Intramolecular Oxidative Coupling of the Bis Enolate Derived from Dimethyl β,β-Dimethylglutarate: A Facile Stereoselective Route to a Versatile Synthon for Preparation of Insecticidal Pyrethroids-Reference-Cited by-同舟云学术

Intramolecular Oxidative Coupling of the Bis Enolate Derived from Dimethyl β,β-Dimethylglutarate: A Facile Stereoselective Route to a Versatile Synthon for Preparation of Insecticidal Pyrethroids

Published:1983-09 Issue:11 Volume:13 Page:905-911
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Babler James H.,Haack Richard A.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397918308059544

Reference10 articles.

1. Preparation and Diels-Alder Reactions of Hetero-Substituted 1,3-Dienes

2. 3-Triethylsilyloxypentadienyllithium, a Versatile 1,3-Diene- or Vinyl Ketone-Building Block

3. Natural product synthesis via allylsilanes. 1. Synthesis and reactions of (1E,3E)-4-acetoxy-1-(trimethylsilyl)-1,3-butadiene and its use in the total synthesis of (.+-.)-shikimic acid

4. Reactions of Ketene Acetals; 121. A Regiospecific Synthesis of Anthragallols

5. Alkoxy-5 pentadienoates : etude de leur reactivite dans la reaction de diels et alder sous haute pression

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