摘要:
The first 3-(3-pyrazolyl)indole-N-glycosides were prepared starting from indole-Nglycosides by conversion with 4-ethoxy-1,1,1-trifluorobut-3-en-2-one and following cyclization with hydrazine. The cytotoxic activity of the products against human keratinocytes (HaCaT) was studied.