Publication | Closed Access
Total Syntheses of Murrayamine E, I, and K
65
Citations
34
References
2015
Year
Combinatorial ChemistryMedicinal ChemistryEngineeringBiochemistryLewis AcidNatural SciencesOrganic ChemistryMurrayamine ECatalysisPhenylboronic AcidChemistryHeterocycle ChemistrySynthesis MethodNatural Product SynthesisSynthetic ChemistryBiomolecular Engineering
We describe efficient synthetic routes to murrayamine A (mukoenine C), O-methylmurrayamine A, mahanine, O-methylmahanine, and murrayamine D and the first total syntheses of murrayamine E, I, and K. Key steps are a palladium-catalyzed construction of the carbazole framework and an annulation of the pyran ring, which is either catalyzed by phenylboronic acid or promoted by a Lewis acid.
| Year | Citations | |
|---|---|---|
Page 1
Page 1