作者:Yu. A. Zhuravleva、A. V. Zimichev、M. N. Zemtsova、Yu. N. Klimochkin
DOI:10.1134/s1070428009040228
日期:2009.4
Reduction of some substituted quinoline-4-carboxylic acids was studied. The reduction of 2-alkylquinoline-4-carboxylic acids with Raney nickel in aqueous alkali was stereoselective, and the resulting 2-alkyl-1,2,3,4-tetrahydroquinoline-4-carboxylic acids were individual cis isomers.