919124-13-3Relevant academic research and scientific papers
Efficient and highly enantioselective formation of the all-carbon quaternary stereocentre of lyngbyatoxin A
Vital, Paulo,Tanner, David
, p. 4292 - 4298 (2006)
Indole 25, an advanced intermediate in a projected enantioselective total synthesis of lyngbyatoxin A 1, was prepared from allylic alcohol 11 in 9 steps and >95% ee, key transformations being the enantiospecific rearrangement of vinyl epoxide 14 and the H
