作者:Konrad H. Bleicher、Fernand Gerber、Yves Wüthrich、Alexander Alanine、Alfredo Capretta
DOI:10.1016/s0040-4039(02)01839-7
日期:2002.10
Substituted imidazoles can be prepared efficiently from cyclic or acyclic 1,2-aminoalcohols via a four-step procedure involving acylation of the amine, oxidation of the alcohol, imine formation and cyclization. Examples are presented and the methodology is applied in the generation of a library of compounds containing a fused imidazole-azepine motif.
取代的咪唑可以通过包括胺的酰化,醇的氧化,亚胺的形成和环化的四步法从环状或无环的1,2-氨基醇有效地制备。给出了实施例,并将该方法应用于包含稠合的咪唑-氮杂基序的化合物的文库的产生。