Subscribe to RSS
DOI: 10.1055/s-2002-19361
Vanadium-catalyzed Enantioselective Sulfoxidation of Methyl Aryl Sulfides with Hydrogen Peroxide as Terminal Oxidant
Publication History
Publication Date:
01 February 2007 (online)

Abstract
Chiral vanadium complex prepared in situ from VO(acac)2 and Schiff base 9 was found to be an efficient catalyst for oxidation of various methyl aryl sulfides with hydrogen peroxide as terminal oxidant. For example, oxidation of methyl 2-naphthyl sulfide using a VO(acac)2, 9, and hydrogen peroxide system proceeded with high enantioselectivity of 93% ee as well as acceptable chemical yield.
Key words
asymmetric catalysis - chiral vanadium complex - Schiff base - enantioselective sulfoxidation - hydrogen peroxide
- 1a 
             
            Kagan H. In Catalytic Asymmetric SynthesisOjima I. Wiley-VCH; New York: 2000. Chap. 6c.Reference Ris Wihthout Link
- 1b 
             
            Kagan H. In Asymmetric Oxidation Reactions: Practical Approach in ChemistryKatsuki T. Oxford University Press; Oxford: 2001. Chap. 4.1.Reference Ris Wihthout Link
- 2 
             
            Pitchen P.Dunach E.Deshmukh MN.Kagan HB. J. Am. Chem. Soc. 1984, 106: 8188
- 3 
             
            Di Furia F.Modena G.Seraglia R. Synthesis 1984, 325
- 4 
             
            Brunel JM.Kagan HB. Synlett 1996, 404
- For other catalytic asymmetric sulfoxidations, see:
- 5a 
             
            Yamamoto K.Ando H.Shuetake T.Chikamatsu H. J. Chem. Soc., Chem. Commun. 1989, 754
- 5b 
             
            Komatsu N.Nishi-Bayashi Y.Sugita T.Uemura S. Tetrahedron Lett. 1992, 33: 5391
- 5c 
             
            Boche G.Möbus K.Harms K.Marsch M. J. Am. Chem. Soc. 1996, 118: 2770
- 5d 
             
            Liu G.Cogan DA.Ellman JA. J. Am. Chem. Soc. 1997, 119: 9913
- 5e 
             
            Yamanoi Y.Imamoto T. J. Org. Chem. 1997, 62: 8560
- 5f 
             
            Reetz MT.Merk C.Naberfeld G.Rudolph J.Griebenow N.Goddard R. Tetrahedron Lett. 1997, 38: 5273
- 5g 
             
            Peng Y.Feng X.Cui X.Jiang Y.Chan ASC. Synth. Commun. 2001, 31: 2287
- 5h 
             
            Skarzewski J.Ostrycharz E.Siedlecka R.Zielinska-Blajet M.Pisarski B. J. Chem. Res., Synop. 2001, 263
- 6a 
             
            Nakajima K.Kojima M.Fujita J. Chem. Lett. 1986, 1483
- 6b 
             
            Nakajima K.Kojima K.Kojima M.Fujita J. Bull. Chem. Soc. Jpn. 1990, 63: 2620
- 7 
             
            Palucki M.Hanson P.Jacobsen EN. Tetrahedron Lett. 1992, 33: 7111
- 8a 
             
            Noda K.Hosoya N.Irie R.Yamashita Y.Katsuki T. Tetrahedron 1994, 50: 9609
- 8b 
             
            Kokubo C.Katsuki T. Tetrahedron 1996, 52: 13895
- 9 
             
            Saito B.Katsuki T. Tetrahedron Lett. 2001, 42: 3873
- 10a 
             
            Bolm C.Bienewald F. Angew. Chem., Int. Ed. Engl. 1995, 34: 2640
- 10b 
             
            Bolm C.Bienewald F. Synlett 1998, 1327
- 11 
             
            Vetter AH.Berkessel A. Tetrahedron Lett. 1998, 39: 1741
- 12a 
             
            Katsuki T. J. Mol. Cat. A: Chem. 1996, 113: 87
- 12b 
             
            Ito YN.Katsuki T. Bull. Chem. Soc. Jpn. 1999, 72: 603
- 14 
             
            Nishikori H.Katsuki T. Tetrahedron Lett. 1996, 37: 9245
- 15 
             
            Saito S.Kano T.Muto H.Nakadai M.Yamamoto H. J. Am. Chem. Soc. 1999, 121: 8943
- 16a 
             
            Karpyshev NN.Yakovleva OD.Talsi EP.Bryliakov KP.Tolstikova OV.Tolstikov AG. J. Mol. Cat. A: Chem. 2000, 157: 91
- 16b 
             
            Bryliakov KP.Karpyshev NN.Forminsky SA.Tolstikov AG.Talsi EP. J. Mol. Cat. A: Chem. 2001, 171: 73
- 17 
             
            Sakuraba H.Natori K.Tanaka Y. J. Org. Chem. 1991, 56: 4124
References
Although we synthesized compound 8 according to the reported procedure (ref. [14] ), it can be prepared enantioselectively in a short step by using Yamamoto procedure (ref. [15] ).
 
    