Pd(0)-Catalyzed Conjugate Addition of Benzylzinc Chlorides to α,β-Enones in an Atmosphere of Carbon Monoxide: Preparation of 1,4-Diketones.

ChemInform Abstract: The Michael Additio

ChemInform Abstract: The Michael Addition of Indoles and Pyrrole to α-, β-Unsaturated Ketones and Double-Conjugate 1,4-Addition of Indoles to Symmetric Enones Promoted by Pulverization-Activation Method and Thia-Michael Addition Catalyzed by Wet Cyanuric Chloride.

✍ Ramin Ghorbani-Vaghei; Hojat Veisi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB

## Abstract The formation of cyanuric acid in wet cyanuric chloride catalyzes the solvent‐free addition of indole, pyrrole, and thiols to α,β‐unsaturated ketones.