56588-25-1Relevant academic research and scientific papers
Molecular rearrangement of D:A-friedoolean-6β,7β-epoxide
Mukherjee, J,Banerjee, Reena,Sayeed, Abu,Duttagupta, A
, p. 659 - 663 (2007/10/02)
D:A-Friedoolean-6β,7β-epoxide (I) undergo molecular rearrangement on treatment with dry hydrogen chloride in chloroform to afford the non-conjugated diene (VI).Treatment of I with boron trifluoride etherate in benzene furnish the enol (X) while with aq. perchloric acid in tetrahydrofuran the diol (XII) and the enol (X) are obtained.
