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Structurally Novel Bi- and Tricyclic β-Lactams via [2 + 2] Cycloaddition or Radical Reactions in 2-Azetidinone-Tethered Enallenes and Allenynes.

✍ Scribed by Benito Alcaide; Pedro Almendros; Cristina Aragoncillo


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

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✍ 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.