## Abstract magnified image Several tetrasubstituted NH pyrroles, functionalized with ester or ketone groups at C‐3 position, were prepared by one‐pot coupling of secondary propargylic alcohols with 1,3‐dicarbonyl compounds and __tert__‐butyl carbamate, __via__ __in situ__ deprotection of the cor
ChemInform Abstract: One-Pot Three-Component Synthesis of Tetrasubstituted N—H Pyrroles from Secondary Propargylic Alcohols, 1,3-Dicarbonyl Compounds and tert-Butyl Carbamate.
✍ Scribed by Victorio Cadierno; Jose Gimeno; Noel Nebra
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 28 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0931-7597
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## Abstract A simple and highly efficient method for the preparation of fully substituted pyrroles, from readily accessible secondary propargylic alcohols, 1,3‐dicarbonyl compounds and primary amines, has been developed. The one‐pot multicomponent reaction, which is catalysed by the system [Ru(η^3^
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v