Reactions of 1-ethyl-1,2-diphosphole with acetylenes

The cycloaddition of 1-ethyl-3,4,5-triphenyl-1,2-diphosphacyclopenta-2,4-diene to acetylenes R 1 C≡CR 2 (R 1 = R 2 = CO 2 Me; R 1 = Ph, R 2 = H) gives phosphinine along with oligomeric products. In the case of nonsymmetric phenylacetylene, the process is regioselective.

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Veröffentlicht in:Russian chemical bulletin 2015-08, Vol.64 (8), p.1986-1988
Hauptverfasser: Zagidullin, A. A., Ganushevich, Yu. S., Kafiyatullina, A. G., Miluykov, V. A., Sinyashin, O. G.
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Sprache:eng
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Zusammenfassung:The cycloaddition of 1-ethyl-3,4,5-triphenyl-1,2-diphosphacyclopenta-2,4-diene to acetylenes R 1 C≡CR 2 (R 1 = R 2 = CO 2 Me; R 1 = Ph, R 2 = H) gives phosphinine along with oligomeric products. In the case of nonsymmetric phenylacetylene, the process is regioselective.
ISSN:1066-5285
1573-9171
DOI:10.1007/s11172-015-1106-0