Journal
ORGANIC LETTERS
Volume 16, Issue 19, Pages 4980-4983Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol502177m
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Applying a biomimetic approach, the first total synthesis of (+/-)-tubastrindole B is reported herein. This work features a ring-expansion cascade of a dictazole-type precursor into cycloaplysinopsin-type congeners. Moreover, the isolation of a transient biogenetic intermediate represents a milestone in the biosynthetic understanding of this family of marine alkaloids.
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