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

作者信息

Ortiz-Marciales Margarita, De Jesús Melvin, González Eduvigis, Raptis Raphael G, Baran Peter

机构信息

Department of Chemistry, University of Puerto Rico, Humacao CUH Station, Humacao, PR 00791, USA.

出版信息

Acta Crystallogr C. 2004 Mar;60(Pt 3):o173-5. doi: 10.1107/S0108270104000666. Epub 2004 Feb 10.

Abstract

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.

摘要

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本文引用的文献

1
Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method.
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Coordinative N-->B bond formation and hydrogen-bonded molecular ladders in 2,5-bis[(N-->B)-(2-aminoethoxy)phenylboryl]thiophene.
Acta Crystallogr C. 2002 Aug;58(Pt 8):o515-7. doi: 10.1107/s0108270102010594. Epub 2002 Jul 31.
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