DIASTEREOSELECTION IN A DIRECTED CROSSED ALDOL REACTION BETWEEN TWO POLYOXYGENATED KETONES EMPLOYING TIN(II) ENOLATES. A FACILE STEREOSELECTIVE SYNTHESIS OF ETHYL 2-<i>C</i>-METHYL-DL-LYXOFURANOSIDE
作者:Rodney W. Stevens、Teruaki Mukaiyama
DOI:10.1246/cl.1983.595
日期:1983.4.5
Tin(II) enolates of 1,3-dihydroxy-2-propanone derivatives react with a second ketone, methyl pyruvate, under mild conditions to afford the corresponding anti-crossed aldol products in moderate to excellent yields. Facile elaboration to the branched-chainsugar, ethyl 2-C-methyl-DL-lyxofuranoside, was demonstrated.
1,3-二羟基-2-丙酮衍生物的锡 (II) 烯醇化物与第二种酮丙酮酸甲酯在温和条件下反应,以中等至极好的产率提供相应的抗交叉羟醛产物。证明了对支链糖乙基 2-C-甲基-DL-lyxofuranoside 的简单加工。