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 in | ChemInform Vol. 35; no. 28; p. no |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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Weinheim
WILEY-VCH Verlag
13.07.2004
WILEY‐VCH Verlag |
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Abstract | For see ChemInform in Full Text. |
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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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Cites_doi | 10.1021/jo035745c |
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Copyright | Copyright © 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim |
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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 e_1_2_2_1_2 |
References_xml | – volume: 69 start-page: 1704 year: 2004 end-page: 1715 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. publication-title: J. Org. Chem. – ident: e_1_2_2_1_2 doi: 10.1021/jo035745c |
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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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