Regioselective Addition of Silyl Enolates to α,β-Unsaturated Aldehyde and its Acetal Catalyzed by MgI2 Etherate

Xing Xian ZHANG Wei Dong Z. LI

引用本文: Xing Xian ZHANG,  Wei Dong Z. LI. Regioselective Addition of Silyl Enolates to α,β-Unsaturated Aldehyde and its Acetal Catalyzed by MgI2 Etherate[J]. Chinese Chemical Letters, 2003, 14(8): 800-803. shu
Citation:  Xing Xian ZHANG,  Wei Dong Z. LI. Regioselective Addition of Silyl Enolates to α,β-Unsaturated Aldehyde and its Acetal Catalyzed by MgI2 Etherate[J]. Chinese Chemical Letters, 2003, 14(8): 800-803. shu

Regioselective Addition of Silyl Enolates to α,β-Unsaturated Aldehyde and its Acetal Catalyzed by MgI2 Etherate

  • 基金项目:

    We are grateful for the financial supports from the National Outstanding Youth Fund (No.29925204), the Foundation for University Key Teacher by the Ministry of Education of China, and a Visiting Fund of the National Laboratory of Applied Organic Chemistry.

摘要: Regioselective addition reactions of silyl enolates to α,β-unsaturated aldehyde and its acetal catalyzed by MgI2 etherate give aldol adducts (1, 2-addition) preferentially over Michael adducts (1, 4-addition). This unique regioselectivity is distinctly different with other Lewis acidic promoters and may be attributed to the high oxyphilicity of IMg+.

English

  • 加载中
计量
  • PDF下载量:  0
  • 文章访问数:  0
  • HTML全文浏览量:  0
文章相关
  • 收稿日期:  2002-11-04
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

/

返回文章