Abstract

tert-Butylphosphaacetylene (1) reacts at 120 °C with the bicyclic form of cis-7,8-dichlorocycloocta-1,3,5-triene (11) in a Diels-Alder reaction to furnish the tricyclic product 12, whose constitution was confirmed by single crystal structure analysis of the corresponding η 1-pentacarbonyltungsten complex 14. Compound 12 possess a sterically fixed 1,4-diene system and fulfills the structural prerequisite for homo-Diels-Alder reactions, which can be realized with the electron-poor acetylenes 15 as well as phosphaacetylene 1 (→ 16, 20). Furthermore, the polycyclic systems 16 can be oxidized and complexed at the phosphorus atom (→ 18, 19).

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