868944-84-7Relevant academic research and scientific papers
A tandem C-H insertion-acetal cleavage sequence: Stereocontrolled synthesis of substituted tetrahydrofurans
Garbi, Amel,Mina, John G.,Steel, Patrick G.,Longstaff, Tim,Vile, Sadie
, p. 7175 - 7178 (2005)
A short sequence involving Rh(II) mediated carbene insertion followed by Lewis acid promoted reductive acetal cleavage with Et3SiH provides a stereoselective method for the construction of 2,3,5-trisubstituted tetrahydrofuran rings.
