306281-49-2Relevant academic research and scientific papers
Total Synthesis of (+)-Zaragozic Acid C
Armstrong, Alan,Barsanti, Paul A.,Jones, Lyn H.,Ahmed, Ghafoor
, p. 7020 - 7032 (2007/10/03)
A total synthesis of (+)-zaragozic acid C is described. Key features of the synthesis are the use of a double Sharpless asymmetric dihydroxylation reaction of diene 6 to control stereochemistry at four contiguous stereocenters from C3 to C6; the introduction of the C1-side chain by reaction between the anion derived from the dithiane monosulfoxide 27 and the core aldehyde 12; a high yielding, acid-mediated simultaneous acetonide deprotection-dithiane removal-ketalization procedure leading exclusively to the 2,8-dioxabicyclo[3.2.1]octane core 34; and a novel triple oxidation procedure allowing installation of the tricarboxylic acid.
Total synthesis of (+)-zaragozic acid C
Armstrong, Alan,Jones, Lyn H.,Barsanti, Paul A.
, p. 3337 - 3340 (2007/10/03)
A total synthesis of (+)-zaragozic acid C is described. Key steps are an acid-mediated acetonide deprotection-dithiane removal-ketalisation procedure, providing selectively the 2,8-dioxabicyclo[3.2.1]octane core of the natural product, and the simultaneou
