Answers are grounded in this paper and cite their sources.
Rapid access: An expeditious synthesis of hippuristanol was developed that allowed rapid access to a number of analogues with structural alteration at its E and F rings (see scheme), facilitating the structure–activity relationship studies of the novel inhibitor of eukaryotic translation initiation.
No takes yet. Share an insight, caveat, or question.
Li et al. (2009) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: