HETERO-RING LITHIATION OF N-METHYL-4-QUINOLONE AND N-METHYLQUINOLINE-4-THIONE

被引:17
作者
ALVAREZ, M
SALAS, M
RIGAT, L
DEVECIANA, A
JOULE, JA
机构
[1] UNIV BARCELONA,FAC PHARM,ORGAN CHEM LAB,E-08028 BARCELONA,SPAIN
[2] UNIV MANCHESTER,DEPT CHEM,MANCHESTER M13 9PL,LANCS,ENGLAND
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1992年 / 03期
关键词
D O I
10.1039/p19920000351
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Lithiation of 1-methyl-4-quinolone and 1-methylquinoline-4-thione with lithium diisopropylamide (LDA) at -78-degrees-C takes place at C-2. The resulting lithio-species react with a variety of electrophiles to give 2-substituted-4-quinolones and -quinolines-4-thiones respectively. 1-Methylquinoline-4-thione is easily converted into 1-methyl-4-quinolone in protic solution.
引用
收藏
页码:351 / 356
页数:6
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