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ChemInform Abstract: On-Water Vinylogous Mukaiyama—Michael Addition of Heterocyclic 2-Silyloxydienes to 1,2-Diaza-1,3-dienes: One-Pot Three-Step Entry to Functionality-Rich Pyrroles.

✍ Scribed by Lucia Battistini; Luca Dell'Amico; Andrea Sartori; Claudio Curti; Giorgio Pelosi; Giovanni Casirgahi; Orazio A. Attanasi; Gianfranco Favi; Franca Zanardi

Publisher: John Wiley and Sons
Year: 2011
Weight: 35 KB
Volume: 43
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201203092

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✍ Lucia Battistini; Luca Dell'Amico; Andrea Sartori; Claudio Curti; Giorgio Pelosi 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 378 KB

## Abstract Densely substituted pyrrole‐carboxylates have been prepared in good yields in a highly practical one‐pot three‐step procedure. The key reaction of this process, which involves an uninterrupted sequence of reactions on‐water, is a diastereoselective vinylogous Mukaiyama–Michael addition

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