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Enhanced reactivity of electron-deficient enynes in the palladium-catalyzed homo-benzannulation of conjugated enynes
Saito S; Chounan Y; Nogami T; Fukushi T; Tsuboya N; Yamada Y; Kitahara H; Yamamoto Y.
Afiliación
  • Saito S; Institute for Chemical Reaction Science, Tohoku University, Sendai, Japan.
J Org Chem ; 65(17): 5350-4, 2000 Aug 25.
Article en En | MEDLINE | ID: mdl-10993365
ABSTRACT
We report the high reactivity of electron-deficient enynes in the homo-benzannulation of conjugated enynes in the presence of Pd(PPh3)4. The introduction of electron-withdrawing groups enabled us to carry out the benzannulation of 1-substituted enynes as well as 1,2- and 2,4-disubstituted enynes. Polysubstituted benzenes were prepared in a highly regioselective manner in good to excellent yields.
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Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2000 Tipo del documento: Article País de afiliación: Japón
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2000 Tipo del documento: Article País de afiliación: Japón
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