The total synthesis of corallopyronin A and myxopyronin B

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  • Helmholtz Centre for Infection Research (HZI)
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Details

Original languageEnglish
Pages (from-to)11381-11384
Number of pages4
JournalAngewandte Chemie - International Edition
Volume51
Issue number45
Publication statusPublished - 5 Nov 2012

Abstract

Leading the way: The synthesis of natural products with new biological targets is one of the driving forces for the development of new antibiotics. The synthesis of the two secondary metabolites corallopyronin and myxopyronin (see picture) have been achieved, which are prominent leads for the inhibition of bacterial RNA polymerase.

Keywords

    corallopyronin, myxobacteria, protecting groups, RNA polymerase, Walsh coupling

ASJC Scopus subject areas

Cite this

The total synthesis of corallopyronin A and myxopyronin B. / Rentsch, Andreas; Kalesse, Markus.
In: Angewandte Chemie - International Edition, Vol. 51, No. 45, 05.11.2012, p. 11381-11384.

Research output: Contribution to journalArticleResearchpeer review

Rentsch A, Kalesse M. The total synthesis of corallopyronin A and myxopyronin B. Angewandte Chemie - International Edition. 2012 Nov 5;51(45):11381-11384. doi: 10.1002/anie.201206560
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