ChemInform Abstract: Fluoride Ion-Mediated Peterson Alkenation of N-(C,C-Bis(trimethylsilyl) methyl)amido Derivatives with Carbonyl Compounds: A Short General Route to Enamides and 1,2-Dihydroisoquinolines.

C Palomo,M Legido,T Constantieux,J M Aizpurua,J P Picard,J Dunogues

doi:10.1002/chin.199252111

ChemInform Abstract: Fluoride Ion-Mediated Peterson Alkenation of N-(C,C-Bis(trimethylsilyl) methyl)amido Derivatives with Carbonyl Compounds: A Short General Route to Enamides and 1,2-Dihydroisoquinolines.

C Palomo, M Legido + Show 4 more

https://doi.org/10.1002/chin.199252111

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Journal: ChemInform

Publication Date: Aug 21, 2010

#Cyclic Enamides #Amido Derivatives + Show 7 more

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Abstract

Abstract A straightforward general access to diversely substituted acyclic or cyclic enamides and dienamides is accomplished by using a fluoride induced Peterson olefination of carbonyl compounds and enolizable amides derived from C,C-bis(trimethylsilyl) methylamine.

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