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7,9-bis(benzyloxy)-3-hydroxy-1-methyl-6H-benzo[c]chromen-6-one

中文名称
——
中文别名
——
英文名称
7,9-bis(benzyloxy)-3-hydroxy-1-methyl-6H-benzo[c]chromen-6-one
英文别名
alternariol-7,9-dibenzyl ether;ADBE;3-Hydroxy-1-methyl-7,9-bis(phenylmethoxy)benzo[c]chromen-6-one;3-hydroxy-1-methyl-7,9-bis(phenylmethoxy)benzo[c]chromen-6-one
7,9-bis(benzyloxy)-3-hydroxy-1-methyl-6H-benzo[c]chromen-6-one化学式
CAS
——
化学式
C28H22O5
mdl
——
分子量
438.48
InChiKey
XORDHQYSNDXMKG-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6
  • 重原子数:
    33
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    65
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    7,9-bis(benzyloxy)-3-hydroxy-1-methyl-6H-benzo[c]chromen-6-one1,2-二甲基咪唑 、 palladium 10% on activated carbon 、 甲酸铵 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 17.0h, 生成
    参考文献:
    名称:
    Total synthesis of masked Alternaria mycotoxins—sulfates and glucosides of alternariol (AOH) and alternariol-9-methyl ether (AME)
    摘要:
    The synthesis of different protected alternariol derivatives using intramolecular cyclization of iodoresorcylic acid phenyl esters by palladium-catalyzed C-H activation as key step is presented. Furthermore, chemical sulfation and glucosylation were applied for the preparation of conjugated Alternaria mycotoxins. These compounds are suspected to be formed during metabolism in contaminated plants. Therefore, all synthetic conjugates prepared within this work serve as reference materials for further studies in the fields of bioanalytics and toxicology of mycotoxins. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2013.10.008
  • 作为产物:
    描述:
    3,5-二甲氧基碘苯4-二甲氨基吡啶sodium chloritesodium dihydrogenphosphate dihydrate2-甲基-2-丁烯 、 palladium diacetate 、 三溴化磷 、 sodium hydride 、 potassium carbonate盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺三氯氧磷 作用下, 以 四氢呋喃二氯甲烷N,N-二甲基乙酰胺乙腈叔丁醇 为溶剂, 反应 36.75h, 生成 7,9-bis(benzyloxy)-3-hydroxy-1-methyl-6H-benzo[c]chromen-6-one 、 7,9-bis(benzyloxy)-1-hydroxy-3-methyl-6H-benzo[c]chromen-6-one
    参考文献:
    名称:
    Total synthesis of masked Alternaria mycotoxins—sulfates and glucosides of alternariol (AOH) and alternariol-9-methyl ether (AME)
    摘要:
    The synthesis of different protected alternariol derivatives using intramolecular cyclization of iodoresorcylic acid phenyl esters by palladium-catalyzed C-H activation as key step is presented. Furthermore, chemical sulfation and glucosylation were applied for the preparation of conjugated Alternaria mycotoxins. These compounds are suspected to be formed during metabolism in contaminated plants. Therefore, all synthetic conjugates prepared within this work serve as reference materials for further studies in the fields of bioanalytics and toxicology of mycotoxins. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2013.10.008
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文献信息

  • Total synthesis of masked Alternaria mycotoxins—sulfates and glucosides of alternariol (AOH) and alternariol-9-methyl ether (AME)
    作者:Hannes Mikula、Philipp Skrinjar、Barbara Sohr、Doris Ellmer、Christian Hametner、Johannes Fröhlich
    DOI:10.1016/j.tet.2013.10.008
    日期:2013.12
    The synthesis of different protected alternariol derivatives using intramolecular cyclization of iodoresorcylic acid phenyl esters by palladium-catalyzed C-H activation as key step is presented. Furthermore, chemical sulfation and glucosylation were applied for the preparation of conjugated Alternaria mycotoxins. These compounds are suspected to be formed during metabolism in contaminated plants. Therefore, all synthetic conjugates prepared within this work serve as reference materials for further studies in the fields of bioanalytics and toxicology of mycotoxins. (C) 2013 Elsevier Ltd. All rights reserved.
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