SPOTLIGHT
© Georg Thieme Verlag Stuttgart · New York Chiral Ketone Catalysts Derived from d -Fructose H.-Q. Ge C/O Prof. Q.-H. Xia, Laboratory for Advanced Materials and New Catalysis, School of Chemistry and Material Science, Hubei University, Wuhan 430062, P. R. China Fax: +86(27)50865370; e-Mail: gehq2003@yahoo.com ;
References
<A NAME="RV09103ST-1">1 </A>
Tu Y.
Wang Z.-X.
Shi Y.
J. Am. Chem. Soc.
1996,
118:
9806
For leading references on asymmetric epoxidation catalyzed by chiral ketones see:
<A NAME="RV09103ST-2A">2a </A>
Curci R.
Fiorentino M.
Serio MR.
Chem. Commun.
1984,
155
<A NAME="RV09103ST-2B">2b </A>
Yang D.
Yip YC.
Tang MW.
Wong MK.
Zheng JH.
Cheung KK.
J. Am. Chem. Soc.
1996,
118:
491
<A NAME="RV09103ST-2C">2c </A>
Song CE.
Kim YH.
Lee KC.
Lee SG.
Jin BW.
Tetrahedron: Asymmetry
1997,
8:
2921
<A NAME="RV09103ST-2D">2d </A>
Armstrong A.
Hayter BR.
Chem. Commun.
1998,
621
<A NAME="RV09103ST-2E">2e </A>
Denmark SE.
Wu Z.
Synlett
1999,
847
<A NAME="RV09103ST-2F">2f </A>
Frohn M.
Shi Y.
Synthesis
2000,
1979
<A NAME="RV09103ST-2G">2g </A>
Wang Z.-X.
Miller SM.
Anderson OP.
Shi Y.
J. Org. Chem.
2001,
66:
521
<A NAME="RV09103ST-2H">2h </A>
Matsumoto K.
Tomioka K.
Tetrahedron Lett.
2002,
43:
631
<A NAME="RV09103ST-2I">2i </A>
Denmark SE.
Matsuhashi H.
J. Org. Chem.
2002,
67:
3479
<A NAME="RV09103ST-2J">2j </A>
Shing TKM.
Leung GYC.
Tetrahedron
2002,
58:
7545
<A NAME="RV09103ST-2K">2k </A>
Shu L.-H.
Wang P.-Z.
Gan Y.-H.
Shi Y.
Org. Lett.
2003,
5:
293
<A NAME="RV09103ST-3A">3a </A>
Wang Z.-X.
Tu Y.
Frohn M.
Zhang J.-R.
Shi Y.
J. Am. Chem. Soc.
1997,
119:
11224
<A NAME="RV09103ST-3B">3b </A>
Tian H.-Q.
She X.-G.
Shu L.-H.
Yu H.-W.
Shi Y.
J. Am. Chem. Soc.
2000,
122:
11551
<A NAME="RV09103ST-3C">3c </A>
Tian H.-Q.
She X.-G.
Yu H.-W.
Shu L.-H.
Shi Y.
J. Org. Chem.
2002,
67:
2435
<A NAME="RV09103ST-4">4 </A>
Yu X.-Y.
She X.-G.
Shi Y.
J. Am. Chem. Soc.
2002,
124:
8792
<A NAME="RV09103ST-5">5 </A>
Tian H.-Q.
She X.-G.
Shi Y.
Org. Lett.
2001,
3:
715
<A NAME="RV09103ST-6">6 </A>
Shu L.-H.
Shen Y.-M.
Burke C.
Goeddel D.
Shi Y.
J. Org. Chem.
2003,
68:
4963
<A NAME="RV09103ST-7">7 </A>
Wang Z.-X.
Tu Y.
Frohn M.
Shi Y.
J. Org. Chem.
1997,
62:
2328
<A NAME="RV09103ST-8A">8a </A>
Shu L.-H.
Shi Y.
Tetrahedron Lett.
1999,
40:
8721
<A NAME="RV09103ST-8B">8b </A>
Shu L.-H.
Shi Y.
Tetrahedron
2001,
57:
5213
<A NAME="RV09103ST-9">9 </A> Yoxone or YH2O2 stands for the yield when Oxone or H2 O2 is used as the oxidant; while Y1 ,Y3 or Y4 stands for the yield when ketone 1 , 3 or 4 is used as the catalyst
<A NAME="RV09103ST-10">10 </A>
Wang Z.-X.
Shi Y.
J. Org. Chem.
1998,
63:
3099
<A NAME="RV09103ST-11">11 </A>
Frohn M.
Dalkiewicz M.
Tu Y.
Wang Z.-X.
Shi Y.
J. Org. Chem.
1998,
63:
2948
<A NAME="RV09103ST-12A">12a </A>
Cao G.-A.
Wang Z.-X.
Tu Y.
Shi Y.
Tetrahedron Lett.
1998,
39:
4425
<A NAME="RV09103ST-12B">12b </A>
Wang Z.-X.
Cao G.-A.
Shi Y.
J. Org. Chem.
1999,
64:
7646
<A NAME="RV09103ST-13A">13a </A>
Zhu Y.-M.
Tu Y.
Yu H.-W.
Shi Y.
Tetrahedron Lett.
1998,
39:
7819
<A NAME="RV09103ST-13B">13b </A>
Zhu Y.-M.
Shu L.-H.
Tu Y.
Shi Y.
J. Org. Chem.
2001,
66:
1818
<A NAME="RV09103ST-14">14 </A>
Warren JD.
Shi Y.
J. Org. Chem.
1999,
64:
7675
<A NAME="RV09103ST-15">15 </A>
Frohn M.
Zhou X.-M.
Zhang J.-R.
Tang Y.
Shi Y.
J. Am. Chem. Soc.
1999,
121:
7718
<A NAME="RV09103ST-16">16 </A>
Tian H.-Q.
She X.-G.
Xu J.-X.
Shi Y.
Org. Lett.
2001,
3:
1929