This submission belongs to the session a. General Organic Synthesis of the event The 4th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Sep, 2000
Citation
Sakae Uemura, Masashi Inoue, Takahiro Nishimura, Nobuyuki Kakiuchi, Palladium(II) Supported by Hydrotalcite[Pd(II)-Hydrotalcite]-Catalyzed Selective Oxidation of Alcohols Using Molecular Oxygen, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-4-01808
Share
Email
Facebook
Twitter
LinkedIn
Palladium(II) Supported by Hydrotalcite[Pd(II)-Hydrotalcite]-Catalyzed Selective Oxidation of Alcohols Using Molecular Oxygen
Nobuyuki Kakiuchi 1
Takahiro Nishimura 1
Masashi Inoue 1
Sakae Uemura 1
1. Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan
Abstract
Novel heterogenized Pd catalyst, palladium supported by hydrotalcite[Pd(II)-hydrotalcite], has been synthesized. The catalyst is found to be effective for the oxidation of a wide range of alcohols using molecular oxygen as a sole oxidant. In this catalytic system, various alcohols are readily converted to the corresponding aldehydes or ketones selectively in high to excellent yields. It is noteworthy that the catalyst is also applicable to the oxidation of unsaturated alcohols such as geraniol and nerol without any isomerization of an alkenic part. Another characteristic property of this heterogeneous catalyst is that a shape selectivity depending on the structure of alcohols is observed in some extent. The catalyst has also advantages such as ease of handling, easy preparation, and reusability for several times without appreciable loss of the catalytic activity.
Keywords
n/a
Base promoted isomerization of aziridinyl ethers: a new access to a- and b-aminoacids
Synthesis And Electrophilic Substitution of Pyrido[2,3,4-kl]acridines