75404-02-3Relevant academic research and scientific papers
An Improved Route to an Intermediate in Podophyllotoxin Synthesis
Murphy, William S.,Wattanasin, Sompong
, p. 262 - 263 (1980)
Cyclopropanation of the chalcone (3) with dimethylsulfonium ethoxycarbonylmethylide affords a 1:1 mixture of the cyclopropanyl keto-ester epimers (4) and (5); both stannic chloride and boron trifluoride etherate in nitromethane catalyse the stereoselective cyclisation of this mixture to the tetralone (2), the known podophyllotoxin precursor, in 51percent overall yield.
