Stereoselective construction of polyhydroxyalkyl 2-thiazolyl ketones (thiazole ketoses) from d-glyceraldehyde and d-arabinose acetonides by wittig-michael sequence. a route to d-gluco-KDO
作者:Alessandro Dondoni、Pedro Merino、Jesús Orduna
DOI:10.1016/s0040-4039(00)79735-8
日期:1991.7
The carbonylolefination of the title alkoxy aldehydes by 2-thiazolecarbonylmethylenetriphenyl-phosphorane 3 affords the corresponding (E)-enones which undergo syn-diastereoselective (ds, 85-95%) 1,4-conjugate addition of benzyl oxide anion; acid-catalyzed methanolysis of polyalkoxyalkyl ketones obtained in that way gives methyl 1-(2-thiazolyl)pyranoside precursors to ulosonic acids.
Dondoni, Alessandro; Marra, Alberto; Merino, Pedro, Journal of the American Chemical Society, 1994, vol. 116, # 8, p. 3324 - 3336
作者:Dondoni, Alessandro、Marra, Alberto、Merino, Pedro