alexa Solid phase versus solution phase synthesis of heterocyclic macrocycles.
Microbiology

Microbiology

Journal of Antivirals & Antiretrovirals

Author(s): Kim SJ, McAlpine SR

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Abstract Comparing a solution phase route to a solid phase route in the synthesis of the cytotoxic natural product urukthapelstatin A (Ustat A) confirmed that a solid phase method is superior. The solution phase approach was tedious and involved cyclization of a ridged heterocyclic precursor, while solid phase allowed the rapid generation of a flexible linear peptide. Cyclization of the linear peptide was facile and subsequent generation of three oxazoles located within the structure of Ustat A proved relatively straightforward. Given the ease with which the oxazole Ustat A precursor is formed via our solid phase approach, this route is amenable to rapid analog synthesis. This article was published in Molecules and referenced in Journal of Antivirals & Antiretrovirals

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