PREPARATION DE DERIVES DIHYDRO-4,7 ISOINDOLIQUES ET ETUDE PRELIMINAIRE DE LEUR REACTIVITE A L'EGARD D'ALCENES ET D'ALCYNES ELECTROPHILES.

DOI: 10.1016/0040-4039(88)85325-5

Source and publish data:

Tetrahedron Letters p. 1025 - 1028 (1988)

Update date:2022-09-26

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Authors:

Stephan, Dominique

Gorgues, Alain

Le Coq, Andre

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Article abstract of DOI:10.1016/0040-4039(88)85325-5

The 4,7-dihydroisoindolic derivatives I are prepared through two pathways from acetylenedicarbaldehyde monoacetal.When reacted with electrophilic alkenes and alkynes under neutral conditions, they give rise to Diels-Alder and pseudo-Michael addition-subst

Full text of DOI:10.1016/0040-4039(88)85325-5

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Product name:[1-(3-Diethoxymethyl-bicyclo[2.2.2]octa-2,5-dien-2-yl)-meth-(E)-ylidene]-phenyl-amine

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