Catalytic Cascade Reactions Inspired by Polyketide Biosynthesis

Authors

  • Daniel Moser University of Basel, Department of Chemistry, St. Johanns-Ring 19, CH-4056 Basel
  • Alessandro Castrogiovanni University of Basel, Department of Chemistry, St. Johanns-Ring 19, CH-4056 Basel
  • Dominik Lotter University of Basel, Department of Chemistry, St. Johanns-Ring 19, CH-4056 Basel
  • Reto M. Witzig University of Basel, Department of Chemistry, St. Johanns-Ring 19, CH-4056 Basel
  • Vincent C. Fäseke University of Basel, Department of Chemistry, St. Johanns-Ring 19, CH-4056 Basel
  • Felix C. Raps University of Basel, Department of Chemistry, St. Johanns-Ring 19, CH-4056 Basel
  • Christof Sparr University of Basel, Department of Chemistry, St. Johanns-Ring 19, CH-4056 Basel;, Email: christof.sparr@unibas.ch

DOI:

https://doi.org/10.2533/chimia.2020.699

PMID:

32958107

Keywords:

Aldol condensation, Atropisomers, Biomimetic synthesis, Late-stage catalysis, Stereoselectivity

Abstract

Aldol reactions belong to the most important methods for carbon–carbon bond formation and are also involved in one of the most astonishing biosynthetic processes: the biosynthesis of polyketides governed by an extraordinarily sophisticated enzymatic machinery. In contrast to the typical linear or convergent strategies followed in chemical synthesis, this late-stage catalysis concept allows Nature to assemble intermediates that are diversified into a broad range of scaffolds, which assume various crucial biological functions. To transfer this concept to small-molecule catalysis to access products beyond the natural systems, a stepwise approach to differentiate increasingly complex substrates was followed by investigating arene-forming polyketide cyclizations. An outline of our efforts to develop and apply these concepts are presented herein.

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Published

2020-09-30

How to Cite

[1]
D. Moser, A. Castrogiovanni, D. Lotter, R. M. Witzig, V. C. Fäseke, F. C. Raps, C. Sparr, Chimia 2020, 74, 699, DOI: 10.2533/chimia.2020.699.