Add to ORKG3,5,6-, 3,5,7-, 4,5,7-, and 5,6,7-trichloro- and -tribromo-8-quinolinols as well as 3,5,6,7- tetrachloro- and -tetrabromo-8-quinolinols were prepared and tested against six fungi (Aspergillus niger, Aspergillus oryzae, Myrothecium verrucaria, Trichoderma viride, Mucor cirinelloides, and Trichophyton mentagrophytes) in Sabouraud dextrose broth. The compounds strongly inhibit five fungi but not M. cirinelloides. They are less active than the related dichloro-8-quinolinols which is attributed to steric hindranc
A series of new alkyl and arylalkyl ethers of 2-(2,4-dichlorophenyl)-3- (1H-1,2,4-triazol-1-yl)propa...
Antifungal activity of four organic compounds was determined against fungi. Out of these m-chloronit...
A few 5:6- and 5:8-quinoline quinones have been synthesised by oxidising the corresponding aminohydr...
3,5,6-, 3,5,7-, 4,5,7-, and 5,6,7-trichloro- and -tribromo-8-quinolinols as well as 3,5,6,7- tetrach...
3-Bromo-6-chloro- and 6-bromo-3-chloro-8-nitro, -8-amino-, and -8-hydroxyquinolines along with 3-bro...
2,5-, 3,5-, 3,7-, 4,5-, 5,6-, und 6,7-Dichloro-8-quinolinols were prepared and tested along with the...
3,6-Dichloro- and 3,6-dibromo-8-quinolinols were prepared by direct halogenation of 8-nitroquinoline...
A study was made of the fungitoxicity of 2-, 3-, 4-, 5-, 6- and 7-chloro and bromo- 8-quinolinols ag...
Fourteen mono- and dichloro-8-quinolinols were tested against five fungi (Aspergillus niger, A. oryz...
3-Iodo- and 6-Iodo-8-quinolinols were prepared and tested against six fungi: Aspergillus niger, A. o...
Antifungal studies were made of mixtures of minimal inhibitory concentrations (MICs) of 8-quinolinol...
8-Quinolinol-5-sulfonic acid was nearly devoid of antimicrobial activity, due to what was believed t...
6-Fluoro-8-quinolinol was prepared from 2-amino-5-fluorophenol by a Skraup synthesis. No synergism w...
Thirty one compounds (phenol; its 12 possible monohalo analogues; 18 nitrophenols (2- and 4-nitrophe...
Antifungal studies were made of mixtures of minimal inhibitory concentrations (MICs) of 8-quinolinol...
A series of new alkyl and arylalkyl ethers of 2-(2,4-dichlorophenyl)-3- (1H-1,2,4-triazol-1-yl)propa...
Antifungal activity of four organic compounds was determined against fungi. Out of these m-chloronit...
A few 5:6- and 5:8-quinoline quinones have been synthesised by oxidising the corresponding aminohydr...
3,5,6-, 3,5,7-, 4,5,7-, and 5,6,7-trichloro- and -tribromo-8-quinolinols as well as 3,5,6,7- tetrach...
3-Bromo-6-chloro- and 6-bromo-3-chloro-8-nitro, -8-amino-, and -8-hydroxyquinolines along with 3-bro...
2,5-, 3,5-, 3,7-, 4,5-, 5,6-, und 6,7-Dichloro-8-quinolinols were prepared and tested along with the...
3,6-Dichloro- and 3,6-dibromo-8-quinolinols were prepared by direct halogenation of 8-nitroquinoline...
A study was made of the fungitoxicity of 2-, 3-, 4-, 5-, 6- and 7-chloro and bromo- 8-quinolinols ag...
Fourteen mono- and dichloro-8-quinolinols were tested against five fungi (Aspergillus niger, A. oryz...
3-Iodo- and 6-Iodo-8-quinolinols were prepared and tested against six fungi: Aspergillus niger, A. o...
Antifungal studies were made of mixtures of minimal inhibitory concentrations (MICs) of 8-quinolinol...
8-Quinolinol-5-sulfonic acid was nearly devoid of antimicrobial activity, due to what was believed t...
6-Fluoro-8-quinolinol was prepared from 2-amino-5-fluorophenol by a Skraup synthesis. No synergism w...
Thirty one compounds (phenol; its 12 possible monohalo analogues; 18 nitrophenols (2- and 4-nitrophe...
Antifungal studies were made of mixtures of minimal inhibitory concentrations (MICs) of 8-quinolinol...
A series of new alkyl and arylalkyl ethers of 2-(2,4-dichlorophenyl)-3- (1H-1,2,4-triazol-1-yl)propa...
Antifungal activity of four organic compounds was determined against fungi. Out of these m-chloronit...
A few 5:6- and 5:8-quinoline quinones have been synthesised by oxidising the corresponding aminohydr...