This review deals with the metal promoted asymmetric ring opening of achiral epoxides using achiral carbon-, nitrogen-, oxygen-, sulphur- and halogen-containing nucleophiles. The use of chiral bases in the asymmetric deprotonation of achiral epoxides yields chiral allylic alcohols. Finally, kinetic resolution of racemic epoxides can be achieved using chiral metal complexes.
机构:
Cent Drug Res Inst, Med & Proc Chem Div, Lucknow 226001, Uttar Pradesh, IndiaCent Drug Res Inst, Med & Proc Chem Div, Lucknow 226001, Uttar Pradesh, India
Mukherjee, Chinmoy
Maiti, Gour Hari
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Jadavpur Univ, Dept Chem, Kolkata 700032, IndiaCent Drug Res Inst, Med & Proc Chem Div, Lucknow 226001, Uttar Pradesh, India
Maiti, Gour Hari
Misra, Anup Kumar
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Cent Drug Res Inst, Med & Proc Chem Div, Lucknow 226001, Uttar Pradesh, IndiaCent Drug Res Inst, Med & Proc Chem Div, Lucknow 226001, Uttar Pradesh, India
机构:
Department of Biochemistry, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9038, United StatesDepartment of Biochemistry, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9038, United States
Pu, Xiaotao
Qi, Xiangbing
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Department of Biochemistry, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9038, United StatesDepartment of Biochemistry, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9038, United States
Qi, Xiangbing
Ready, Joseph M.
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Department of Biochemistry, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9038, United StatesDepartment of Biochemistry, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9038, United States
Ready, Joseph M.
Journal of the American Chemical Society,
2009,
131
(30):
: 10364
-
10365