Artigo Revisado por pares

Reaction of methylcerium reagent with tertiary amides: Synthesis of saturated and unsaturated ketones from tertiary amides

1998; Elsevier BV; Volume: 39; Issue: 27 Linguagem: Inglês

10.1016/s0040-4039(98)00959-9

ISSN

1873-3581

Autores

Michio Kurosu, Yoshito Kishi,

Tópico(s)

Chemical Synthesis and Analysis

Resumo

The reaction of CeCl3•MeLi to tertiary amides has been studied. The reagent prepared from cerium(III) chloride and methyllithium at 0 °C adds cleanly to morpholine amides to give the corresponding methyl ketones. Even in the presence of a large excess of the reagent, no tertiary alcohol formation is observed, indicating that the tetrahedral intermediates are stable under the reaction conditions employed.

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