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ChemInform Abstract: An Efficient Synthesis of Highly Functionalized 4-Substituted 2-Azetidinones by a Stereoselective Intermolecular Diels—Alder Reaction of Different Types of 2-Azetidinone-Tethered Dienes.

✍ Scribed by Benito Alcaide; Pedro Almendros; Nati R. Salgado; Mari Paz Martinez-Alcazar; Felix Hernandez-Cano


Publisher
John Wiley and Sons
Year
2010
Weight
37 KB
Volume
33
Category
Article
ISSN
0931-7597

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An Efficient Synthesis of Highly Functio
✍ Benito Alcaide; Pedro Almendros; Nati R. Salgado; Mari Paz Martínez-Alcázar; Fél 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 453 KB 👁 2 views

The diastereoselectivity of the intermolecular Diels-Alder reaction of 2-azetidinone-tethered dienes was investigated. Diene precursors were prepared from 4-azetidinone-2-carbaldehydes through an allylation-dehydration process or by the sequence Wittig reaction/enolate trapping. Dienes with a βlacta