Volume 21, Issue 21
Isocyclic Compounds
Full Access

ChemInform Abstract: The Configuration of trans-5-Nitro-6-glyconorbornenes. Synthesis of the Enantiomerically Pure trans-5-Nitronorbornene-6-carboxaldehydes.

J. A. SERRANO

J. A. SERRANO

Dep. Quim. Org., Fac. Cienc., Univ. Extremadura, 06071 Badajoz, Spain

Search for more papers by this author
E. ROMAN

E. ROMAN

Dep. Quim. Org., Fac. Cienc., Univ. Extremadura, 06071 Badajoz, Spain

Search for more papers by this author
First published: May 22, 1990

Abstract

The diastereomeric mixture of the glyconorbornenes (I) is deacetylated and the isomers are isolated by fractional crystallization.

ChemInform Abstract

The diastereomeric mixture of the glyconorbornenes (I) is deacetylated and the isomers are isolated by fractional crystallization. These are oxidatively cleaved to produce the diastereomerically pure nitro aldehydes (II) - (V). Their structures are established by 1H and 13C NMR spectroscopy.

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