Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kripalaya Ratheesh, Arya"'
Autor:
Kripalaya Ratheesh, Arya1 (AUTHOR), Karnam Jayarampillai, Rajendra Prasad1 (AUTHOR) prasad_125@yahoo.com
Publikováno v:
ChemistrySelect. 4/30/2020, Vol. 5 Issue 16, p4898-4904. 7p.
Autor:
Kripalaya Ratheesh Arya, Karnam Jayarampillai Rajendra Prasad, Hazel A. Sparkes, Baskaran Vijaya Pandiyan
Publikováno v:
ChemistrySelect. 4:9540-9549
An unprecedented amine-catalyzed stereoselective reaction of α,α-dicyanomethylidenecarbazoles with indane-1,3-dione and aryl/heteroaryl aldehydes afforded a series of indanedione-fused benzo[a]carbazoles. The plausible mechanism for the formation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddc6abb9ef42c96498cbce6c59ff45e0
Publikováno v:
Arya, K R, Sparkes, H A & Prasad, K J P R 2018, ' An efficient one-pot synthesis of carbazole fused benzoquinolines and pyridocarbazoles ', Journal of Chemical Sciences, vol. 130, no. 4, 41 . https://doi.org/10.1007/s12039-018-1428-1
A one-pot, solvent-free protocol for the synthesis of chloro-substituted benzoquinoline-carbazole derivatives via a modified Friedlander hetero-annulation reaction between 2, 3, 4, 9-tetrahydrocarbazol-1-one and 3-amino-2-naphthoic acid in the presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d43265131211e8abf24ee9d2f48c489
https://hdl.handle.net/1983/663e3add-9da6-4d66-b9ff-b77fd4dc2e4b
https://hdl.handle.net/1983/663e3add-9da6-4d66-b9ff-b77fd4dc2e4b
A solvent-free, one-pot, and operationally simple protocol was adopted to synthesize a new series of multifunctionalized pyrido[2,3-a]carbazole derivatives which were structurally characterized by FTIR, 1H-NMR, 13C-NMR, and elemental analysis. The sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c0751d7d4ba9406edd51d3c6e62e996
Publikováno v:
ChemInform. 46
A facile, efficient, three-component reaction of 2,3,4,9-tetrahydro-1H-carbazol-1-one, malononitrile, and aromatic/heteroaromatic aldehydes in dimethylformamide (DMF) gave pyrano[2,3-a]carbazoles in good yields, at reflux condition, using a catalytic
A facile and efficient, three-component reaction of 2,3,4,9-tetrahydro-1H-carbazol-1-one, malononitrile and aromatic/heteroaromatic aldehydes in DMF to give pyrano[2,3-a] carbazoles, in high yields, at reflux condition, using a catalytic amount of pi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::689534aec5c7aae7f13ac2dedd9e70f7
Publikováno v:
Organic & Biomolecular Chemistry; 4/14/2018, Vol. 16 Issue 14, p2527-2540, 14p