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Preparation of 2,3-epoxycycloalkanones from bicyclo [n.1.0]alkan-1-ols
被引:15
|
作者
:
Barnier, JP
论文数:
0
引用数:
0
h-index:
0
机构:
CNRS, Inst Chim Mol Orsay, Lab Carbocycles, F-91405 Orsay, France
CNRS, Inst Chim Mol Orsay, Lab Carbocycles, F-91405 Orsay, France
Barnier, JP
[
1
]
Morisson, V
论文数:
0
引用数:
0
h-index:
0
机构:
CNRS, Inst Chim Mol Orsay, Lab Carbocycles, F-91405 Orsay, France
CNRS, Inst Chim Mol Orsay, Lab Carbocycles, F-91405 Orsay, France
Morisson, V
[
1
]
Blanco, L
论文数:
0
引用数:
0
h-index:
0
机构:
CNRS, Inst Chim Mol Orsay, Lab Carbocycles, F-91405 Orsay, France
CNRS, Inst Chim Mol Orsay, Lab Carbocycles, F-91405 Orsay, France
Blanco, L
[
1
]
机构
:
[1]
CNRS, Inst Chim Mol Orsay, Lab Carbocycles, F-91405 Orsay, France
来源
:
SYNTHETIC COMMUNICATIONS
|
2001年
/ 31卷
/ 03期
关键词
:
D O I
:
10.1081/SCC-100000523
中图分类号
:
O62 [有机化学];
学科分类号
:
070303 ;
081704 ;
摘要
:
Copper- or iron-catalyzed oxidative rearrangement of bicyclo[n.1.0]alkan-1-ols yields 3-hydroperoxycycloalkanones and/or bicyclic peroxyhemiketals, which are transformed into 2,3-epoxy-cycloalkanones by treatment with a base.
引用
收藏
页码:349 / 357
页数:9
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