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Expeditious Entry to Enantiopure Mono- and Bis(Tricyclic) β-Lactams by Single or Double [2+2] Cycloaddition of Allenynes

✍ Scribed by Benito Alcaide; Pedro Almendros; Cristina Aragoncillo; Gonzalo Gómez-Campillos

Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
733 KB
Volume
2011
Category
Article
ISSN
1434-193X

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ChemInform Abstract: Expeditious Entry t
ChemInform Abstract: Expeditious Entry to Enantiopure Mono- and Bis(tricyclic) β-Lactams by Single or Double [2 + 2] Cycloaddition of Allenynes.
✍ Benito Alcaide; Pedro Almendros; Cristina Aragoncillo; Gonzalo Gomez-Campillos 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 61 KB 👁 1 views

## Abstract Thermal cycloaddition of β‐lactam‐tethered allenynes, e.g. (III), provides access to structurally novel tricyclic β‐lactams containing a seven‐membered ring and a strained cyclobutene ring.