Zobrazeno 1 - 10
of 86
pro vyhledávání: '"B. China Raju"'
Autor:
K. Suchitra Rani, S. Ramya, K. S. Hariprasad, G. Praveena, A. Zehra, R. S. Prakasham, A. K. Tiwari, B. China Raju
Publikováno v:
Russian Journal of Bioorganic Chemistry. 47:1335-1340
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e392097442ca9ca9764811187388aecc
https://doi.org/10.1134/s1068162021060224
https://doi.org/10.1134/s1068162021060224
Akademický článek
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Publikováno v:
Medicinal Chemistry Research. 29:217-228
The present study is aimed to synthesize the novel 7-hydroxyflavanone derived compounds and to assess their biological activity. Two series of compounds such as 2-phenyl-7-((3-phenylisoxazol-5-yl)methoxy)chroman-4-ones (6a–h) and 4-oxo-2-phenylchro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5a6e7fa09cb7ce32e87ac5fc7296066
https://doi.org/10.1007/s00044-019-02476-5
https://doi.org/10.1007/s00044-019-02476-5
Publikováno v:
Asian Journal of Organic Chemistry. 8:1380-1384
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf517603865c8b97c05f388daf0b05ba
https://doi.org/10.1002/ajoc.201900296
https://doi.org/10.1002/ajoc.201900296
Publikováno v:
Russian Journal of General Chemistry. 86:2900-2905
The present study deals with conventional Witting olefination of 2H-chromene-3-carbaldehydes with stabilized ylide in the presence of dichloromethane to afford (2E)-ethyl-3-(4-chloro-2H-chromen-3-yl) acrylate derivatives. All the products were found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c7fbf2897d3a7c3938080f2ace2295c
https://doi.org/10.1134/s1070363216120586
https://doi.org/10.1134/s1070363216120586
Autor:
Ashita Singh, B. China Raju, Gannerla Saidachary, D. Divya, K. Veera Prasad, Balasubramanian Sridhar, U. Ramesh
Publikováno v:
European Journal of Medicinal Chemistry. 76:460-469
Series of new benzoxepinoisoxazolones 4a – d and pyrazolones 6a – t were prepared by the cyclocondensation of substituted ( E )-ethyl 3-oxo-2,3-dihydrobenzo[ b ]oxepine-4-carboxylates 3a – d with hydroxylamine hydrochloride and phenylhydrazine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a90941c8b867a548e207a93ce3f8ac3d
https://doi.org/10.1016/j.ejmech.2014.02.042
https://doi.org/10.1016/j.ejmech.2014.02.042
Autor:
Anthony Addlagatta, D. Anand Kumar, Zehra Ali, Gannerla Saidachary, Ashok Kumar Tiwari, J. Ashok Kumar, B. China Raju, Balasubramanian Sridhar, Chandan Kishor
Publikováno v:
Medicinal Chemistry Research. 23:2821-2833
Pyranochromenone derivatives 3a–d, 6a–j and 2H-chromenones 8a–b were synthesized and screened for their in vitro α-amylase inhibitory and ABTS•+ [2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)] free radical scavenging activities. C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::478f6b3b7034bad6ccd4ccfcd07caf63
https://doi.org/10.1007/s00044-013-0867-y
https://doi.org/10.1007/s00044-013-0867-y
Publikováno v:
Tetrahedron Letters. 52:4985-4988
Alkenylalumination of aldehydes with [α-(ethoxycarbonyl)-β-(t-butyldimethylsilyloxyalkyl)alkenyl]diisobutylaluminum provides the corresponding α-Z-alkylidene-β′-hydroxy esters, which upon protection and treatment with trifluoroacetic acid lacto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b714096a7222c716213109bcff91d16
https://doi.org/10.1016/j.tetlet.2011.06.103
https://doi.org/10.1016/j.tetlet.2011.06.103
Publikováno v:
Journal of Heterocyclic Chemistry. 48:1251-1257
Series of phosphorylated coumarin derivatives (4a, 4b, 4c, 4d, 4e, 4f, 4g, 4h, 4i, 4j) were synthesized by Pechmann condensation, phosphorylation, and debenzylation reactions in very good yields. Thus, synthesized compounds (4a, 4b, 4c, 4d, 4e, 4f, 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da8eda939fce18dc7ca64ffdbc732943
https://doi.org/10.1002/jhet.675
https://doi.org/10.1002/jhet.675
Publikováno v:
Journal of Heterocyclic Chemistry. 46:1213-1217
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b33b4fe92f16a0c152cc3d586507384a
https://doi.org/10.1002/jhet.208
https://doi.org/10.1002/jhet.208