1887

oa South African Journal of Chemistry - Synthesis of a structurally constrained endoperoxide having antimalarial activity from -Santonin

Volume 58, Issue 1
  • ISSN : 0379-4350

 

Abstract

-Santonin 3 was successfully converted into a biologically active compound 5b containing an endoperoxide group through a photo-oxygenation approach as a single isomer. It was found that the singlet oxygen afforded the isomer produced by attack from the sterically-hindered face of cyclohexadiene derivative 4. Evidence to this end is presented based on NOE results and the products formed in the photo-oxygenation reaction, as well as the testing of 5b for antimalarial activity.

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/content/chem/58/1/EJC24369
2005-01-01
2016-12-10

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