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ChemInform Abstract: A Remarkable Stereocontrol During Cobalt(II) Chloride Catalyzed Opening of Cinnamoyl Epoxides with N-Substituted Anilines. by A. DE; S. GHOSH; J. IQBAL is a Chemistry article available to read on EtoBox.
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A Remarkable Stereocontrol During Cobalt(II) Chloride Catalyzed Opening of Cinnamoyl Epoxides with N-Substituted Anilines. -The stereochemistry of the ring cleavage is controlled by the para-substituent of the aromatic ring directly attached to the nitrogen of the aniline. para-Methoxy groups cause formation of anti amino alcohols; amines with para-Cl, -Br, -Me, or hydrogen substituents afford syn products. -(DE, A.
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- Author
- A. DE; S. GHOSH; J. IQBAL
- Publisher
- John Wiley and Sons; Wiley (John Wiley & Sons); Wiley (ISSN 0931-7597)
- Published
- 1998
- Language
- EN
- Field
- Chemistry (Physical Sciences)