Synthesis of the enantiomer of the structure assigned to the natural product nobilisitine A

Schwartz, BrettJones, MatthewBanwell, MartinCade, Ian2015-12-101523-7060http://hdl.handle.net/1885/57860The synthesis of the enantiomer of the structure, 1, assigned to the natural product nobilisitine A has been accomplished using the enantiomerically pure cis-1,2-dihydrocatechol 4 as starting material. The1H and13C NMR spectral data derived from compoundKeywords: alkaloid; biological product; fused heterocyclic rings; nobilisitine A; angiosperm; article; chemical structure; chemistry; nuclear magnetic resonance; stereoisomerism; synthesis; Alkaloids; Biological Products; Heterocyclic Compounds with 4 or More RingsSynthesis of the enantiomer of the structure assigned to the natural product nobilisitine A201010.1021/ol102249q2016-02-24