- An Ugi reaction in the total synthesis of (-)-dysibetaine.
An Ugi reaction in the total synthesis of (-)-dysibetaine.
Angewandte Chemie (International ed. in English) (2009-01-29)
Jerry Isaacson, Yoshihisa Kobayashi
PMID19173271
ABSTRACT
(-)-Dysibetaine has been synthesized in 11 steps from readily available L-malic acid (see scheme). The key step is a unique Ugi 4-center-3-component cyclization reaction, where an ester group acts as the carboxylic acid component. The use of 1,1,1,3,3,3-hexamethyldisilazane as an ammonia equivalent and a specially designed isocyanide leads to an expeditious synthesis.
MATERIALS
Product Number
Brand
Product Description
Sigma-Aldrich
Hexamethyldisilazane, produced by Wacker Chemie AG, Burghausen, Germany, ≥97.0% (GC)