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Decarboxylative and dehydrative coupling of dienoic acids and pentadienyl alcohols to form 1,3,6,8-tetraenes.
Deiab, Ghina'a I Abu; Al-Huniti, Mohammed H; Hyatt, I F Dempsey; Nagy, Emma E; Gettys, Kristen E; Sayed, Sommayah S; Joliat, Christine M; Daniel, Paige E; Vummalaneni, Rupa M; Morehead, Andrew T; Sargent, Andrew L; Croatt, Mitchell P.
Afiliación
  • Deiab GIA; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
  • Al-Huniti MH; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
  • Hyatt IFD; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
  • Nagy EE; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
  • Gettys KE; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
  • Sayed SS; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
  • Joliat CM; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
  • Daniel PE; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
  • Vummalaneni RM; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
  • Morehead AT; Department of Chemistry, East Carolina University, Greenville, NC 27858, USA.
  • Sargent AL; Department of Chemistry, East Carolina University, Greenville, NC 27858, USA.
  • Croatt MP; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
Beilstein J Org Chem ; 13: 384-392, 2017.
Article en En | MEDLINE | ID: mdl-28382176

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Beilstein J Org Chem Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Beilstein J Org Chem Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Alemania