Aroylspirophosphoranes bearing two naphth-1,8-diyl-8-oxy groups: synthesis, crystal structure, and np(Oapical)aIa(CO) charge transfer interaction
The reactions of aroyl chlorides with the lithium phosphoranide generated from bis(naphth-1,8-diyl-8-oxy)phosphorane 1 afforded aroylspirophosphoranes 3aaf. The p-anisoyl- and p-tert-butylbenzoylphosphoranes 3a and 3b bearing an electron-donating aryl group were stable to moisture on silica gel. The...
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Veröffentlicht in: | Tetrahedron 2013-10, Vol.69 (43), p.9155-9160 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The reactions of aroyl chlorides with the lithium phosphoranide generated from bis(naphth-1,8-diyl-8-oxy)phosphorane 1 afforded aroylspirophosphoranes 3aaf. The p-anisoyl- and p-tert-butylbenzoylphosphoranes 3a and 3b bearing an electron-donating aryl group were stable to moisture on silica gel. The crystal structures of p-anisoyl-, p-tert-butylbenzoyl-, benzoyl-, and p-fluorobenzoylphosphorane (3a, 3b, 3d, and 3e) elucidated by X-ray structural analysis suggested effective intramolecular np(Oapical)aIa(CO) charge transfer stabilization to be operative. |
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ISSN: | 0040-4020 |
DOI: | 10.1016/j.tet.2013.08.004 |