6533b872fe1ef96bd12d36af
RESEARCH PRODUCT
Synthesis and Reactivity of New β-Enamino Acid Derivatives: A Simple and General Approach to β-Enamino Esters and Thioesters
Antonio Hidalgo NavarroAntonio Simon FuentesViviana JofreMarta Garcia De La TorreJuan Server CarrioRaquel Pérez CarlónSantos Fusterosubject
chemistry.chemical_compoundchemistrySimple (abstract algebra)Organic ChemistryImidazoleAcid hydrolysisReactivity (chemistry)Combinatorial chemistrydescription
A new strategy has been developed for the synthesis of several β-enamino acid derivatives. N,N‘-Carbonyldiimidazole has been used as C-acylating agent of methyl ketimines, providing a direct and simple route to new β-enamino carbonyl imidazole derivatives 2. These derivatives 2 were cleanly and efficiently transformed into β-enamino esters 4 (X = O) and thioesters 4 (X = S) by reaction with a great variety of alcohols and thiols, including tertiary ones. Alternative and complementary routes to compounds 4 were also investigated. In addition, β-keto esters 6 have been obtained by mild acid hydrolysis of β-enamino esters 4.
year | journal | country | edition | language |
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1998-11-01 | The Journal of Organic Chemistry |