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Phebaclavin C的全合成研究
  • ISSN号：0253-2786
  • 期刊名称：《有机化学》
  • 时间：0
  • 分类：O62[理学—有机化学;理学—化学]
  • 作者机构：[1]兰州大学化学化工学院,功能有机分子化学国家重点实验室,兰州,730000 兰州大学化学化工学院,功能有机分子化学国家重点实验室,兰州,730000 兰州大学化学化工学院,功能有机分子化学国家重点实验室,兰州,730000
  • 相关基金：国家自然科学基金(群体基金No.20021001)资助项目.
作者： 张宇[1], 刘冬[1], 曹小平[1]
中文摘要：

　　天然存在的香豆素类化合物具有良好的生理活性和光学活性[1].PhebaclavinA～H是2002年Muyard等从分布于澳大利亚东南部和新西兰北部的植物Phebalium clavatum中分离出来的八个3位具有异戊烯基结构的天然产物[2],其合成尚未见文献报道.我们小组在对香豆素合成研究的基础上,以2,4-二羟基苯甲醛为原料,高温关环、末端双键氧化成醛等为关键步骤,高产率、高立体选择性地合成了Phebaclavin C(1),从而探索出一条简便、实用的合成该类化合物的通用方法.1的谱图数据与文献报道一致,其它化合物的合成正在进行之中.……

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期刊信息
  • 《有机化学》
  • 中国科技核心期刊
  • 主管单位:
  • 主办单位:中国化学会 中国科学院上海有机化学研究所
  • 主编：陈庆云
  • 地址：上海市枫林路354号
  • 邮编：200032
  • 邮箱：bianji@mail.sioc.ac.cn
  • 电话：021-54925244
  • 国际标准刊号：ISSN：0253-2786
  • 国内统一刊号：ISSN：31-1321/O6
  • 邮发代号:4-285
  • 获奖情况:
  • 中国期刊方阵“双效”期刊
  • 国内外数据库收录:
  • 俄罗斯文摘杂志,美国化学文摘（网络版）,荷兰文摘与引文数据库,美国科学引文索引（扩展库）,日本日本科学技术振兴机构数据库,中国中国科技核心期刊,中国北大核心期刊（2004版）,中国北大核心期刊（2008版）,中国北大核心期刊（2011版）,中国北大核心期刊（2014版）,中国北大核心期刊（2000版）
  • 被引量:14408