A stereoselective, tandem [2+2] photocycloaddition-hydrolysis route to aldol-type adducts
被引:20
作者:
Abe, M
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机构:
Osaka Univ, Fac Engn, Dept Chem Mat, Suita, Osaka 5650871, JapanOsaka Univ, Fac Engn, Dept Chem Mat, Suita, Osaka 5650871, Japan
Abe, M
[1
]
Ikeda, M
论文数: 0引用数: 0
h-index: 0
机构:
Osaka Univ, Fac Engn, Dept Chem Mat, Suita, Osaka 5650871, JapanOsaka Univ, Fac Engn, Dept Chem Mat, Suita, Osaka 5650871, Japan
Ikeda, M
[1
]
Nojima, M
论文数: 0引用数: 0
h-index: 0
机构:
Osaka Univ, Fac Engn, Dept Chem Mat, Suita, Osaka 5650871, JapanOsaka Univ, Fac Engn, Dept Chem Mat, Suita, Osaka 5650871, Japan
Nojima, M
[1
]
机构:
[1] Osaka Univ, Fac Engn, Dept Chem Mat, Suita, Osaka 5650871, Japan
来源:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
|
1998年
/
19期
关键词:
D O I:
10.1039/a805404e
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Photocycloadditions of aromatic aldehydes 2a-e With cyclic ketene silyl acetals 1a-e have been investigated. Regio- and exo-selective formation of the bicyclic 2-alkoxyoxetanes 3 was observed in high yields. Hydrolysis of the acidlabile oxetanes 3 with neutral water was efficiently achieved to give aldol type adducts 4 (threo-selective formations).