Volume 29, Issue 1
Preparative Organic Chemistry
Full Access

ChemInform Abstract: Double Asymmetric Dihydroxylation of 1,5-Hexadiene.

M. E. MAIER

M. E. MAIER

Fachbereich Chem., Martin-Luther-Univ. Halle-Wittenberg, D-06120 Halle/S., Germany

Search for more papers by this author
S. REUTER

S. REUTER

Fachbereich Chem., Martin-Luther-Univ. Halle-Wittenberg, D-06120 Halle/S., Germany

Search for more papers by this author
First published: 24 June 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 reaction gives in one-step a mixture of the tetrols (II) and (III) in a ratio of 3.4:1. From this ratio a facial selectivity of 6.65:1 for each double bond can be calculated. The compounds (II)/(III) serve as starting material for the preparation of the derivatives (VI) and (VII). While the separation of the diastereomers is not possible so far, this route for their preparation is useful because it is very short.

chemical structure image

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