## Abstract A simple and highly efficient method for the preparation of fully substituted pyrroles, from readily accessible secondary propargylic alcohols, 1,3βdicarbonyl compounds and primary amines, has been developed. The oneβpot multicomponent reaction, which is catalysed by the system [Ru(Ξ·^3^
ChemInform Abstract: One-Pot Three-Component Catalytic Synthesis of Fully Substituted Pyrroles from Readily Available Propargylic Alcohols, 1,3-Dicarbonyl Compounds and Primary Amines.
β Scribed by Victorio Cadierno; Jose Gimeno; Noel Nebra
- Publisher
- John Wiley and Sons
- Year
- 2008
- Weight
- 57 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0931-7597
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## Abstract magnified image Several tetrasubstituted Nο£ΏH pyrroles, functionalized with ester or ketone groups at Cβ3 position, were prepared by oneβpot coupling of secondary propargylic alcohols with 1,3βdicarbonyl compounds and __tert__βbutyl carbamate, __via__ __in situ__ deprotection of the cor