Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Saeed Mohammadzadeh Talesh"'
Publikováno v:
Journal of Fluorine Chemistry. 141:11-15
A highly efficient one-pot three-component regioselective synthesis of 2-amino-3-cyano-4 H -chromene and tetrahydrobenzo[ b ]pyran derivatives has been developed by annulation of aldehydes, malononitrile, and resorcinol or dimedone under reflux condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b05e0a5f8d7bd534ee9460c9b7fff55c
https://doi.org/10.1016/j.jfluchem.2012.05.014
https://doi.org/10.1016/j.jfluchem.2012.05.014
Publikováno v:
Comptes Rendus Chimie. 15:779-783
Trifluoroethanol (TFE) is found to be an efficient and recyclable medium in promoting one-pot, three-component coupling reactions of isatoic anhydride, aldehyde and ammonium acetate or primary amine to afford the corresponding 2,3-dihydroquinazolin-4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c259a20435edfb85c5beafaf98e8e301
https://doi.org/10.1016/j.crci.2012.05.019
https://doi.org/10.1016/j.crci.2012.05.019
Publikováno v:
Journal of Fluorine Chemistry. 140:95-98
A simple and convenient procedure for the oxidation of various benzylic, allylic and some aliphatic alcohols to their corresponding carbonyl compounds is described using sodium hypochlorite as the oxidant in 1,1,1,3,3,3-hexafluoro-2-propanol without
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::770fb55ffcd72cf97dbf4c67516421a4
https://doi.org/10.1016/j.jfluchem.2012.05.017
https://doi.org/10.1016/j.jfluchem.2012.05.017
Publikováno v:
Journal of Fluorine Chemistry. 136:8-11
Hexafluoro-2-propanol (HFIP) is explored as an effective medium for the synthesis of symmetrical tris(indolyl)methanes through the reaction of indole derivatives with orthoesters at room temperature. The solvent (HFIP) can be readily separated from r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c83a3850e2bb908388403e4dd6721b6
https://doi.org/10.1016/j.jfluchem.2012.01.002
https://doi.org/10.1016/j.jfluchem.2012.01.002
Publikováno v:
Journal of Fluorine Chemistry. 135:87-90
A simple, inexpensive, environmentally friendly and efficient route for the synthesis of bis-indolyl methanes derivatives by the reaction of indole or N -methyl indole with aldehydes using hexafluoroisopropanol as a solvent is described. The solvent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bded182d7ab4ad4955f3c5f82ec2779
https://doi.org/10.1016/j.jfluchem.2011.09.001
https://doi.org/10.1016/j.jfluchem.2011.09.001
Publikováno v:
ChemInform. 43
A highly efficient one-pot three-component regioselective synthesis of 2-amino-3-cyano-4 H -chromene and tetrahydrobenzo[ b ]pyran derivatives has been developed by annulation of aldehydes, malononitrile, and resorcinol or dimedone under reflux condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2882b320930e03f3a370dd66a3b1fbac
https://doi.org/10.1002/chin.201249146
https://doi.org/10.1002/chin.201249146
Publikováno v:
ChemInform. 43
The oxidation of various benzylic, allylic and some aliphatic alcohols (I), (III), (V) and (VII) to their corresponding carbonyl compounds (II), (IV), (VI) and (VIII) using NaOCl as the oxidant in hexafluoroisopropanol is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ebd7fb47bbd24312f93f3bdefda58dd
https://doi.org/10.1002/chin.201245041
https://doi.org/10.1002/chin.201245041
Publikováno v:
ChemInform. 43
The reaction of orthoesters (II) and (V) with indoles (I) and (IV) is performed in the non-toxic and reusable hexafluoroisopropanol medium to afford the pure tris(indolyl)methanes (III) and (VI), resp., in high yields and short reaction times.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfd8abe9ffa73cccb2a6a2f6f67e1bc5
https://doi.org/10.1002/chin.201233126
https://doi.org/10.1002/chin.201233126
Publikováno v:
ChemInform. 43
Condensation of aldehydes (II) with indoles (I) and (VII) provides the bis-indolyl methanes (III) and (VIII), resp., in high yields without formation of any side products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0b7e35e04dd3bcbfa05089daeff7ce8
https://doi.org/10.1002/chin.201231105
https://doi.org/10.1002/chin.201231105