The oxidation of ketones with a heteropolyacid, H5[PMo 10V2O40] and dioxygen

Bassam El Ali; Jean Marie Brégeault; Jacqueline Mercier; Jacques Martin; Claudine Martin; Odile Convert

doi:10.1039/C39890000825

The oxidation of ketones with a heteropolyacid, H₅[PMo ₁₀V₂O₄₀] and dioxygen

Bassam El Ali
, Jean Marie Brégeault^*
, Jacqueline Mercier
, Jacques Martin
, Claudine Martin
, Odile Convert

^*Corresponding author for this work

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

63 Scopus citations

Abstract

Substituted cycloalkanones, 1-phenylalkanones, and open-chain ketones are oxidatively cleaved by the title compound under very mild conditions.

Original language	English
Pages (from-to)	825-826
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	13
DOIs	https://doi.org/10.1039/C39890000825
State	Published - 1989
Externally published	Yes

ASJC Scopus subject areas

Molecular Medicine

Access to Document

10.1039/C39890000825

Cite this

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title = "The oxidation of ketones with a heteropolyacid, H5[PMo 10V2O40] and dioxygen",

abstract = "Substituted cycloalkanones, 1-phenylalkanones, and open-chain ketones are oxidatively cleaved by the title compound under very mild conditions.",

author = "\{El Ali\}, Bassam and Br{\'e}geault, \{Jean Marie\} and Jacqueline Mercier and Jacques Martin and Claudine Martin and Odile Convert",

year = "1989",

doi = "10.1039/C39890000825",

language = "English",

pages = "825--826",

number = "13",

}

TY - JOUR

T1 - The oxidation of ketones with a heteropolyacid, H5[PMo 10V2O40] and dioxygen

AU - El Ali, Bassam

AU - Brégeault, Jean Marie

AU - Mercier, Jacqueline

AU - Martin, Jacques

AU - Martin, Claudine

AU - Convert, Odile

PY - 1989

Y1 - 1989

N2 - Substituted cycloalkanones, 1-phenylalkanones, and open-chain ketones are oxidatively cleaved by the title compound under very mild conditions.

AB - Substituted cycloalkanones, 1-phenylalkanones, and open-chain ketones are oxidatively cleaved by the title compound under very mild conditions.

UR - https://www.scopus.com/pages/publications/1542573971

U2 - 10.1039/C39890000825

DO - 10.1039/C39890000825

M3 - Article

AN - SCOPUS:1542573971

SN - 0022-4936

SP - 825

EP - 826

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 13