熔点	76 ºC**
密度	0.886±0.06 g/cm3 (20 º

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Dibutylboron triflate promoted conjugate addition of benzylic and allylic organocopper reagents to chiral α,β-unsaturated N-acyl imidazolidinones.van Heerden PS, et al. Tetrahedron Letters, 37(39), 6985-6988 (1996) Synlett, 81-81 (1992) Palladium-catalyzed oxidative cyclizations: synthesis of dihydropyranones and furanones.Maud Reiter et al.The Journal of organic chemistry, 70(21), 8478-8485 (2005-10-08) Stereo-and regio-controlled aldol synthesis. Kuwajima I, et al. Tetrahedron Letters, 21(44), 4291-4294 (1980) Stereoselective aldol-type cyclization reaction mediated by dibutylboron triflate/diisopropylethylamine.Sanjib Das et al.Organic letters, 6(1), 123-126 (2004-01-03) Journal of the American Chemical Society, 115, 2613-2613 (1993) Efficient one-step aldol-type reaction of ketones with acetals and ketals mediated by dibutylboron triflate/diisopropylethyl amine.Lian-Sheng Li et al.Organic letters, 6(1), 127-130 (2004-01-03) Boron-complexation strategy for use with 1-acyldipyrromethanes.Kannan Muthukumaran et al.The Journal of organic chemistry, 69(16), 5354-5364 (2004-08-04) Tandem Wittig rearrangement/aldol reactions for the synthesis of glycolate aldols.Myra Beaudoin Bertrand et al.Organic letters, 8(20), 4661-4663 (2006-09-22)

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