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Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O₂ as oxidant.

ABSTRACT: The laccase-catalyzed iodination of p-hydroxyarylcarbonyl- and p-hydroxyarylcarboxylic acid derivatives using KI as iodine source and aerial oxygen as the oxidant delivers the corresponding iodophenols in a highly efficient and sustainable manner with yields up to 93% on a preparative scale under mild reaction conditions.

SUBMITTER: Sdahl M

PROVIDER: S-EPMC9065379 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Dataset Information

Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O₂ as oxidant.

OmicsDI is part of the ELIXIR infrastructure

Tweets

Dataset Information

Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O2 as oxidant.

OmicsDI is part of the ELIXIR infrastructure

Tweets

Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O₂ as oxidant.