Naphthoquinone antimalarials. XIV. 2-Hydroxy-3-aryl-1, 4-naphthoquinones
HE Zaugg, RT Rapala, MT Leffler
Index: Zaugg; Rapala; Leffler Journal of the American Chemical Society, 1948 , vol. 70, p. 3224,3226
Full Text: HTML
Citation Number: 16
Abstract
The observation'that 2-hydroxy-3-phenyl-l, 4-ported that p-chlorophenylacetic ester gave the naphthoquinone2 (IV, R1= Rz= Rs= H) has an corresponding/3-keto-ester (11) in good yield with activity approximately one-fourth that of quinine isopropylmagnesium bromide as a catalyst5 but against P. lophurae in ducks, prompted further in-did not react in the presence of sodium ethoxide. vestigation in this series. Therefore the former reagent was chosen for ...
Related Articles:
Reformatsky type additions of haloacetonitriles to aldehydes mediated by metallic nickel
[Inaba, Shin-ichi; Rieke, Reuben D. Chemistry Letters, 1984 , p. 25 - 28]
Nickel catalyzed electrosynthesis of ketones from organic halides and metal carbonyls
[Dolhem; Ocafrain; Nedelec; Troupel Tetrahedron, 1997 , vol. 53, # 50 p. 17089 - 17096]