摘要
以(±)4,10-二氧杂三环[5,2,1,02,6]-癸-8-烯-3-醇为原料,经过芳基化、氧化、芳基化、环化、热分解和加氢反应,得到PAF新的拮抗物反式-2,5-二芳基四氢呋喃,并合成了化合物8.
A novel approach to synthesize trans-2, 5-diaryltetrahydrofuran is described. The new antagonists of PAF are obtained by six step reactions of arylation, oxidation, arylation,cyclization, hot decomposition and hydrogenation starting from (±) 4, 10-dioxatricyclo [5, 2,1, 02,6]-dec-8-ene-3-ole is described. Three title compounds (8a-8c) are synthesized.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
1998年第1期65-69,共5页
Chemical Journal of Chinese Universities
基金
中法政府科技合作项目资助
关键词
二芳基
四氢呋喃
PAF受体
反式
拮抗物
Diaryltetrahydrofuran, Antagonist, Synthesis, Chiral, Stereoselectivity