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

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Published inChemInform Vol. 35; no. 28; p. no
Main Authors Adam, Waldemar, Bosio, Sara G., Turro, Nicholas J., Wolff, Barbara T.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 13.07.2004
WILEY‐VCH Verlag
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Abstract For see ChemInform in Full Text.
AbstractList Abstract For Abstract see ChemInform Abstract in Full Text.
For see ChemInform in Full Text.
Author Wolff, Barbara T.
Turro, Nicholas J.
Adam, Waldemar
Bosio, Sara G.
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References Waldemar Adam, Sara G. Bosio, Nicholas J. Turro, Barbara T. Wolff, 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., J. Org. Chem., 2004, 69, 1704-1715.
2004; 69
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  article-title: 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.
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SubjectTerms dehydrogenation
diastereoselective syntheses
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
enantioselective syntheses (incl. cis/trans-isomerism)
oxazole derivatives
oxidation
oxidation, dehydrogenation
Title 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
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Volume 35
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