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Synthesis and synthetic applications of 1-donor substituted cyclopropanes with ethynyl, vinyl and carbonyl groups

  • Jacques R. Y. Salaün
Conference paper
Part of the Topics in Current Chemistry book series (TOPCURRCHEM, volume 144)

Abstract

Substituted on the same carbon by an electron donating group and an adjacent multiple bond, cyclopropanes provide building blocks of unprecedented synthetic potential. They are readily available along different routes involving: cyclopropanone hemiacetals, oxaspiropentanes, alkylidenecyclopropanes, 1-heterosubstituted lithiocyclopropanes, α-enone silyl enol ethers, 1,3-dichloroacetone and 1-hydroxycyclopropylcarbonyl derivatives as main sources.

First of all, they undergo acid-induced C3→C4 ring expansion to four-membered rings, in particular to the 2-vinylcyclobutanone system, which is an efficient precursor of C5, C6 and C8 homologous rings by subsequent acid- and base-induced, thermal, or photolytic ring enlargements. On the other hand, they undergo thermal C3→C5 ring expansion providing cyclopentanone enol ethers or derivatives with high chemo-, regio- and stereoselectivity.

Keywords

Ring Opening Vide Supra Cyclopropane Ring Ring Expansion Allylic Alcohol 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag 1988

Authors and Affiliations

  • Jacques R. Y. Salaün
    • 1
  1. 1.Laboratoire des Carbocycles, UA 478 du CNRSUniversité de Paris-SudOrsay CedexFrance

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