Abstract
A concise enantioselective synthesis of the fungal metabolite ent-malbrancheamide B was accomplished through the union of a C-prenylated proline derivative and a substituted indole pyruvic acid SEM enol ether, followed by a cationic double cyclization as the key step.
Original language | English |
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Pages (from-to) | 4214-4215 |
Number of pages | 2 |
Journal | Journal of the American Chemical Society |
Volume | 131 |
Issue number | 12 |
DOIs | |
Publication status | Published - 1 Apr 2009 |