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Synthesis of Functionalized Allylsilicone Compounds via Rhodium-Catalyzed Conjugate Addition of (E)- or (Z)-[3-Trimethylsilyl-1-propenyl]boronic Acids to Enones
Yamamoto, Yasunori
Fujita, Masayoshi
Miyaura, Norio
Location: http://hdl.handle.net/2115/14625
Synlett. 2000(5), 2002, 767-768

The rhodium-catalyzed conjugate addition of (E)-Me3SiCH2CH=CHB(OiPr)2 or (Z)-Me3SiCH2(C4H9)C=CHB(OiPr)2 to enones provided a novel method for the synthesis of allylsilicone compounds possessing a carbonyl group in the same molecule, which are versatile intermediates for intramolecular allylsilylation, giving cyclobutanols on treatment with Bu4NF.

Belongs to: Hokkaido University Collection of Scholarly and Academic Papers

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Synthesis of Functionalized Allylsilicone Compounds via Rhodium-Catalyzed Conjugate Addition of (E)- or (Z)-[3-Trimethylsilyl-1-propenyl]boronic Acids to Enones
Id. 8171151
Idioma inglés
Titulo Synthesis of Functionalized Allylsilicone Compounds via Rhodium-Catalyzed Conjugate Addition of (E)- or (Z)-[3-Trimethylsilyl-1-propenyl]boronic Acids to Enones
Autor(es) Yamamoto, Yasunori
Fujita, Masayoshi
Miyaura, Norio
Location http://hdl.handle.net/2115/14625
Synlett. 2000(5), 2002, 767-768
Versión 1.0
Estado Final
Descripción The rhodium-catalyzed conjugate addition of (E)-Me3SiCH2CH=CHB(OiPr)2 or (Z)-Me3SiCH2(C4H9)C=CHB(OiPr)2 to enones provided a novel method for the synthesis of allylsilicone compounds possessing a carbonyl group in the same molecule, which are versatile intermediates for intramolecular allylsilylation, giving cyclobutanols on treatment with Bu4NF.
Tipo 92777 bytes
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Palabras clave allylsilicone
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 92777 bytes
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Fecha de contribución 26-oct-2007
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