Register      Login
Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science

Articles citing this paper

Potential Antimalarials. VIII. Mono- and Di-mannich Bases of 2-(7′-Trifluoro-methylquinolin-4′-ylamino)phenol Via 2-Nitrophenols

GB Barlin and JH Yan
42(12) pp.2191 - 2199


3 articles found in Crossref database.

Thein vitroandin vivoantimalarial activity of some Mannich bases derived from 4-(7′-trifluoromethyl-1′,5′-naphthyridin-4′-ylamino)phenol, 2-(7′-trifluoromethyl-quinolin-4′-ylamino)phenol, and 4′-chloro-5-(7″-trifluoromethylquinolin-4″-ylamino)biphenyl-2-ols
Barlin G. B., Jiravinyu Chuenjit, Butcher G. A, Kotecka Barbara, Rieckmann K.
Annals of Tropical Medicine & Parasitology. 1992 86(4). p.323
New quinoline di-Mannich base compounds with greater antimalarial activity than chloroquine, amodiaquine, or pyronaridine
Kotecka B M, Barlin G B, Edstein M D, Rieckmann K H
Antimicrobial Agents and Chemotherapy. 1997 41(6). p.1369
ChemInform Abstract: Potential Antimalarials. Part 8. Mono‐ and Di‐Mannich Bases of 2‐(7′‐Trifluoromethylquinolin‐4′‐ylamino)phenol via 2‐Nitrophenols.
BARLIN G. B., YAN J.‐H.
ChemInform. 1990 21(16).

Committee on Publication Ethics


Abstract Export Citation Get Permission