A remarkable stereocontrol during cobalt(II) chloride catalysed opening of cinnamoyl epoxides with N-substituted anilines

ChemInform Abstract: A Remarkable Stereo

ChemInform Abstract: A Remarkable Stereocontrol During Cobalt(II) Chloride Catalyzed Opening of Cinnamoyl Epoxides with N-Substituted Anilines.

✍ A. DE; S. GHOSH; J. IQBAL 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

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