Journal
ORGANIC LETTERS
Volume 13, Issue 8, Pages 1988-1991Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol200389p
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- Max Planck Gesellschaft
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A natural product biosynthesis-inspired strategy to explore biologically relevant chemical space is presented. A phosphine-catalyzed cascade and stereoselective annulation provides a common tricyclic benzopyrone intermediate that was efficiently transformed into diverse and related naturally occurring scaffolds.
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