Answers are grounded in this paper and cite their sources.
A concise synthesis of maremycins A and D1 has been accomplished via cycloaddition of a chiral cyclic nitrone with ( E)-3-ethylidene-1-methylindolin-2-one as a key step. This synthesis clarifies the stereochemistry of the maremycins and is suitable for large-scale synthesis for biological screening.
No takes yet. Share an insight, caveat, or question.
Ueda et al. (2008) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: