摘要
1-Triphenylmethyl 4 imidazolecarboxaldehyde was synthesized from fructose by ring closure, oxidation and N alkylation with an overall yield of 36.5%.
1-Triphenylmethyl 4 imidazolecarboxaldehyde was synthesized from fructose by ring closure, oxidation and N alkylation with an overall yield of 36.5%.
出处
《中国医药工业杂志》
CAS
CSCD
北大核心
2003年第12期598-599,共2页
Chinese Journal of Pharmaceuticals
关键词
1-三苯基甲基-4-咪唑甲醛
药物合成
抗癌药
中间体
1-triphenylmethyl 4 imidazolecarboxaldehyde
4 imidazolecarboxaldehyde
girolline
anticancer
intermediate
synthesis
