Oxidative double bond cleavage of α-substituted styrenes with molecular oxygen

Yujiro Hayashi; Mitsuhiro Takeda; Yuji Miyamoto; Mitsuru Shoji

doi:10.1246/cl.2002.414

Oxidative double bond cleavage of α-substituted styrenes with molecular oxygen

Yujiro Hayashi, Mitsuhiro Takeda, Yuji Miyamoto, Mitsuru Shoji

Research output: Contribution to journal › Article › peer-review

24 Citations (Scopus)

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.

Original language	English
Pages (from-to)	414-415
Number of pages	2
Journal	Chemistry Letters
Issue number	3
DOIs	https://doi.org/10.1246/cl.2002.414
Publication status	Published - 2002 Mar 5
Externally published	Yes

ASJC Scopus subject areas

Chemistry(all)

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10.1246/cl.2002.414

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title = "Oxidative double bond cleavage of α-substituted styrenes with molecular oxygen",

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.",

author = "Yujiro Hayashi and Mitsuhiro Takeda and Yuji Miyamoto and Mitsuru Shoji",

year = "2002",

month = mar,

day = "5",

doi = "10.1246/cl.2002.414",

language = "English",

pages = "414--415",

journal = "Chemistry Letters",

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T1 - Oxidative double bond cleavage of α-substituted styrenes with molecular oxygen

AU - Hayashi, Yujiro

AU - Takeda, Mitsuhiro

AU - Miyamoto, Yuji

AU - Shoji, Mitsuru

PY - 2002/3/5

Y1 - 2002/3/5

N2 - 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.

AB - 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.

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U2 - 10.1246/cl.2002.414

DO - 10.1246/cl.2002.414

M3 - Article

AN - SCOPUS:0036012164

SN - 0366-7022

SP - 414

EP - 415

JO - Chemistry Letters

JF - Chemistry Letters

IS - 3

ER -

Oxidative double bond cleavage of α-substituted styrenes with molecular oxygen

Abstract

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