Volume 21, Issue 37
Heterocyclic Compounds
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ChemInform Abstract: Enantioselective Intramolecular Diels-Alder Reactions of Trienes Synthesized from Monosaccharides.

P. HERCZEGH

P. HERCZEGH

Kossuth Lajos Tudomanyegyetem, MTA Antibiotikum-Kemiai Tanszek, 4010 Debrecen, Hungary

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M. ZSELY

M. ZSELY

Kossuth Lajos Tudomanyegyetem, MTA Antibiotikum-Kemiai Tanszek, 4010 Debrecen, Hungary

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G. BATTA

G. BATTA

Kossuth Lajos Tudomanyegyetem, MTA Antibiotikum-Kemiai Tanszek, 4010 Debrecen, Hungary

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Z. DINYA

Z. DINYA

Kossuth Lajos Tudomanyegyetem, MTA Antibiotikum-Kemiai Tanszek, 4010 Debrecen, Hungary

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R. BOGNAR

R. BOGNAR

Kossuth Lajos Tudomanyegyetem, MTA Antibiotikum-Kemiai Tanszek, 4010 Debrecen, Hungary

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L. SZILAGYI

L. SZILAGYI

Kossuth Lajos Tudomanyegyetem, MTA Antibiotikum-Kemiai Tanszek, 4010 Debrecen, Hungary

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I. BAJZA

I. BAJZA

Kossuth Lajos Tudomanyegyetem, MTA Antibiotikum-Kemiai Tanszek, 4010 Debrecen, Hungary

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First published: September 11, 1990

Abstract

Starting with the tribenzylated xylose (I), the nonatrienes (II) and (III) are synthesized.

ChemInform Abstract

Starting with the tribenzylated xylose (I), the nonatrienes (II) and (III) are synthesized. The glucose derivative (IV) is converted to the trienes (V) and (VI). The thermally induced intramolecular Diels-Alder cycloaddition of these trienes produces selectively the bicyclic olefins (VII) - (X).

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