938071-27-3Relevant academic research and scientific papers
Total synthesis of siphonazole and its O-methyl derivative, structurally unusual bis-oxazole natural products
Linder, Joerg,Blake, Alexander J.,Moody, Christopher J.
experimental part, p. 3908 - 3916 (2009/06/28)
The details of the first syntheses of the unusual bis-oxazole natural products siphonazole and its O-methyl derivative are reported. The cinnamyl substituted oxazole was constructed using diazocarbonyl chemistry, whereby the cinnamamide was reacted with the rhodium carbene derived from methyl 2-diazo-3-oxobutanoate to give a β-ketoamide that was cyclodehydrated to the corresponding oxazole-4-ester. Reduction to the corresponding aldehyde was followed by coupling with a zinc reagent derived from methyl 2-iodomethyl-5-methyloxazole-4-carboxylate, also prepared using rhodium carbene chemistry, to give, after oxidation of the resulting secondary alcohol, the desired bis-oxazole ketone. The syntheses were completed by hydrolysis of the ester and coupling of the 2,4-pentadienylamine side chain. The 2008 Royal Society of Chemistry.
The total synthesis of siphonazole, a structurally unusual bis-oxazole natural product
Linder, Joerg,Moody, Christopher J.
, p. 1508 - 1509 (2008/02/03)
The first synthesis of the unusual bis-oxazole natural product siphonazole is reported, both oxazole rings being constructed using rhodium carbene chemistry. The Royal Society of Chemistry.
