STEREOSELECTIVE ALKYLATION OF CYCLIC AND ACYCLIC CHIRAL BETA-ENAMINO KETONES LITHIUM DIANIONS - SYNTHESIS OF EITHER (R)-CHIRAL OR (S)-CHIRAL 1,3-DIKETONES

被引:21
作者
BARTOLI, G
BOSCO, M
CIMARELLI, C
DALPOZZO, R
DEMUNNO, G
PALMIERI, G
机构
[1] DIPARTIMENTO SCI CHIM,VIA S AGOSTINO 1,I-62032 CAMERINO,ITALY
[2] DIPARTIMENTO CHIM ORGAN A MANGINI,I-40136 BOLOGNA,ITALY
[3] UNIV CALABRIA,DIPARTIMENTO CHIM,I-87030 ARCAVACATA,ITALY
关键词
D O I
10.1016/S0957-4166(00)80373-0
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis of either (R)- or (S)-chiral 1,3-diketones through asymmetric gamma alkylation reaction of cyclic and acyclic chiral beta-enamino ketones was here performed. The alkylation takes place with good yields and high d.e. in HMPA/THF. Both the pure enantiomers of 1,3-diketones can be formed by simple hydrolysis of the epimeric beta-enamino ketones obtained with this method, choosing the suitable synthetic strategies. An explanation of the asymmetric induction was proposed.
引用
收藏
页码:1651 / 1665
页数:15
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