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Journal ArticleDOI

A biomimetic route to the peptide alkaloid anachelin.

Karl Gademann, +1 more
- 21 Jun 2004 - 
- Vol. 43, Iss: 25, pp 3327-3329
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TLDR
Experiments with a model substrate indicate that it is likely that a catechol oxidase-type enzyme is involved in the biosynthesis of the anachelin chromophore.
Abstract
A postulated biogenesis forms the basis for a synthetic route to the natural product anachelin H. Key steps include a tellurium-mediated, oxidative aza annulation and a Claisen condensation under mild conditions. Experiments with a model substrate indicate that it is likely that a catechol oxidase-type enzyme is involved in the biosynthesis of the anachelin chromophore.

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Journal ArticleDOI

An alternative approach to the synthesis of the three fragments of anachelin H

TL;DR: The synthesis of the fully protected peptide, polyketide and alkaloid fragments of anachelin H is presented to allow more efficient biological studies on the fragments instead of the whole natural product.
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