P(i-PrNCH2CH2)3N: Efficient Catalyst for Synthesizing β-Hydroxyesters and α,β-Unsaturated Esters using α-Trimethylsilylethylacetate (TMSEA)

被引:45
|
作者
Wadhwa, Kuldeep [1 ]
Verkade, John G. [1 ]
机构
[1] Iowa State Univ, Dept Chem, Ames, IA 50011 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2009年 / 74卷 / 11期
基金
美国国家科学基金会;
关键词
WITTIG OLEFINATION REACTION; REFORMATSKY-TYPE REACTIONS; CARBONYL-COMPOUNDS; ORGANIC-SYNTHESIS; ACTIVATED METALS; ALDOL REACTION; KETONES; ALDEHYDES; ETHERS; ACIDS;
D O I
10.1021/jo900477q
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We present an efficient synthesis of beta-hydroxyesters and alpha,beta-unsaturated esters via activation of the silicon-carbon bond of alpha-trimethylsilylethyl acetate using catalytic amounts of the commercially available P(i-PrNCH2CH2)(3)N 1a. Selectivity for either of these two products can be achieved simply by altering the catalyst loading and reaction temperature to afford addition or stereoselective condensation. This method is mild and tolerates a wide array of functional groups.
引用
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页码:4368 / 4371
页数:4
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