3-Acetoxy-2-dimethylphosphonoacrylates. New Dienophiles and Their Use for the Synthesis of Carbocyclic C-Nucleoside Precursors by the Aid of RRA Reaction-Reference-Cited by-同舟云学术

3-Acetoxy-2-dimethylphosphonoacrylates. New Dienophiles and Their Use for the Synthesis of Carbocyclic C-Nucleoside Precursors by the Aid of RRA Reaction

Published:1990-10 Issue:10 Volume:19 Page:1855-1858
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Katagiri Nobuya,Yamamoto Mitsuo,Kaneko Chikara

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/19/10/19_10_1855/_pdf

Reference16 articles.

1. 1,3-Dipolar cycloaddition of di-1-menthyl benzylidenemalonate to (z)n,α-diphenylnitrone: Explanation for diastereoselectivity

2. Carbocyclic nucleosides

3. Phosphonic Acids and Esters. XVII. Formation, Aromatization, and Reduction of Diels—Alder Adducts of Vinyl- and Chlorovinylphosphonates1

4. Bicyclo[2,2,1]heptylphosphonates II. Stéréochimie de l'addition de Diels–Alder du vinylphosphonate de diméthyle sur quelques cyclopentadiènes; étude par r.m.n.

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