Chemischer Informationsdienst
 1984
DOI: 10.1002/chin.198441104
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ChemInform Abstract: STEREOCHEMICAL ASPECTS OF 1,3‐DIPOLAR CYCLOADDITION OF BENZ(DE)ISOQUINOLINIUM‐1‐IDE AND NAPHTHO(1,8‐CD)THIOPYRAN

Masazumi Ikeda1,
Masakazu Tamura2,
Masafumi Yamagishi3
et al.

Abstract: Während das Naphthothiopyran (I) bei der Cycloaddition mit Maleinimiden (II) überwiegend exo‐Produkte (IV) liefert, werden bei dem Benzisochinoliniumylid (V) dabei ausschließlich endo‐Produkte (VII) gebil‐ 27 det.

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