Melting point	29-33 ºC

SDS/MSDS	S24/25

Source	SDS/MSDS Samples
Alfa-Aesar	View & Download
Sigma-Aldrich	View & Download
TCI	View & Download

Synthetic Route

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Articles

Peer-Reviewed Papers

Noyori, R. et al. Journal of the American Chemical Society, 106(22), 6709-6709 (1984) Molecular design of a chiral Lewis acid for the asymmetric Claisen rearrangement.Maruoka, K. et al. Journal of the American Chemical Society, 117(3), 1165-1165 (1995) Catalytic asymmetric oxidation of sulfides to sulfoxides with tert-butyl hydroperoxide using binaphthol as a chiral auxiliary.Komatsu N, et al. The Journal of Organic Chemistry, 58, 4529-4529 (1993) New chiral binaphthalene-derived iminium salt organocatalysts for asymmetric epoxidation of alkenes.Philip C Bulman Page et al.The Journal of organic chemistry, 72(12), 4424-4430 (2007-05-18) Evaluation of co-solvent fraction, pressure and temperature effects in analytical and preparative supercritical fluid chromatography.Dennis Åsberg et al.Journal of chromatography. A, 1374, 254-260 (2014-12-17) Catalytic asymmetric epoxidation with (Salen) manganese (III) complex bearing binaphthyl groups of axial chirality.Sasaki, H. et al. Synlett, 1993(04), 300-300 (1993) Asymmetric aza-Diels-Alder reaction catalyzed by boron reagent: Effect of biphenol and binaphthol ligand.Hattori, K. Yamamoto, H. Synlett, 1993(02), 129-129 (1993) Asymmetric Diels-Alder reactions catalyzed by chiral lanthanide (III) trifluoromethanesulfonates. Unique structure of the triflate and stereoselective synthesis of both enantiomers using a single chiral source and a choice of achiral ligands.S. Kobayashi et al. Tetrahedron, 50(40), 11623-11623 (1994)

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