915129-35-0Relevant academic research and scientific papers
Wittig rearrangement of lithiated allyl aryl ethers: A mechanistic study
Strunk, Sven,Schlosser, Manfred
, p. 4393 - 4397 (2006)
At -75°C, α-lithiated allyl phenyl ether undergoes mainly the [1,2] Wittig rearrangement to afford, after acidic hydrolysis, 1-phenyl-2-propen-1-ol as the main product. A second metalation taking place at one of the ortho positions is the sole competing s
