.in We have developed a potential method for the synthesis of biologically active1 2,2´-dimethyl-13-phenyl-2,3- dihydro-1H-indazolo[2,1-b]phtha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::333b7d8753c1af0802a7b21f0d52c53b
Autor:
Krishnan Revathy, Appaswami Lalitha
Publikováno v:
ChemInform. 45
An efficient method for the synthesis of spirooxindolopyrrolizidine/spirooxindolothiapyrrolizidine by the 1,3-dipolar cycloaddition of azomethine ylides generated via, decarboxylative condensation of 1,2-dicarbonyl compounds and L-proline/L-thiaproli