A 1,3,2-oxazaborolidine dimer derived from (S)-α, α-diphenylprolinol

The reaction of (S)-alpha,alpha-diphenylprolinol with an excess of borane-tetrahydrofuran complex yields a stable crystalline material with the composition C34H38B2N2O2, which features a borane adduct of a spirocyclic structure with two oxazaborolidine rings joined by a central tetrahedral B atom. T...

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Veröffentlicht in:Acta crystallographica. Section C, Crystal structure communications Crystal structure communications, 2004-03, Vol.60 (Pt 3), p.o173-o175
Hauptverfasser: ORTIZ-MARCIALES, Margarita, DE JESUS, Melvin, GONZALEZ, Eduvigis, RAPTIS, Raphael G, BARAN, Peter
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Sprache:eng
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Zusammenfassung:The reaction of (S)-alpha,alpha-diphenylprolinol with an excess of borane-tetrahydrofuran complex yields a stable crystalline material with the composition C34H38B2N2O2, which features a borane adduct of a spirocyclic structure with two oxazaborolidine rings joined by a central tetrahedral B atom. This dimeric oxazaborolidine complex, viz. 3,3,3',3'-tetraphenyl-1,1'-spirobi(3a,4,5,6-tetrahydro-3H-pyrrolo[1,2-c][1,3,2]oxazaborole)-7-borane, is the dominant product under various reaction conditions; its crystal structure is consistent with 11B, 1H and 13C NMR and IR analyses.
ISSN:0108-2701
1600-5759
DOI:10.1107/S0108270104000666