Alkylation of diethyl acetamidomalonate by weak electrophiles

Article abstract of DOI:10.1080/00397919508010809

Diethyl acetamidomalonate was efficiently alkylated with electrophiles of low reactivity under modified phase transfer-catalysis conditions in the absence of organic solvent using potassium ten-butoxide as a base.

Full text of DOI:10.1080/00397919508010809

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Synthetic Communications: An
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Organic Chemistry
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Alkylation of Diethyl
Acetamidomalonate by Weak
Electrophiles
Jiarong Zhu a , Hervc Galons a , Philippe Pigeon b
André Loupy b
&
a Laboratoire de Chimie Organique, FaculteÉ de
Pharmacie, 4, avenue de l′Observatoire, 75270,
Paris, France
b Laboratoire des Reéactions Seélectives sur
Supports, ICMO, UA 478, CNRS Universiteé de Paris
Sud, Ba[acaron] 410, Orsay Ceédex, France
Available online: 23 Sep 2006
To cite this article: Jiarong Zhu, Hervc Galons, Philippe Pigeon & André Loupy
(1995): Alkylation of Diethyl Acetamidomalonate by Weak Electrophiles, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 25:2, 215-218
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