637004-18-3Relevant academic research and scientific papers
Highly functionalized trans-2,5-disubstituted tetrahydrofurans from ribofuranoside templates: Precursors to linked polycyclic ethers
Dabideen, Darrin,Mootoo, David R.
, p. 8365 - 8368 (2003)
Iodoetherification of C5 allylated ribo-furanosides leads to trans-2,5-disubstituted tetrahydrofurans with high selectivity. The application of this reaction to the synthesis of complex polycyclic ethers is illustrated in the preparation of a truncated, tricyclic analog of monensin A.
