Efficient Iron‐Catalyzed Sakurai–Michael Addition of Allyltrimethylsilane to Chalcones-Reference-Cited by-同舟云学术

Efficient Iron‐Catalyzed Sakurai–Michael Addition of Allyltrimethylsilane to Chalcones

Published:2008-03-01 Issue:7 Volume:38 Page:1011-1019
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Xu Li‐Wen¹²,Yang Ming‐Song¹,Qiu Hua‐Yu¹,Lai Guo‐Qiao¹,Jiang Jian‐Xiong¹

Affiliation:

1. a Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University , Hangzhou, 310012, China

2. b State Key Laboratory for Oxosynthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, and Graduate School of the Chinese Academy of Sciences , Lanzhou, China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397910701860646

Reference39 articles.

1. Colvin , E. 1981. Silicon in Organic Synthesis 97London: Butterworth.

2. Weber , W. P. 1983. Silicon Reagents for Organic Synthesis Vol. 12, 173Berlin: Springer‐Verlag.

3. A stereoselective synthesis of (.+-.)-nootkatone and (.+-.)-valencene via an intramolecular Sakurai reaction

4. Characteristics in the reactions of allylsilanes and their applications to versatile synthetic equivalents

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