A highly efficient enantioselective synthesis of 2-methyl chromans via four sequential palladium-catalyzed reactions

被引:14
|
作者
Palucki, M [1 ]
Yasuda, N [1 ]
机构
[1] Merck & Co Inc, Dept Proc Res, Rahway, NJ 07065 USA
关键词
palladium; chroman; asymmetric;
D O I
10.1016/j.tetlet.2004.12.043
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An enantioselective synthesis of substituted 2-methyl chromans was accomplished in four steps using four sequential Pd-catalyzed reactions. A study of the key palladium-catalyzed regioselective aryl ether ring fort-nation of two different substrates was also carried out to better understand the factors which affect the selectivity of the reaction. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:987 / 990
页数:4
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