摘要
Selective glycosylation of the 3-OH of 5,4鈥?di-O-acetyl-kaempferol was achieved with glycosyl ortho-alkynylbenzoates as donors under the catalysis of Ph3PAuNTf2, and subsequent glycosylation of the remaining 7-OH with glycosyl trifluoroacetimidates under the catalysis of BF3路OEt2, after global deprotection, afforded the kaempferol 3,7-O-bisglycosides conveniently.