1,3-Dipolar cycloaddition reactions of pyrazolidinium ylides with vinyl sulfones. A regioselective synthesis of bicyclic pyrazolidinone antibacterial agents-Reference-Cited by-同舟云学术

1,3-Dipolar cycloaddition reactions of pyrazolidinium ylides with vinyl sulfones. A regioselective synthesis of bicyclic pyrazolidinone antibacterial agents

Published:1988-01 Issue:11 Volume:44 Page:3119-3126
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Jungheim Louis N.,Barnett Charles J.,Gray Joseph E.,Horcher Linus H.,Shepherd Timothy A.,Sigmund Sandra K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference20 articles.

1. Bicyclic pyrazolidinones, a new class of antibacterial agent based on the β-lactam model

2. Bicyclic pyrazolidinones, steric and electronic effects on antibacterial activity

3. 1,3-Dipolar cycloaddition reactions of pyrazolidinium ylides with acetylenes. Synthesis of a new class of antibacterial agents

4. Dienophilic properties of phenyl vinyl sulfone and trans-1-(phenylsulfonyl)-2-(trimethylsilyl)ethylene. Their utilization as synthons for ethylene, 1-alkenes, acetylene, and monosubstituted alkynes in the construction of functionalized six-membered rings via [4 + 2] .pi. cycloaddition methodology

5. Selectivity in cycloadditions—XI

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