Abstract
An indole synthesis via ring expansion of benzocyclobutenone oxime sulfonate was developed. Utility of the indole synthesis was demonstrated by the total synthesis of (+)-CC-1065. The middle and right segments were constructed by a sequential ring expansion of the symmetrical benzo-bis-cyclobutenone. The left segment was also constructed via ring expansion of the methyl-substituted benzocyclobutenone oxime sulfonates. After condensation of these three segments, the dienone cyclopropane structure was formed to complete the total synthesis.
Original language | English |
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Pages (from-to) | 6185-6189 |
Number of pages | 5 |
Journal | Organic Letters |
Volume | 21 |
Issue number | 16 |
DOIs | |
Publication status | Published - 2019 Aug 16 |