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3-[(2S,3R,4R,5S,6S)-2-bromomethyl-5-(tert-butyldimethylsilyloxy)-6-methoxy-3-pivaloyloxymethyltetrahydropyran-4-yl]propyl pivalate | 1030028-02-4

中文名称
——
中文别名
——
英文名称
3-[(2S,3R,4R,5S,6S)-2-bromomethyl-5-(tert-butyldimethylsilyloxy)-6-methoxy-3-pivaloyloxymethyltetrahydropyran-4-yl]propyl pivalate
英文别名
——
3-[(2S,3R,4R,5S,6S)-2-bromomethyl-5-(tert-butyldimethylsilyloxy)-6-methoxy-3-pivaloyloxymethyltetrahydropyran-4-yl]propyl pivalate化学式
CAS
1030028-02-4
化学式
C27H51BrO7Si
mdl
——
分子量
595.687
InChiKey
BAETVAFKTJXBHN-TWGBQZSLSA-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

反应信息

  • 作为反应物:
    描述:
    3-[(2S,3R,4R,5S,6S)-2-bromomethyl-5-(tert-butyldimethylsilyloxy)-6-methoxy-3-pivaloyloxymethyltetrahydropyran-4-yl]propyl pivalate 在 sodium cyanoborohydride 、 作用下, 以 丙醇 为溶剂, 以100%的产率得到(4R,5R)-4-[(S)-1-(tert-butyldimethylsilyloxy)-2-hydroxyethyl]-5-(pivaloyloxymethyl)-hept-6-enyl pivalate
    参考文献:
    名称:
    The 2α-(3-hydroxypropyl) group as an active motif in vitamin D3 analogues as agonists of the mutant vitamin D receptor (Arg274Leu)
    摘要:
    We designed and synthesized 1 alpha- and 1 beta-hydroxymethyl-2 alpha-(3-hydroxypropyl)-25-hydroxyvitamin D-3 (2a,b) and related analogues 2 alpha-(3-hydroxypropyl)-25-hydroxyvitamin D-3 (3), Posner's analogues of 1 alpha- and 1 beta-hydroxymethyl-25-hydroxyvitamin D-3 (4a,b), as well as 2 alpha-(3-hydroxypropyl)-1 alpha,25-dihydroxyvitamin D-3 (5), to confirm the effect of the 1 alpha-hydroxy group and/or 2 alpha-(3-hydroxypropyl) group of vitamin D-3 analogues with the modified A-ring moiety on the mutant vitamin D receptor, VDR(Arg274Leu). The 2 alpha-(3-hydroxypropyl) group showed better effect on enhancement of the transcriptional activity through the mutant VDR than the 1 alpha- and 1 beta-hydroxymethyl groups. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.12.039
  • 作为产物:
    描述:
    3-[(2S,3R,4R,5S,6S)-5-(tert-butyldimethylsilyloxy)-2-methanesulfonyloxymethyl-6-methoxy-3-pivaloyloxymethyltetrahydropyran-4-yl]propyl pivalate 在 lithium bromide 作用下, 以 various solvent(s) 为溶剂, 以78%的产率得到3-[(2S,3R,4R,5S,6S)-2-bromomethyl-5-(tert-butyldimethylsilyloxy)-6-methoxy-3-pivaloyloxymethyltetrahydropyran-4-yl]propyl pivalate
    参考文献:
    名称:
    The 2α-(3-hydroxypropyl) group as an active motif in vitamin D3 analogues as agonists of the mutant vitamin D receptor (Arg274Leu)
    摘要:
    We designed and synthesized 1 alpha- and 1 beta-hydroxymethyl-2 alpha-(3-hydroxypropyl)-25-hydroxyvitamin D-3 (2a,b) and related analogues 2 alpha-(3-hydroxypropyl)-25-hydroxyvitamin D-3 (3), Posner's analogues of 1 alpha- and 1 beta-hydroxymethyl-25-hydroxyvitamin D-3 (4a,b), as well as 2 alpha-(3-hydroxypropyl)-1 alpha,25-dihydroxyvitamin D-3 (5), to confirm the effect of the 1 alpha-hydroxy group and/or 2 alpha-(3-hydroxypropyl) group of vitamin D-3 analogues with the modified A-ring moiety on the mutant vitamin D receptor, VDR(Arg274Leu). The 2 alpha-(3-hydroxypropyl) group showed better effect on enhancement of the transcriptional activity through the mutant VDR than the 1 alpha- and 1 beta-hydroxymethyl groups. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.12.039
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