Total Mycosynthesis: Rational Bioconstruction and Bioengineering of Fungal Natural Products

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Original languageEnglish
Pages (from-to)2381-2394
Number of pages14
JournalSYNTHESIS-STUTTGART
Volume53
Issue number14
Early online date26 Feb 2021
Publication statusPublished - 20 Jul 2021

Abstract

Total biosynthesis in fungi is beginning to compete with traditional chemical total synthesis campaigns. Herein, the advantages, disadvantages and future opportunities are discussed within the scope of several recent examples. 1 Introduction 2 Synthetic Examples 2.1 2-Pyridones 2.2 Cytochalasans 2.3 Sorbicillinoids 2.4 Decalins: Solanapyrone 2.5 α-Pyrone Polyenes: Citreoviridin and Aurovertin 2.6 Anditomin and Related Meroterpenoids 2.7 Tropolone Sesquiterpenoids 3 Conclusion.

Keywords

    pyridone, cytochalasan, sorbicillinoid, decalin, alpha-pyrone, meroterpenoid, tropolone sesquiterpenoid, α-pyrone

ASJC Scopus subject areas

Cite this

Total Mycosynthesis: Rational Bioconstruction and Bioengineering of Fungal Natural Products. / Kahlert, Lukas; Schotte, Carsten; Cox, Russell J.
In: SYNTHESIS-STUTTGART, Vol. 53, No. 14, 20.07.2021, p. 2381-2394.

Research output: Contribution to journalArticleResearch

Kahlert L, Schotte C, Cox RJ. Total Mycosynthesis: Rational Bioconstruction and Bioengineering of Fungal Natural Products. SYNTHESIS-STUTTGART. 2021 Jul 20;53(14):2381-2394. Epub 2021 Feb 26. doi: 10.1055/a-1401-2716
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