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Chin. J. Org. Chem. ›› 2003, Vol. 23 ›› Issue (10): 1102-1106. Previous Articles Next Articles
王超杰;宋金勇;赵瑾
发布日期:
Wang Chaojie;Song Jinyong;Zhao Jin
Published:
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Fourteen diacid solanesyl glycosyl esters were synthesized by the reaction of O-acetyllactopyranosyl bromide or O-acetylmaltopyranosyl bromide with diacid solanesyl monoesters, using tetrabutyl ammonium bromide as a phase-transfer catalyst. All of them are new compounds, and their structures were confirmed by IR, ~1H NMR, MS spectra and elemental analysis. Six of the target compounds were tested preliminarily in vitro for their anti-tumor activity on KB, Bel-7402 and HCT-8 cells.
Key words: LACTOSE;MALTOSE;ELEMENTAL ANALYSIS;IR;1HNMR;MS;BIOLOGICAL ACTIVITY, diacid solanesyl glycosyl ester;ANTITUMOR DRUGS
CLC Number:
R914
Wang Chaojie;Song Jinyong;Zhao Jin. Synthesis and Biological Evaluation of the Diacid Solanesyl Glycosyl Esters[J]. Chin. J. Org. Chem., 2003, 23(10): 1102-1106.
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