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假蜜环菌甲素合成方法的改进 被引量:2

Improved Synthesis of Armillarisin A
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摘要 假蜜环菌甲素是从夜间发光的柳树朽木上生长的蜜环菌培养液中分离的荧光物质,化学结构为3-乙酰基-5-羟甲基-7-羟基-香豆素(Ⅵ)。该药兼有利胆、解痉、止痛、消炎等多种作用,可单独用于治疗非严重梗阻型急性胆道感染,其特点为起效快、活性高。 Much improvement was made in the synthesis of Armillarisin A. Our first efforts were focussed on developing an alternative and efficient method for the preparation of the key intermediate, 5-hydroxymethyl-resorcinal by lithium aluminium hydride reduction of methyl 3,5-diacetoxybenzoate, the yieldof this step being 84%. The final cyclization of 5-hydroxymethyl-resorcinal with one molar equivalent of methyl ethoxymethylene acetylacetate in the presence of sodium t-butoxide produced the Armillarisin A was in 76% yield.
作者 王尔华
出处 《中国药科大学学报》 CAS CSCD 北大核心 1991年第4期236-237,共2页 Journal of China Pharmaceutical University
关键词 假蜜环菌甲素 香豆素类 合成 Armillarisin A 3-Acetyl-5-hydroxymethyl-7-hydroxy-coumarin Choleretic drug
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  • 1袁明生,孙佩琼.四川蕈菌[M].第1版.成都:四川科技出版社,1994:412.
  • 2江苏“亮菌”科研协作组微生物小组.假蜜环菌的研究.微生物学报,1974,14(1):5-5.
  • 3Jones AJ, Grant DM. Carbon - 13 magnetic resonance.XVII. pyrimidine and purine nucleosides[J].Journal of American Chemical Society, 1970, 92(6) : 4 079.
  • 4Higuchi R, Inagaki M, Togawa K, et al. Isolation and structure of cerebrosides from the sea cucumber Pentacta australis [J ] . Liebigs Annalen der Chernie , 1994, 47(7) : 653.

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