CHANGE OF REGIOSELECTIVITY IN THE REACTION OF TIN ENOLATES AND ALPHA-BROMO KETONES - SYNTHESIS OF 1,4-DIKETONES UNDER NONRADICAL CONDITIONS
被引:25
作者:
BABA, A
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机构:Department of Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565
BABA, A
YASUDA, M
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机构:Department of Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565
YASUDA, M
YANO, K
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机构:Department of Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565
YANO, K
SHIBATA, I
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h-index: 0
机构:Department of Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565
SHIBATA, I
MATSUDA, H
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机构:Department of Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565
MATSUDA, H
机构:
[1] Department of Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565
来源:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
|
1990年
/
11期
关键词:
D O I:
10.1039/p19900003205
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The reaction of tin enolates with α-halogeno ketones, strikingly effected by the addition of phosphine oxides to the reaction mixture, produced 1,4-diketones under mild conditions; the addition was shown to proceed in a non-radical manner.