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ChemInform Abstract: Novel Synthetic Methodologies. Part 156. An Efficient Chemo- and Stereoselective Synthesis of Enaminones and Enaminoesters Using (Bromodimethyl)sulfonium Bromide under Solvent-Free Conditions.

✍ Scribed by Biswanath Das; Boddu Shashi Kanth; Anjoy Majhi; Kongara Ravinder Reddy

Publisher
John Wiley and Sons
Year
2009
Weight
33 KB
Volume
40
Category
Article
ISSN
0931-7597

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An efficient chemo- and stereoselective
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## Abstract (Bromodimethyl)sulfonium bromide has efficiently been employed for chemo‐ and stereoselective conversions of β‐dicarbonyl compounds into β‐enaminones and β‐enaminoesters by a treatment with amines at room temperature under solvent‐free conditions. © 2008 Wiley Periodicals, Inc. Heteroat

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## 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