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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

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Abstract

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.

About this research paper

What this paper is about

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.

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Available abstract

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.

Key concepts: Chemistry, Michael reaction, Conjugate, Addition reaction, Pyrrole, Organic chemistry, Medicinal chemistry, Combinatorial chemistry

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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. — Research Paper | ScholarLens