4.6 Article

A rapid stereocontrolled synthesis of the 3a-hydroxy-pyrrolo[2,3-b]indole skeleton, a building block for 10b-hydroxy-pyrazino[1 ',2 ': 1,5]pyrrolo[2,3-b]indole-1,4-diones

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 1, Issue 20, Pages 3492-3494

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b308288a

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A two-step selenocyclisation-oxidative deselenation sequence was used to establish the 3a-hydroxy-pyrrolo-[2,3-b]indole core; these tricycles were used as effective precursors to 10b-hydroxy-pyrazino[1',2' : 1,5]pyrrolo-[2,3-b]indole-1,4-diones.

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