Subscribe to RSS
DOI: 10.1055/s-2003-39321
Nb(salen)-Catalyzed Sulfoxidation
Publication History
Publication Date:
20 May 2003 (online)
Abstract
Niobium(salen) complex was found to be an effective catalyst for asymmetric oxidation of various sulfides using urea˙hydrogen peroxide as terminal oxidant.
Key words
niobium - asymmetric catalysis - sulfoxidation - niobium(salen) complex
-
1a
Catalytic Asymmetric Synthesis
2nd
ed.:
Ojima I. Wiley-VCH; New York: 2000. -
1b
Comprehensive Asymmetric
Catalysis
Jacobsen EN.Pfaltz A.Yamamoto H. Springer; Berlin: 2000. -
2a
Matsuda Y.Sakamoto S.Koshima H.Murakami Y. J. Am. Chem. Soc. 1985, 107: 6415 -
2b
Ushikubo T. Cat. Today 2000, 57: 331 -
Chen H.Dai W.-L.Jiang A.-R.Deng J.-F. Chem. Lett. 2002, 220 -
2c
Choi S.Yang J.-D.Ji M.Choi H.Kee M.Ahn K.-H.Byeon S.-H.Baik W.Koo S. J. Org. Chem. 2001, 66: 8192 -
2d
Kapoor MP.Raj A. Studies in Surface Science and Catalysis 2000, 129: 327 -
2e
Passoni LC.Siddiqui MRH.Steiner A.Kozhevnikov IV. J. Mol. Cat. A: Chem. 2000, 153: 103 - 3
Howarth J.Gillespie K. Molecules 2000, 5: 993 ; http://www.mdpi.org/molecules/papers/50800993.pdf - 4
Colletti SL.Halterman RL. J. Orgmet. Chem. 1993, 455: 99 - For the recent reviews on asymmetric sulfoxidation, see:
-
6a
Bolm C.Muniz K.Hildebrand JP. In Comprehen-sive Asymmetric Catalysis Vol. II:Jacobsen EN.Pfaltz A.Yamamoto H. Springer; Berlin: 1999. Chap. 19. -
6b
Kagan HB. In Catalytic Asymmetric Synthesis 2nd ed.:Ojima I. Wiley-VCH; New York: 2000. Chap. 6C. - 7
Katsuki T. Synlett 2003, 281 -
8a
Puchot C.Samuel O.Dunach E.Zhao S.Agami C.Kagan HB. J. Am. Chem. Soc. 1986, 108: 2353 -
8b
Kagan HB. Adv. Synth. Cat. 2001, 343: 227 - For examples of positive non-linear effect, see:
-
9a
Oguni N.Matsuda Y.Kaneko T. J. Am. Chem. Soc. 1988, 110: 7877 -
9b
Kitamura M.Okada S.Suga S.Noyori R. J. Am. Chem. Soc. 1989, 111: 4028 -
9c
Mikami K.Terada M.Nakai T. J. Am. Chem. Soc. 1990, 112: 3949 -
9d
Soai K.Niwa S.Hori H. J. Chem. Soc., Chem. Commun. 1990, 982 -
9e
Soai K.Shibata T. In Catalytic Asymmetric SynthesisOjima I. Wiley-VCH; New York: 2000. p.699 -
9f
Furuno H.Hanamoto T.Sugimoto Y.Inanaga J. Org.Lett. 2000, 2: 49 - 10 For the example of non-linear effect
in metallosalen-catalyzed oxidation, see:
Saito B.Katsuki T. Tetrahedron Lett. 2001, 42: 8333
References
Metallosalen complexes are usually prepared by mixing the corresponding metal ion (usually in the form of metal halide or metal alkoxide) and salen ligand under basic conditions or by mixing metal ion and a salen ligand pretreated with NaH. However, the niobium complex prepared from NbCl3(dme) and salen ligand in these ways showed inferior catalytic activity in terms of enantioselectivity (for examples, the oxidation of methyl phenyl sulfides with these Nb-4 complexes at room temperature showed 12-46% ee).
11Typical experiment procedure is exemplified with asymmetric oxidation of methyl phenyl sulfide with 4 as the chiral ligand: ligand 4 (10 mg, 12 µmol) and NbCl3(dme) (2.3 mg, 8.0 µmol) were dissolved in dichloromethane (2 mL) in a glovebox, and the solution was stirred for 2 h at room temperature. After addition of MS 4 Å (ca. 20 mg), the mixture was stirred for another 30 min. The mixture was taken out of the glovebox and cooled to -10 °C under nitrogen. To this mixture were added methyl phenyl sulfide (12.0 µL, 0.10 mmol) and urea˙hydrogen peroxide adduct (UHP) (10.5 mg, 0.11 mmol) successively, and the mixture was stirred for 2 days at the temperature. The mixture was directly chromatographed on silica gel (hexane-ethyl acetate = 1:1-1:19) to give methyl phenyl sulfoxide (12.4 mg, 88%). The enantiomeric excess of the sulfoxide was determined to be 86% ee by HPLC analysis using chiral stationary phase column (Daicel Chiralcel OD-H, hexane-i-PrOH = 9:1).