Cyclopropamitosenes, Novel Bioreductive Anticancer Agents. Synthesis, Electrochemistry, and Biological Activity of 7-Substituted Cyclopropamitosenes and Related Indolequinones

DOI: 10.1021/jm00048a019

Source and publish data:

Journal of Medicinal Chemistry p. 3834 - 3843 (1994)

Update date:2022-09-26

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Authors:

Cotterill, Ann S.

Moody, Christopher J.

Mortimer, Roger J.

Norton, Claire L.

O'Sullivan, Noeleen

et al. et al.

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Article abstract of DOI:10.1021/jm00048a019

The synthesis of the indolequinones 8 and 9 starting from methyl 4-(benzyloxy)-5-methoxyindole-2-carboxylate (10) is described.The methoxy group in the indolequinones 1,2,4,5, and 7-9 can be displaced by various nitrogen nucleophiles (ammonia, 2-methoxyet

Full text of DOI:10.1021/jm00048a019

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Product name:xanthate 4-(benzyloxy)-5-methoxy-1-methylindole-2-methanol

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