作者:John H. Billman、John A. Tonnis
DOI:10.1002/jps.2600600815
日期:1971.8
hydrocinnamaldehydes, and cinnamaldehydes—was prepared and tested for antitumor activity. The substituted phenylacetaldehydes were prepared from the corresponding benzaldehydes via the Darzen glycidic ester synthesis, followed by hydrolysis and decarboxylation. The dihydrocinnamaldehydes were prepared by the lead tetraacetate oxidation of the corresponding alcohols. The cinnamaldehydes were prepared
摘要制备了一系列取代的芳烷基醛,包括取代的苯乙醛,氢肉桂醛和肉桂醛,并测试了其抗肿瘤活性。由相应的苯甲醛经Darzen缩水甘油酯合成,然后水解和脱羧,制备取代的苯基乙醛。通过相应的醇的四乙酸铅氧化制备二氢肉桂醛。肉桂醛是由取代的苯甲醛与乙基乙烯基醚反应制得的。还筛选了芳烷基醛制备中的所有中间体的抗肿瘤活性。