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A novel synthesis of tricyclic-fused hydrindene–azetidinone compounds by sequential Mn(III)-promoted 4-exo-trig cyclization/radical aromatic substitution

✍ Scribed by Alessandra Cerreti; Andrea D'Annibale; Corrado Trogolo *; Floriana Umani

Book ID: 104210194
Publisher: Elsevier Science
Year: 2000
Tongue: French
Weight: 116 KB
Volume: 41
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)00364-6

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✦ Synopsis

The 2-acyl-N-(2,2-diphenyl-1-ethenyl)-N-alkylacetamides reacted with excess Mn(III) affording tricyclic fused hydrindene-azetidinones in good yields, through a 4-exo-trig radical cyclization process, and further ring closure of the azetidinone via radical aromatic substitution.

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ChemInform Abstract: A Novel Synthesis o

ChemInform Abstract: A Novel Synthesis of Tricyclic-Fused Hydrindene—Azetidinone Compounds by Sequential Mn(III)-Promoted 4-exo-trig Cyclization/Radical Aromatic Substitution.

✍ Alessandra Cerreti; Andrea D'Annibale; Corrado Trogolo; Floriana Umani 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

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