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Synlett 2002(1): 0161-0163
DOI: 10.1055/s-2002-19361
DOI: 10.1055/s-2002-19361
LETTER
© Georg Thieme Verlag Stuttgart · New York
Vanadium-catalyzed Enantioselective Sulfoxidation of Methyl Aryl Sulfides with Hydrogen Peroxide as Terminal Oxidant
Further Information
Received
5 November 2001
Publication Date:
01 February 2007 (online)
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. -
1b
Kagan H. In Asymmetric Oxidation Reactions: Practical Approach in ChemistryKatsuki T. Oxford University Press; Oxford: 2001. Chap. 4.1. - 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] ).