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(1S,5S,6R)-(cis,trans)-spiro[4.4]nonane-1,6-diol | 65167-79-5

中文名称
——
中文别名
——
英文名称
(1S,5S,6R)-(cis,trans)-spiro[4.4]nonane-1,6-diol
英文别名
——
(1S,5S,6R)-(cis,trans)-spiro[4.4]nonane-1,6-diol化学式
CAS
65167-79-5
化学式
C9H16O2
mdl
——
分子量
156.225
InChiKey
ACIVJWAOSTYYEP-YIZRAAEISA-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):
    1.06
  • 重原子数:
    11.0
  • 可旋转键数:
    0.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    40.46
  • 氢给体数:
    2.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    三氟甲磺酸酐(1S,5S,6R)-(cis,trans)-spiro[4.4]nonane-1,6-diol三乙胺 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 生成 Trifluoro-methanesulfonic acid (1S,5S,6R)-6-trifluoromethanesulfonyloxy-spiro[4.4]non-1-yl ester
    参考文献:
    名称:
    手性恶唑硼烷催化的高效和立体定向硼烷还原螺[4,4]壬烷-1,6-二酮
    摘要:
    描述了由恶唑硼烷试剂催化的高度立体选择性和对映选择性还原外消旋螺[4,4]壬烷-1,6-二酮。外消旋螺二酮的不对称还原产生对映体纯的螺二醇,其是有用的手性助剂,也是合成其他高效手性配体的关键中间体。的反式,反式-和顺式,反式均在高对映体纯度通过手性采用恶唑硼烷作为催化剂制备-spirodiols。
    DOI:
    10.1016/s0040-4039(00)00606-7
  • 作为产物:
    描述:
    (+/-)-trans-6-hydroxyspiro<4.4>nonan-1-one 为溶剂, 反应 72.0h, 生成 (1S,5S,6R)-(cis,trans)-spiro[4.4]nonane-1,6-diol 、 trans,trans-spiro<4.4>nonane-1,6-diol
    参考文献:
    名称:
    Microbial stereodifferentiating reduction of 1,6-spiro[4.4]nonanedione, a gyrochiral diketone with two homotopic carbonyl groups
    摘要:
    DOI:
    10.1021/jo00319a021
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文献信息

  • Asymmetric synthesis. Part 29: Asymmetric hydroformylation of styrene catalyzed by chiral spiro diphosphite–rhodium(I) complexes
    作者:Yaozhong Jiang、Song Xue、Zhi Li、Jingen Deng、Aiqiao Mi、Albert S.C. Chan
    DOI:10.1016/s0957-4166(98)00339-5
    日期:1998.9
    Chiral diphosphite ligands L1–L3 were prepared by the reaction of (1S,5S,6R)-(cis,trans)-spiro[4.4]nonane-1,6-diol with chlorophosphites. These ligands were tested in the rhodium catalyzed hydroformylation of styrene and enantioselectivities up to 69% were achieved. High regioselectivities (97%) to 2-phenylpropanal and high yields (98%) were obtained under mild reaction conditions. The influence of
    通过(1 S,5 S,6 R)-(顺式,反式)-螺[4.4]壬烷-1,6-二醇亚磷酸酯的反应制备手性二亚磷酸配体L 1 -L 3。在催化的苯乙烯的加氢甲酰化反应中测试了这些配体,对映选择性高达69%。在温和的反应条件下,对2-苯基丙醛的区域选择性高(97%),产率高(98%)。还讨论了反应条件的影响。
  • PLATINUM COMPLEX AND MEDICAL COMPOUND CONTAINING SAME
    申请人:Unitech Co., Ltd
    公开号:EP2325163A1
    公开(公告)日:2011-05-25
    A new platinum complex which has strong antitumor activity and has effect with smaller doses and a pharmaceutical composition containing the same are provided. A spiro[4,4]nonme-1,6-diamineplatinum(II) complex which is represented by a following general formula (A). (In the formula, X and Y are same or different, and X and Y represent halogen atoms respectively, or X and Y cooperatively represent a divalent residue which is described by a formula (Z) .) The platinum complex has a strong antitumor activity and is efficacious as a therapeutic agent for malignant tumors.
    本研究提供了一种抗肿瘤活性强、剂量较小的新型络合物和含有该络合物的药物组合物。一种螺[4,4]壬-1,6-二(II)络合物,由以下通式(A)表示。(式中,X 和 Y 相同或不同,X 和 Y 分别代表卤素原子,或 X 和 Y 共同代表二价残基,二价残基用式(Z)表示)。络合物具有很强的抗肿瘤活性,可作为恶性肿瘤的有效治疗剂。
  • PLATINUM COMPLEX AND PHARMACEUTICAL COMPOSITION CONTAINING THE SAME
    申请人:Arai Hisae
    公开号:US20110152555A1
    公开(公告)日:2011-06-23
    A new platinum complex which has strong antitumor activity and has effect with smaller doses and a pharmaceutical composition containing the same are provided. A spiro[4,4]nonane-1,6-diamineplatinum(II) complex which is represented by a following general formula (A). (In the formula, X and Y are same or different, and X and Y represent halogen atoms respectively, or X and Y cooperatively represent a divalent residue which is described by a formula (Z).) The platinum complex has a strong antitumor activity and is efficacious as a therapeutic agent for malignant tumors.
  • US8501977B2
    申请人:——
    公开号:US8501977B2
    公开(公告)日:2013-08-06
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