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ChemInform Abstract: Enantioselective Trifunctional Organocatalysts for Rate-Enhanced Aza-Morita—Baylis—Hillman Reactions at Room Temperature.

✍ Scribed by Jean-Marc Garnier; Christopher Anstiss; Fei Liu

Publisher
John Wiley and Sons
Year
2009
Weight
25 KB
Volume
40
Category
Article
ISSN
0931-7597

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Enantioselective Trifunctional Organocat
Enantioselective Trifunctional Organocatalysts for Rate- Enhanced Aza-Morita–Baylis–Hillman Reactions at Room Temperature
✍ Jean-Marc Garnier; Christopher Anstiss; Fei Liu 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 364 KB 👁 1 views

## Abstract magnified image A Brønsted acid‐activated trifunctional organocatalyst, based on the BINAP scaffold, was used for the first time to catalyze aza‐Morita‐Baylis–Hillman reactions between __N__‐tosylimines and methyl vinyl ketone with fast reaction rates and good enantioselectivity at roo