摘要
A series of novel bispyrazoles joined by arylmethylene at C-4 position were synthesized with aromatic aldehydes obtained from lignin and screened for their in vitro antioxidant activities by N,N-diphenyl-N＇picrylhydrazyl （DPPH） and 2,2＇-azino-bis（3-ethylenzothiazoline-sulphonic acid） diammonium salt （ABTS＋） radical scavenging assays. All of these compounds exhibited good DPPH and ABST＋ radical scavenging activities as compared to the standard, Trolox, which suggested their potential as promising agents for cturing tumors or other free radical-related diseases.
A series of novel bispyrazoles joined by arylmethylene at C-4 position were synthesized with aromatic aldehydes obtained from lignin and screened for their in vitro antioxidant activities by N,N-diphenyl-N＇picrylhydrazyl （DPPH） and 2,2＇-azino-bis（3-ethylenzothiazoline-sulphonic acid） diammonium salt （ABTS＋） radical scavenging assays. All of these compounds exhibited good DPPH and ABST＋ radical scavenging activities as compared to the standard, Trolox, which suggested their potential as promising agents for cturing tumors or other free radical-related diseases.
