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Rhodium-Catalyzed Addition of Arylboronic Acids to N-Sulfonyl Aldimines
Ueda, Masato
Saito, Atsushi
Miyaura, Norio
Location: http://hdl.handle.net/2115/14624
Synlett. 2000(11), 2000, 1637-1639
http://dx.doi.org/10.1055/s-2000-7949

The addition of arylboronic acids, ArB(OH)2, to N-phenylsulfonyl aldimines, RCH=NSO2Ph (R = alkyl, aryl, 1-alkenyl), giving R(Ar)CHNHSO2Ph was carried out at 95 °C in the presence of a rhodium catalyst. [Rh(cod)(MeCN)2]BF4 (3 mol%) was found to be the best catalyst for aryl aldimines and Rh(acac)(coe)2/i-Pr3P for alkyl and 1-alkenyl aldimines. The analogous reactions of arylboronic esters, such as 1,2-ethanediol and 1,3-propanediol ester, yielded the addition products in the presence of two equivalents of Et3N.

Belongs to: Hokkaido University Collection of Scholarly and Academic Papers

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Rhodium-Catalyzed Addition of Arylboronic Acids to N-Sulfonyl Aldimines
Id. 8171150
Idioma inglés
Titulo Rhodium-Catalyzed Addition of Arylboronic Acids to N-Sulfonyl Aldimines
Autor(es) Ueda, Masato
Saito, Atsushi
Miyaura, Norio
Location http://hdl.handle.net/2115/14624
Synlett. 2000(11), 2000, 1637-1639
http://dx.doi.org/10.1055/s-2000-7949
Versión 1.0
Estado Final
Descripción The addition of arylboronic acids, ArB(OH)2, to N-phenylsulfonyl aldimines, RCH=NSO2Ph (R = alkyl, aryl, 1-alkenyl), giving R(Ar)CHNHSO2Ph was carried out at 95 °C in the presence of a rhodium catalyst. [Rh(cod)(MeCN)2]BF4 (3 mol%) was found to be the best catalyst for aryl aldimines and Rh(acac)(coe)2/i-Pr3P for alkyl and 1-alkenyl aldimines. The analogous reactions of arylboronic esters, such as 1,2-ethanediol and 1,3-propanediol ester, yielded the addition products in the presence of two equivalents of Et3N.
Tipo 113160 bytes
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Palabras clave arylboronic acids
Tipo de recurso article (author version)
Tipo de Interactividad Expositivo
Nivel de Interactividad muy bajo
Audiencia Estudiante
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Estructura Atomic
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Formatos 113160 bytes
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Fecha de contribución 26-oct-2007
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