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Chiral Lewis Acid Catalyzed Asymmetric Baylis—Hillman Reactions.

✍ Scribed by Kung-Shuo Yang; Wei-Der Lee; Jia-Fu Pan; Kwunmin Chen


Publisher
John Wiley and Sons
Year
2003
Weight
21 KB
Volume
34
Category
Article
ISSN
0931-7597

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✦ Synopsis


Abstract

For Abstract see ChemInform Abstract in Full Text.


📜 SIMILAR VOLUMES


The Chiral Diamine Mediated Asymmetric B
✍ Yujiro Hayashi; Tomohiro Tamura; Mitsuru Shoji 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 117 KB 👁 2 views

## Abstract A chiral diamine, easily prepared from proline, is an effective, asymmetric organic catalyst for the Baylis–Hillman reaction of aldehydes and methyl vinyl ketone, affording adducts with enantioselectivities up to 75%.