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Diastereoselective Diels–Alder Reaction on Carbohydrate Matrices

✍ Scribed by Prof. Dr. Horst Kunz; Dipl.-Chem. Bernd Müller; Dirk Schanzenbach


Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
356 KB
Volume
26
Category
Article
ISSN
0044-8249

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Diastereoselective Diels–Alder Reaction
✍ Daniele Passarella; Giordano Lesma; Marisa Martinelli; Alessandra Silvani; Marga 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 89 KB

AbstractÐ5-(Indol-2-yl)-pyran-2-one undergoes cycloaddition to electron-poor and electron-rich dienophiles. Lanthanide shift reagents have been shown to be ef®cient catalysts for the inverse electron demand Diels±Alder reactions. The bicycloadducts were formed with complete stereoselectivity. Aminol