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Aldehyde addition to allylic stannanes via a transmetallation pathway: Stereocontrol in the absence of internal coordination
被引:0
|
作者
:
Marshall, Raymond L.
论文数:
0
引用数:
0
h-index:
0
机构:
School of Science, Griffith University, Nathan, QLD 4111, Australia
School of Science, Griffith University, Nathan, QLD 4111, Australia
Marshall, Raymond L.
[
1
]
Muderawan, I. Wayan
论文数:
0
引用数:
0
h-index:
0
机构:
School of Science, Griffith University, Nathan, QLD 4111, Australia
School of Science, Griffith University, Nathan, QLD 4111, Australia
Muderawan, I. Wayan
[
1
]
Young, David J.
论文数:
0
引用数:
0
h-index:
0
机构:
School of Science, Griffith University, Nathan, QLD 4111, Australia
School of Science, Griffith University, Nathan, QLD 4111, Australia
Young, David J.
[
1
]
机构
:
[1]
School of Science, Griffith University, Nathan, QLD 4111, Australia
来源
:
Journal of the Chemical Society. Perkin Transactions 2
|
2000年
/ 05期
关键词
:
Allylic stannanes - Electrophile - Indium chloride - Lewis acids - Methyltin trichloride - Regiochemistry - Stereocontrol - Stereoelectronic factors - Steric factors - Transmetallation;
D O I
:
10.1039/b000435i
中图分类号
:
学科分类号
:
摘要
:
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收藏
页码:957 / 962
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[1]
Aldehyde addition to allylic stannanes via a transmetallation pathway:: stereocontrol in the absence of internal coordination
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引用数:
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Griffith Univ, Sch Sci, Nathan, Qld 4111, Australia
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[2]
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Addition reaction of allylic stannanes to the triplet excited state of C-60 via photoinduced electron transfer process leading to asymmetric hybridization chemistry for fullerene terpenoid
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