Synthesis of axially chiral N-hydroxyimides, potential new catalysts for asymmetric oxidations

Journal of Organic Chemistry

Volumn 64, Issue 12, 1999, Pages 4542-4546

  Einhorn, Cathy ^a   Einhorn, Jacques ^a   Marcadal Abbadi, Céline ^a   Pierre, Jean Louis ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

2 HYDROXY 4 (2 PHENYLPHENYL)BENZO[F]ISOINDOLE 1,3 DIONE; IMIDE; N HYDROXYIMIDE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; OPTICAL ROTATION; OXIDATION; REACTION ANALYSIS; STRUCTURE ACTIVITY RELATION; SYNTHESIS;

EID: 0033546254     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo982527o     Document Type: Article

References (36)

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24. -1.
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26. 3) to a dilute solution of ketone 8b. Splitting of the OMe singlet was observed for racemic 8b.
27. Enantiomeric composition has been determined by GLC on a Chiraldex B-PM capillary column, with an oven temperature of 130 °C.
28. -1.
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32. 1H NMR of the crude mixture.
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