Stereoselective Synthesis of (1Z,3E)-2-Ethoxycarbonyl-Substituted 1,3-Dienes via Stille Coupling of (E)-α-Stannyl-α,β-Unsaturated Esters with Alkenyl Halides-Reference-Cited by-同舟云学术

Stereoselective Synthesis of (1Z,3E)-2-Ethoxycarbonyl-Substituted 1,3-Dienes via Stille Coupling of (E)-α-Stannyl-α,β-Unsaturated Esters with Alkenyl Halides

Published:2009-11-12 Issue:24 Volume:39 Page:4454-4466
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Zhao Hong¹²,Dai Ruchun¹,Cai Mingzhong¹

Affiliation:

1. a Department of Chemistry , Jiangxi Normal University , Nanchang, China

2. b Department of Pharmacy , Guangdong Pharmaceutical College , Guangzhou, China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397910902906610

Reference29 articles.

1. Asymmetric Diels-Alder and Ene Reactions in Organic Synthesis. New Synthetic Methods(48)

2. Formation of 1,3-diynes, 1,3-dienes, and biphenyls via the copper(II) nitrate mediated coupling of organotin compounds

3. The Wittig reaction: comments on the mechanism and application as a tool in the synthesis of conjugated dienes

4. Nickel- or palladium-catalyzed cross coupling. 31. Palladium- or nickel-catalyzed reactions of alkenylmetals with unsaturated organic halides as a selective route to arylated alkenes and conjugated dienes: scope, limitations, and mechanism

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2. ChemInform Abstract: Stereoselective Synthesis of (1Z,3E)-2-Ethoxycarbonyl-Substituted 1,3-Dienes via Stille Coupling of (E)-α-Stannyl-α,β-Unsaturated Esters with Alkenyl Halides.;ChemInform;2010-04-06