Oxidative Double Bond Cleavage of α-Substituted Styrenes with Molecular Oxygen-Reference-Cited by-同舟云学术

Oxidative Double Bond Cleavage of α-Substituted Styrenes with Molecular Oxygen

Published:2002-03-01 Issue:3 Volume:31 Page:414-415
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:

Author:

Hayashi Yujiro¹,Takeda Mitsuhiro¹,Miyamoto Yuji¹,Shoji Mitsuru¹

Affiliation:

1. Department of Industrial Chemistry, Faculty of Engineering, Science University of TokyoKagurazaka, Shinjuku-ku, Tokyo

Abstract

Abstract Oxidative cleavage of the carbon-carbon double bond of α-substituted styrene derivatives proceeds under an atmospheric pressure of molecular oxygen at the solventless conditions to afford the corresponding ketones in moderate yields with no requirement for transition metal catalysts or photo-activation.

Publisher

Oxford University Press (OUP)

Link

https://academic.oup.com/chemlett/article-pdf/31/3/414/55578132/cl.2002.414.pdf

Reference38 articles.

1. New and Effective Aerobic Oxygenation of Olefins Catalyzed by Transition-Metal Complexes.

2. Development of Novel Aerobic Oxidation Method using N-Hydroxyphthalimide as Catalyst

3. Green, Catalytic Oxidation of Alcohols in Water

4. Palladium(II)-Catalyzed Oxidation of Alcohols to Aldehydes and Ketones by Molecular Oxygen

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