Michael Addition of Thiols to α-Enones: Is Any Catalyst Necessary?
Authors: Meciarova, Maria; Toma, Stefan
Source: Letters in Organic Chemistry, Volume 3, Number 10, October 2006 , pp. 794-797(4)
Publisher: Bentham Science Publishers
Abstract:
Michael addition of thiophenol to chalcone was studied in different solvents. It was proved that reaction proceed very well in ionic liquids and chosen conventional solvents without any catalyst. It was also proved that reaction proceed well also with other thiols and other enones. Addition of selenophenol to chalcone in ethanol was also successful.Keywords: Michael addition; ionic liquids; thiols; organocatalysts
Document Type: Research article
DOI: http://dx.doi.org/10.2174/157017806779025915
Affiliations: 1: Department of Organic Chemistry, Faculty of Natural Sciences, Comenius University, 842 15 Bratislava, Slovakia.
Publication date: 2006-10-01
- Letters in Organic Chemistry publishes original letters on all areas of organic chemistry including synthesis, bioorganic, medicinal, natural products, organometallic, supramolecular, molecular recognition and physical organic chemistry. The emphasis is placed on publishing quality papers very rapidly. Letters are processed rapidly and take full advantage of the Internet technology both for the submission and the review of the manuscripts.
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- By this author: Meciarova, Maria ; Toma, Stefan

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