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Propene as an Atom-Economical Linchpin for Concise Total Synthesis of Polyenes: Piericidin A.

Barry M TrostHadi Gholami
Published in: Journal of the American Chemical Society (2018)
A concise and convergent total synthesis of piericidin A is disclosed. The synthesis hinges on the utilization of propene as a synthetic linchpin to merge the properly elaborated alkyne fragments, leading to the 1,3,6-triene motif of piericidin A. Utilization of propene as a unique alkene, capable of sequential coupling with two alkynes, is further illustrated in the context of various 1,3,6-triene products. The latter process proceeds with high atom economy and efficiently gives rise to complex frameworks from readily accessible alkyne substrates. This strategic C-C bond formation offers an orthogonal paradigm in the design of synthetic routes, leading to higher step economy and more efficient syntheses of polyunsaturated natural products.
Keyphrases
  • electron transfer
  • molecular dynamics
  • fatty acid
  • room temperature
  • transition metal