Wittig Olefination between Phosphine, Aldehyde, and Allylic Carbonate: A General Method for Stereoselective Synthesis of Trisubstituted 1,3-Dienes with Highly Variable Substituents-Reference-Cited by-同舟云学术

Wittig Olefination between Phosphine, Aldehyde, and Allylic Carbonate: A General Method for Stereoselective Synthesis of Trisubstituted 1,3-Dienes with Highly Variable Substituents

Published:2010-01-27 Issue:5 Volume:12 Page:976-979
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhou Rong¹,Wang Chunzhang¹,Song Haibin¹,He Zhengjie¹

Affiliation:

1. The State Key Laboratory of Elemento-Organic Chemistry and Department of Chemistry, Nankai University, 94 Weijin Road, Tianjin 300071, P. R. China, and School of Chemistry and Chemical Engineering, Henan University, 85 Minglun Street, Kaifeng 475001, P. R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol902956y

Reference58 articles.

1. Functionalized 1‐Alkoxy‐1,3‐dienes: Their Preparation and Applications in Synthetic Organic Chemistry

2. The Diels-Alder Reaction in Total Synthesis

3. Neodymium-Based Ziegler/Natta Catalysts and their Application in Diene Polymerization

4. Rare-Earth Metals and Aluminum Getting Close in Ziegler-Type Organometallics

5. Recent Advances in Efficient and Selective Synthesis of Di-, Tri-, and Tetrasubstituted Alkenes via Pd-Catalyzed Alkenylation−Carbonyl Olefination Synergy

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