Extended scope of the grignard reaction of β-haloacetals. Use of acyclic acetals
1989; Elsevier BV; Volume: 30; Issue: 27 Linguagem: Inglês
10.1016/s0040-4039(00)99436-x
ISSN1873-3581
Autores Tópico(s)Synthesis and Reactions of Organic Compounds
ResumoCareful control of reaction conditions permits the high yield preparation of Grignard reagents from β-halogenoacetals and their condensation with carbonyl compounds, regardless of the halogen (bromine, chlorine) or acetal structure (cyclic, acyclic).
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