A unified convenient strategy for the synthesis of 5,6-dihydroxyindole-derived 2,7'-, 2,2'-, and 2,3'-biindolyls (e.g. I) is reported, which is based on proper manipulation of key o-ethynylaniline precursors. By the same methodol. 5,6-diacetoxy-7-iodoindole can also be obtained in good yield.

Efficient synthesis of 5,6-dihydroxyindole dimers, key eumelanin building blocks, by a unified o-ethynylaniline-based strategy for the construction of 2-linked biindolyl scaffolds

D'Ischia, Marco
2009

Abstract

A unified convenient strategy for the synthesis of 5,6-dihydroxyindole-derived 2,7'-, 2,2'-, and 2,3'-biindolyls (e.g. I) is reported, which is based on proper manipulation of key o-ethynylaniline precursors. By the same methodol. 5,6-diacetoxy-7-iodoindole can also be obtained in good yield.
2009
Settore CHIM/02 - Chimica Fisica
Oxidative polymerization; en-route; indoles; indolin-2-ones; derivatives; reactivity; polymers; system; anions; model
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11384/84307
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