AN EASY CONVERSION OF THE BAYLIS-HILLMAN ADDUCTS INTO tert-BUTYLDIMETHYLSILYL ETHERS WITH tert-BUTYLDIMETHYLSILYL CHLORIDE AND Li2S
Author:
Affiliation:
1. a Department of Chemistry, Faculty of Sciences, Guilan University , Rasht, Iran
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10426500490485291
Reference27 articles.
1. Chiral Amine-Catalyzed Asymmetric Baylis−Hillman Reaction: A Reliable Route to Highly Enantiomerically Enriched (α-Methylene-β-hydroxy)esters
2. The Baylis-Hillman reaction: A novel carbon-carbon bond forming reaction
3. Baylis–Hillman chemistry: a novel synthesis of functionalized 1,4-pentadienes
4. Applications of Baylis–Hillman chemistry: enantioselective synthesis of (−)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy
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1. One-pot conversion of carbamates of unsaturated β-aminoesters into unsaturated β-lactams by use of trimethylsilyl iodide;Phosphorus, Sulfur, and Silicon and the Related Elements;2016-07-29
2. Transformations of Functional Groups in Morita–Baylis–Hillman Adducts;The Chemistry of the Morita-Baylis-Hillman Reaction;2011-04-04
3. Recent Contributions from the Baylis−Hillman Reaction to Organic Chemistry;Chemical Reviews;2010-08-24
4. One-pot facile conversion of Baylis-Hillman adducts into 1,5-diarylpyrazoles using microwave irradiation;Journal of the Iranian Chemical Society;2006-03
5. An Easy Conversion of the Baylis?Hillman Adducts into tert-Butyldimethylsilyl Ethers with tert-Butyldimethylsilyl Chloride and Li2S.;ChemInform;2005-04-26
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