Asymmetric synthesis of densely functionalized 3-substituted 3-hydroxy-β-lactams via novel, highly stereoselective Baylis-Hillman and allylation reactions of enantiopure 3-oxo-2-azetidinones
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作者:
Alcaide, B
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Univ Complutense, Fac Ciencias Quim, Dept Quim Organ 1, E-28040 Madrid, SpainUniv Complutense, Fac Ciencias Quim, Dept Quim Organ 1, E-28040 Madrid, Spain
Alcaide, B
[1
]
Almendros, P
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Univ Complutense, Fac Ciencias Quim, Dept Quim Organ 1, E-28040 Madrid, SpainUniv Complutense, Fac Ciencias Quim, Dept Quim Organ 1, E-28040 Madrid, Spain
Almendros, P
[1
]
Aragoncillo, C
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Univ Complutense, Fac Ciencias Quim, Dept Quim Organ 1, E-28040 Madrid, SpainUniv Complutense, Fac Ciencias Quim, Dept Quim Organ 1, E-28040 Madrid, Spain
Aragoncillo, C
[1
]
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[1] Univ Complutense, Fac Ciencias Quim, Dept Quim Organ 1, E-28040 Madrid, Spain
New asymmetric routes based on both Baylis-Hillman and allylation reactions of enantiopure 3-oxo-2-azetidinones are used for the highly stereoselective, efficient preparation of densely functionalized 3-substituted 3-hydroxy-beta-lactams. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.