108733-36-4Relevant academic research and scientific papers
Regioselective SN' allylic substitution versus 1,4-addition: Synthesis of α-substituted β,γ-unsaturated esters
Girard,Romain,Ahmar,Bloch
, p. 7399 - 7402 (2007/10/02)
The reaction of the higher order organocuprate reagents R2Cu(CN)Li2-BF3 with γ-bromo α,β-unsaturated esters gives with very high selectivity α-substituted β,γ-unsaturated esters arising from a SN' allylic substitution. This reaction allows an easy access to α-silyl β,γ-unsaturated esters.
Regioselective Carboxylation of Silicon-Stabilized Allylic Carbanions and the Synthetic Utility of 2-Silyl-3-butenoates
Uno, Hidemitsu
, p. 2471 - 2480 (2007/10/02)
Carbanions of allylic dimethylphenylsilanes show remarkable regioselectivity toward carboxylation with carbon dioxide and methylation with methyl iodide.Methylationn of these compounds occurred preferentially at α position, although allyltrimethylsilane and allyltriphenylsilane are known to give γ selectivity toward the same electrophiles.Moreover, their aluminum "ate" complexes react with carbon dioxide regioselectively at the α position irrespective of methyl substitution pattern of the allylic moieties.The α-carboxylated allylic silanes proved to be useful synthons of 3-(methoxycarbonyl)allyl anions after esterifiaction.
