Palladium-Catalyzed Selenoacylation of Allenes Leading to the Regioselective Formation of Functionalized Allyl Selenides-Reference-Cited by-同舟云学术

Palladium-Catalyzed Selenoacylation of Allenes Leading to the Regioselective Formation of Functionalized Allyl Selenides

Published:2008-08-21 Issue:18 Volume:10 Page:3957-3960
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Toyofuku Masashi¹,Murase Erika¹,Fujiwara Shin-ichi¹,Shin-ike Tsutomu¹,Kuniyasu Hitoshi¹,Kambe Nobuaki¹

Affiliation:

1. Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan, and Department of Chemistry, Osaka Dental University, Hirakata, Osaka 573-1121, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol801329q

Reference43 articles.

1. Some Typical Advances in the Synthetic Applications of Allenes

2. Transition Metal-Catalyzed/Mediated Reaction of Allenes with a Nucleophilic Functionality Connected to the α-Carbon Atom

3. Modern Allene Chemistry

4. A highly regioselective bisselenation of allenes with diphenyl diselenide catalyzed by tetrakis(triphenylphosphine)palladium(0)

5. Syntheses and Synthetic Applications of Stannylated Allylic Alcohols

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