Palladium-Catalysed Coupling Reactions: (Z)-Vinyl (N,N-Diisopropyl)carbamate Group as an Efficient Precursor of a (Z)-Vinyl Triflate Function

ABSTRACT A (Z)-vinyl (diisopropyl)carbamate group, generated from a Hoppe allylation reaction, was easily transformed either into the corresponding (Z)-vinyl phosphate or (Z)-vinyl triflate function in good yield and high selectivity. It was also shown that the resulting (Z)-vinyl triflate compound...

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Veröffentlicht in:Synthesis (Stuttgart) 2004-12, Vol.2004 (18), p.3017-3022
Hauptverfasser: Porée, François-Hugues, Barbion, Julien, Dhulut, Sylvie, Betzer, Jean-François, Pancrazi, Ange, Ardisson, Janick
Format: Artikel
Sprache:eng
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Zusammenfassung:ABSTRACT A (Z)-vinyl (diisopropyl)carbamate group, generated from a Hoppe allylation reaction, was easily transformed either into the corresponding (Z)-vinyl phosphate or (Z)-vinyl triflate function in good yield and high selectivity. It was also shown that the resulting (Z)-vinyl triflate compound could be utilized successfully in palladium-catalysed coupling reactions with vinyl-, phenyl- and acetylenic tin derivatives, without loss of the (Z)-geometry of the double bond.
ISSN:0039-7881
1437-210X
DOI:10.1055/s-2004-834878