1008796-65-3Relevant academic research and scientific papers
Lewis acid promoted Mukaiyama aldol-Prins (MAP) cyclizations of acetals, ketals, α-acetoxy ethers, and orthoformates
Gesinski, Michael R.,Van Orden, Lori J.,Rychnovsky, Scott D.
, p. 363 - 366 (2008)
The Mukaiyama aldol-Prins (MAP) cyclization of acetals stereoselectively provided substituted tetrahydropyrans. The scope of the reaction has been expanded to include other electrophiles, including ketals and α-acetoxy ethers. Finally, a double MAP cycliz
