Volume 28, Issue 15
Heterocyclic Compounds
Full Access

ChemInform Abstract: A Practical Method for Epoxidation of Terminal Olefins with 30% Hydrogen Peroxide under Halide-Free Conditions.

K. SATO

K. SATO

Dep. Chem. Mol. Chirality Res. Unit., Nagoya Univ., Chikusa, Nagoya 464-01, Japan

Search for more papers by this author
M. AOKI

M. AOKI

Dep. Chem. Mol. Chirality Res. Unit., Nagoya Univ., Chikusa, Nagoya 464-01, Japan

Search for more papers by this author
M. OGAWA

M. OGAWA

Dep. Chem. Mol. Chirality Res. Unit., Nagoya Univ., Chikusa, Nagoya 464-01, Japan

Search for more papers by this author
T. HASHIMOTO

T. HASHIMOTO

Dep. Chem. Mol. Chirality Res. Unit., Nagoya Univ., Chikusa, Nagoya 464-01, Japan

Search for more papers by this author
R. NOYORI

R. NOYORI

Dep. Chem. Mol. Chirality Res. Unit., Nagoya Univ., Chikusa, Nagoya 464-01, Japan

Search for more papers by this author
First published: 04 August 2010

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

The title method works without the use of organic solvents under phase transfer conditions. Aliphatic olefins (Ia)-(Ic) are epoxidated in high yields, whereas styrene (Id) and its derivatives give only low yields.

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.