“…The CHCl 3 extract was washed with water and evaporated. The solid was chromatographed over a column of silica gel with elution by CHCl 3 :CH 3 OH (15:1) to isolate 2 (30 mg), mp 132-133°C (CH 3 OH), which was identified by direct comparison with an authentic sample on TLC [8]. The aqueous part of the hydrolysate was neutralized, condensed, and chromatographed on paper using C 5 D 5 N:C 6 H 6 :BuOH:H 2 O (3:5:1:3).…”