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Chelating phosphines with C2 and C3 symmetry
被引:10
|
作者
:
Brulé, E
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
Brulé, E
[
1
]
Pei, YX
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
Pei, YX
[
1
]
Lake, F
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
Lake, F
[
1
]
Rahm, F
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
Rahm, F
[
1
]
Moberg, C
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
Moberg, C
[
1
]
机构
:
[1]
Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
来源
:
MENDELEEV COMMUNICATIONS
|
2004年
/ 14卷
/ 06期
关键词
:
D O I
:
10.1070/MC2004v014n06ABEH002026
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
Antide formation between ring opened aziridines and 2-(diphenylphosphino)benzoic acid provides an easy access to chelating di- and triphosphines with C-2 and C-3 symmetry.
引用
收藏
页码:276 / 277
页数:2
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