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Total synthesis of indole-3-acetonitrile-4-methoxy-2-C-?-D-glucopyranoside. Proposal for structural revision of the natural product.

ABSTRACT: Indole-3-acetonitrile-4-methoxy-2-C-?-D-glucopyranoside (1), a novel C-glycoside from Isatis indigotica with important cytotoxic activity, has been prepared in ten steps from ethynyl-?-C-glycoside 3 and 2-iodo-3-nitrophenyl acetate 6. Key steps in the synthesis include a Sonogashira coupling and a CuI-mediated indole formation. NMR spectroscopic data for synthetic 1 differs from that reported for the natural product. A revised structure for the natural product, containing an alternate carbohydrate substituent, is proposed.

SUBMITTER: Yepremyan A 

PROVIDER: S-EPMC3388122 | biostudies-literature | 2012 Jul

REPOSITORIES: biostudies-literature

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Total synthesis of indole-3-acetonitrile-4-methoxy-2-C-β-D-glucopyranoside. Proposal for structural revision of the natural product.

Yepremyan Akop A   Minehan Thomas G TG  

Organic & biomolecular chemistry 20120612 27

Indole-3-acetonitrile-4-methoxy-2-C-β-D-glucopyranoside (1), a novel C-glycoside from Isatis indigotica with important cytotoxic activity, has been prepared in ten steps from ethynyl-β-C-glycoside 3 and 2-iodo-3-nitrophenyl acetate 6. Key steps in the synthesis include a Sonogashira coupling and a CuI-mediated indole formation. NMR spectroscopic data for synthetic 1 differs from that reported for the natural product. A revised structure for the natural product, containing an alternate carbohydra  ...[more]

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