Volume 19, Issue 2
Heterocyclic Compounds
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ChemInform Abstract: Trichloroethylidenarenesulfonamides in the Reactions with Furan and Its Derivatives.

G. G. LEVKOVSKAYA

G. G. LEVKOVSKAYA

Irkutskii inst. org. khim. Sib. otd. Akad. nauk SSSR

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I. T. EVSTAF'EVA

I. T. EVSTAF'EVA

Irkutskii inst. org. khim. Sib. otd. Akad. nauk SSSR

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A. N. MIRSKOVA

A. N. MIRSKOVA

Irkutskii inst. org. khim. Sib. otd. Akad. nauk SSSR

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S. N. ZHURAVLEV

S. N. ZHURAVLEV

Irkutskii inst. org. khim. Sib. otd. Akad. nauk SSSR

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V. G. KUL'NEVICH

V. G. KUL'NEVICH

Irkutskii inst. org. khim. Sib. otd. Akad. nauk SSSR

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First published: January 12, 1988

Abstract

The title compounds (III) are prepared from (I) and trichloroethene (II) by a well known one-step procedure.

ChemInform Abstract

The title compounds (III) are prepared from (I) and trichloroethene (II) by a well known one-step procedure. The title compounds (III) which are stable, are not isolated, but treated in situ with furan (IVa) or 2-methylfuran (IVb) to give the hitherto unknown compounds (V), which result from C-amidoalkylation reactions. The reactions between the title compound (IIIa) and 2-hydroxymethylfuran (VI)or furan-2-carboxylic acid (VIII) yield the novel compounds (VII) or (IX), which are the products of O-arenesulfonamido alkylation. The title compounds do not react with furans carrying electronegative substituents, as e.g. 2-acetylfuran or 2-ethoxyfuran.

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