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  4. Radical Couplings as Key Steps for the Preparation of Derivatives of Nonactic Acid
 
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Radical Couplings as Key Steps for the Preparation of Derivatives of Nonactic Acid

Auteur(s)
Loiseau, Francois
Simone, Jean-Mary
Carcache, David
Bobal, Pavel
Neier, Reinhard 
Institut de chimie 
Date de parution
2007
In
Monatsh. Chem.
Vol.
2
No
138
De la page
121
A la page
129
Mots-clés
  • Coupling reaction (ho...

  • prepn. of analogs of ...

  • a subunit of the THF ...

  • via radical coupling ...

  • nonactic acid analog ...

  • nonactin subunit anal...

Résumé
Free radical couplings from furan, as cheap starting material, were studied in view of developing a rapid strategy en route to the synthesis of derivs. of nonactin. The chain contg. the alc. function was introduced in one or two steps in 86% yield. For the introduction of the second chain with the ester function two different coupling methods were tested. Starting from the advanced intermediates obtained by this method, nonactin analogs, such s I (R = CMe3, CH2Me), were prepd. by catalytic hydrogenation of the furan ring. [on SciFinder(R)]
URI
https://libra.unine.ch/handle/123456789/21494
Type de publication
Resource Types::text::journal::journal article
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