190005-97-1Relevant academic research and scientific papers
Synthetic studies of antitumor macrolide laulimalide: Enantioselective synthesis of the C3-C14 segment by a catalytic hetero Diels-Alder strategy
Ghosh, Arun K.,Mathivanan, Packiarajan,Cappiello, John
, p. 2427 - 2430 (2007/10/03)
The C3-C14 segment of the novel antitumor agent laulimalide has been constructed enantioselectively by utilizing a catalytic asymmetric hetero Diels-Alder reaction of benzyloxyacetaldehyde and Danishefsky's diene followed by Ferrier rearrangement and asymmetric conjugate reaction as the key steps.
