Facile Baylis-Hillman reaction of substituted 3-isoxazolecarbaldehydes: The impact of proximal heteroatom within a heterocycle on the acceleration of reaction
Data(s) |
15/11/2007
15/11/2007
2003
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Resumo |
The fast and facile Baylis-Hillman reaction in substi-tuted 3-isoxazolecarbaldehydes confirms the impact of the proxi-mal heteroatom within a heterocycle towards enhanced reactivity of the formyl group for this reaction |
Formato |
110654 bytes application/pdf |
Identificador |
Synthesis(2003), 2325-2330 |
Idioma(s) |
en |
Relação |
CDRI Communication No. 6430 |
Palavras-Chave | #Baylis-Hillman reaction #3-isoxazolecarbaldehyde #DABCO #DMAP |
Tipo |
Article |