Abstract
A series of hydrazonyl chlorides bearing an alkenyl chain have been synthesised and treated with silver carbonate. The propensity of the so-formed nitrite Imine intermediates to undergo intramolecular cycloaddition is markedly dependent on the length and the flexibility of the chain. The latter also affected the regio- and the stereo-chemistry of the Intramolecular process. In certain circumstances, tandem intermolecular–Intramolecular cycloadditions took place, to produce largering heterophanes.
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