作者:C.F. Hammer、Robert Stevenson
DOI:10.1016/0039-128x(65)90157-1
日期:1965.5
Abstract The major product, obtained in yields up to 50% from the action of bromine on 5-dihydroergosteryl acetate (ergosta-7,22-dien-38-yl acetate) is 7,11,22a,23a-tetrabromoergost-8-en-38-yl acetate. It is accompanied by an isomer, 7,8,22a,23a-tetrabromoergost-14-enyl and other Δ 7,22 -ergostadienyl esters in described. Nuclear magnetic resonance chemical shifts of the angular methyl group protons
摘要 溴作用于乙酸 5-二氢麦角甾醇酯(ergosta-7,22-dien-38-yl acetate)的主要产物是 7,11,22a,23a-tetrabromoergost-8-en,产率高达 50%。 -38-基乙酸酯。它伴随着异构体,7,8,22a,23a-四溴麦角-14-烯基和其他描述的Δ 7,22-麦角二烯基酯。报告了代表类别的角甲基质子的核磁共振化学位移,并与计算值进行了比较。