Abstract
(Chemical Equation Presented) The tricyclic hydroxy imidazolidinone was converted to chaetominine in seven steps in 22% overall yield. The key step was the construction of the δ-lactam by heating an amino ester with a catalytic amount of DMAP in toluene at reflux. © 2007 American Chemical Society.
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CITATION STYLE
APA
Snider, B. B., & Wu, X. (2007). Synthesis of (-)-chaetominine. Organic Letters, 9(23), 4913–4915. https://doi.org/10.1021/ol7022483
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