Synthesis of variously 2-substituted alkyl (Z)- and (E)-2-alkenoates and (Z)- and (E)-α-ylidene-γ-butyrolactones via palladium-mediated cross-coupling reactions between organostannanes and organic halides-Reference-Cited by-同舟云学术

Synthesis of variously 2-substituted alkyl (Z)- and (E)-2-alkenoates and (Z)- and (E)-α-ylidene-γ-butyrolactones via palladium-mediated cross-coupling reactions between organostannanes and organic halides

Published:1994-01 Issue:41 Volume:50 Page:12029-12046
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Bellina Fabio,Carpita Adriano,De Santis Massimo,Rossi Renzo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference55 articles.

1. For the stereoselective synthesis of trisubstituted α,β-unsaturated esters, see: Arora, A. S.; Ugi, I. K. Methoden der Organischen Chemie; Houben-Weyl, Bd. V/1b, 728–745

2. A stereoselective synthesis of (Z)- and (E)-trifluoromethylated .alpha.,.beta.-unsaturated esters via intramolecular Wittig reaction

3. Stereoselective synthesis of trisubstituted .alpha.,.beta.-unsaturated esters and amides via reactions of tantalum-alkyne complexes derived from acetylenic esters and amides with carbonyl compounds

4. Stereospecific addition of alkylcopper reagents to .alpha.,.beta.-acetylenic acids. The nature of the vinylic enolate

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