Enecarbamates as selective substrates in oxidations: chiral-auxiliary-controlled mode selectivity and diastereoselectivity in the [2+2] cycloaddition and ene reaction of singlet oxygen and in the epoxidation by DMD and mCPBA.
about
The outcome of the oxidations of unusual enediamide motifs is governed by the stabilities of the intermediate iminium ionsNew singlet oxygen donors based on naphthalenes: synthesis, physical chemical data, and improved stability.Supramolecular photochirogenesis.Studies in organic and physical photochemistry - an interdisciplinary approach.Computational study of the mechanism and selectivity of ruthenium-catalyzed hydroamidations of terminal alkynesmeta-Chloroperbenzoic acid (mCPBA): a versatile reagent in organic synthesis
P2860
Enecarbamates as selective substrates in oxidations: chiral-auxiliary-controlled mode selectivity and diastereoselectivity in the [2+2] cycloaddition and ene reaction of singlet oxygen and in the epoxidation by DMD and mCPBA.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年學術文章
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name
Enecarbamates as selective sub ...... epoxidation by DMD and mCPBA.
@en
Enecarbamates as selective sub ...... epoxidation by DMD and mCPBA.
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type
label
Enecarbamates as selective sub ...... epoxidation by DMD and mCPBA.
@en
Enecarbamates as selective sub ...... epoxidation by DMD and mCPBA.
@nl
prefLabel
Enecarbamates as selective sub ...... epoxidation by DMD and mCPBA.
@en
Enecarbamates as selective sub ...... epoxidation by DMD and mCPBA.
@nl
P2093
P356
P1476
Enecarbamates as selective sub ...... epoxidation by DMD and mCPBA.
@en
P2093
Barbara T Wolff
Nicholas J Turro
Sara G Bosio
P304
P356
10.1021/JO035745C
P407
P577
2004-03-01T00:00:00Z