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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 Joergensen

Publisher
John Wiley and Sons
Year
2004
Weight
183 KB
Volume
35
Category
Article
ISSN
0931-7597

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✦ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

📜 SIMILAR VOLUMES

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.

ChemInform Abstract: Organocatalytic Asy
ChemInform Abstract: Organocatalytic Asymmetric β-Hydroxylation of α,β-Unsaturated Ketones.
✍ Armando Carlone; Giuseppe Bartoli; Marcella Bosco; Fabio Pesciaioli; Paolo Ricci 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 43 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v