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Highly Enantio- and Diastereoselective Organocatalytic Asymmetric Domino Michael–Aldol Reaction of β-Ketoesters and α,β-Unsaturated Ketones

✍ Scribed by Nis Halland; Pompiliu S. Aburel; Karl Anker Jørgensen

Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
164 KB
Volume
43
Category
Article
ISSN
0044-8249

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Highly Enantio- and Diastereoselective O
Highly Enantio- and Diastereoselective Organocatalytic Domino Michael-Aldol Reactions of β-Diketone and β-Ketosulfone Nucleophiles with α,β-Unsaturated Ketones
✍ Juha Pulkkinen; Pompiliu S. Aburel; Nis Halland; Karl Anker Jørgensen 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 97 KB 👁 2 views

## Abstract A chiral imidazolidine catalyst was shown to catalyze the highly enantio‐ and diastereoselective domino Michael‐aldol reaction of β‐diketone and β‐ketosulfone derivatives with α,β‐unsaturated ketones to form optically active cyclohexanones having three or four contiguous chiral centers.