Volume 27, Issue 16
Preparative Organic Chemistry
Full Access

ChemInform Abstract: Diastereoselective Reduction of α-(p-Tolylsulfinyl)ketoximes.

K. MIYASHITA

K. MIYASHITA

Fac. Pharm. Sci., Osaka Univ., Suita, Osaka 565, Japan

Search for more papers by this author
T. TOYODA

T. TOYODA

Fac. Pharm. Sci., Osaka Univ., Suita, Osaka 565, Japan

Search for more papers by this author
H. MIYABE

H. MIYABE

Fac. Pharm. Sci., Osaka Univ., Suita, Osaka 565, Japan

Search for more papers by this author
T. IMANISHI

T. IMANISHI

Fac. Pharm. Sci., Osaka Univ., Suita, Osaka 565, Japan

Search for more papers by this author
First published: April 16, 1996

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

Treatment of α-sulfinylketoximes according to A) results in the first reported diastereoselective reduction via a nonchelate model yielding (S)-(N-methoxyamino)sulfoxides. Further reductive fission of the C-S and N-O bonds of the products, e.g. (IIc) followed by acetylation leads to chiral amines (V), thus providing a suitable approach to this type of compounds.

chemical structure image

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