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
Hauptverfasser: Kajiyama, Kazumasa, Fujimori, Sayaka, Yasuoka, Daisuke, Otsuka, Takeshi, Miyamoto, Takeshi
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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.
ISSN:0040-4020
DOI:10.1016/j.tet.2013.08.004