Asymmetric Morita-Baylis-Hillman Reaction Catalyzed by Simple Amino Alcohol Derived Thioureas

Asymmetric Morita-Baylis-Hillman Reaction Catalyzed by Simple Amino Alcohol Derived Thioureas
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简单氨基醇硫脲催化的不对称 Morita-Baylis-Hillman 反应

DOI:
10.1055/s-2007-984882
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发表时间:
2007
期刊:
影响因子:
2
通讯作者:
A. Lattanzi
A. Lattanzi
中科院分区:
化学4区
文献类型:
--
作者:
A. Lattanzi

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已发现直接衍生自市售对映体纯氨基醇的硫脲促进2-环己烯-1-酮和不同醛在三乙胺存在下在无溶剂条件下的不对称Morita-Baylis-Hillman反应。相应的烯丙醇得到了良好的高产率和高达88%ee。
Thioureas straightforwardly derived from commercially available enantiopure amino alcohols have been found to promote the asymmetric Morita-Baylis-Hillman reaction of 2-cyclohexen-1-one and different aldehydes in the presence of triethylamine under solvent-free conditions. The corresponding allylic alcohols were obtained in good to high yields and up to 88% ee.