Stereoselective Coupling Reaction of (2Z)-β-Arylselenocinnamic Esters with Grignard Reagents in Presence of CuI
Author:
Affiliation:
1. a Department of Chemistry , Hangzhou University Hangzhou , 310028, P. R. China
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397919708007069
Reference10 articles.
1. Vinylic organoboranes. 11. A highly stereospecific and regiospecific synthesis of trisubstituted alkenes via organoboranes
2. Highly Stereoselective Synthesis of Trisubstituted (E)-Olefins Using the Base-Induced [3,3]Rearrangement ofN-Substituted β-Methallyldimethylammonium Salts in Protic Solvents
3. Wittig reactions of ylide anions derived from stabilised ylides
4. Vinylic selenides
5. Nickel and palladium catalysed coupling of vinyl selenides with trimethylsilylmethylmagnesium chloride : A new synthesis of allyl silanes
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1. Application of organic selenides and tellurides in organic synthesis;Chinese Journal of Chemistry;2010-08-27
2. ChemInform Abstract: Stereoselective Coupling Reaction of (2Z)-β-Arylselenocinnamic Esters with Grignard Reagents in Presence of CuI;ChemInform;2010-08-02
3. Synthesis of beta-phenylchalcogeno-alpha, beta-unsaturated esters, ketones and nitriles using microwave and solvent-free conditions;Journal of the Brazilian Chemical Society;2007
4. Synthesis of Se-arylmethyl selenoformates by reaction of aluminum arylmethaneselenolates with formates;Tetrahedron Letters;2005-03
5. The first synthesis of β-phenylchalcogeno-α,β-unsaturated esters via hydrochalcogenation of acetylenes using microwave and solvent-free conditions;Tetrahedron Letters;2005-03
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