1408078-65-8Relevant articles and documents
Optimization of Grignard ring-opening of α-brominated dioxolanes for the preparation of β-hydroxy-protected vinyl ethers by a three-step one-pot procedure
André, Mathieu,Letribot, Boris,Bayle, Martine,Mounetou, Emmanuelle,Chezal, Jean-Michel
, p. 6107 - 6110 (2012/11/07)
Aliphatic, cyclic, and aromatic benzoate-protected γ-hydroxy enol ethers were prepared from α-brominated dioxolanes by a three-step reaction procedure and a one-pot protocol involving Grignard reagent formation, ring-opening, and final benzoate protection