Efficient and Stereoselective Rearrangement of Baylis-Hillman Acetates Catalyzed by Gold(I) Chloride/Silver(I) Trifluoromethanesulfonate-Reference-Cited by-同舟云学术

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Efficient and Stereoselective Rearrangement of Baylis-Hillman Acetates Catalyzed by Gold(I) Chloride/Silver(I) Trifluoromethanesulfonate

Published:2009-02-24 Issue:07 Volume:2009 Page:1170-1174
ISSN:0039-7881
Container-title:Synthesis
language:en
Short-container-title:Synthesis

Author:

Xu Zhenyuan,Liu Yunkui,Mao Dajie,Qian Jianqiang,Lou Shaojie,Zhang Yongmin

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0028-1087971.pdf

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. NaNO₂-catalyzed reaction of cyclohexenone-MBH acetates: A convenient synthesis of 2-methylene-3-cyclohexenones;Synthetic Communications;2023-07-14

2. The Gold(I)- and Silver(I)-Catalyzed Nicholas Reaction;Organometallics;2013-02-01

3. Palladium-catalyzed arylation of methyl 2-(acetoxymethyl)acrylate: a convenient synthesis of rearranged Morita–Baylis–Hillman acetates;Tetrahedron Letters;2013-01

4. Sodium tetrachloroaurate(III) dihydrate-catalyzed efficient synthesis of 1,5-benzodiazepine and quinoxaline derivatives;Journal of Zhejiang University SCIENCE B;2010-02

5. Gold(III)-Catalyzed Tandem Reaction of Ketones with Phenols: Efficient and Highly Selective Synthesis of Functionalized 4H-Chromenes;The Journal of Organic Chemistry;2010-01-14

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