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Comparison of ester enolate and silylketene acetal variants of the Ireland Claisen rearrangements in bis-allylic substrates
被引:0
|
作者
:
Nelsen, C
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA
Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA
Nelsen, C
[
1
]
Hong, SP
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA
Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA
Hong, SP
[
1
]
McIntosh, MC
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA
Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA
McIntosh, MC
[
1
]
机构
:
[1]
Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA
来源
:
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
|
1999年
/ 217卷
关键词
:
D O I
:
暂无
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
243-CHED
引用
收藏
页码:U376 / U376
页数:1
相关论文
共 1 条
[1]
Highly stereoselective synthesis of trifluoromethylated compounds via ester-enolate [2,3]-Wittig and [3,3]-Ireland-Claisen rearrangements
Konno, T
论文数:
0
引用数:
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h-index:
0
机构:
TOKYO INST TECHNOL,DEPT BIOENGN,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
TOKYO INST TECHNOL,DEPT BIOENGN,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
Konno, T
Umetani, H
论文数:
0
引用数:
0
h-index:
0
机构:
TOKYO INST TECHNOL,DEPT BIOENGN,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
TOKYO INST TECHNOL,DEPT BIOENGN,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
Umetani, H
Kitazume, T
论文数:
0
引用数:
0
h-index:
0
机构:
TOKYO INST TECHNOL,DEPT BIOENGN,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
TOKYO INST TECHNOL,DEPT BIOENGN,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
Kitazume, T
JOURNAL OF ORGANIC CHEMISTRY,
1997,
62
(01):
: 137
-
150
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