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(2S,4S,5R)-2-(4-Methoxy-phenyl)-5-methyl-[1,3]dioxane-4-carbaldehyde | 501084-30-6

中文名称
——
中文别名
——
英文名称
(2S,4S,5R)-2-(4-Methoxy-phenyl)-5-methyl-[1,3]dioxane-4-carbaldehyde
英文别名
(2S,4S,5R)-2-(4-methoxyphenyl)-5-methyl-1,3-dioxane-4-carbaldehyde
(2S,4S,5R)-2-(4-Methoxy-phenyl)-5-methyl-[1,3]dioxane-4-carbaldehyde化学式
CAS
501084-30-6
化学式
C13H16O4
mdl
——
分子量
236.268
InChiKey
MNQAPGBMXMPHSL-WQAKAFBOSA-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):
    1.7
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (2S,4S,5R)-2-(4-Methoxy-phenyl)-5-methyl-[1,3]dioxane-4-carbaldehyde正丁基锂N-甲基吲哚酮 、 四丙基高钌酸铵 、 4 A molecular sieve 、 二异丙胺 作用下, 以 四氢呋喃乙醚二氯甲烷 为溶剂, 反应 3.25h, 生成 (2S,3S)-3-Hydroxy-3-[(2R,4R,5S)-2-(4-methoxy-phenyl)-5-methyl-[1,3]dioxan-4-yl]-1-[(2S,4S,5R)-2-(4-methoxy-phenyl)-5-methyl-[1,3]dioxan-4-yl]-2-methyl-propan-1-one
    参考文献:
    名称:
    Synthesis and Conformational Analysis of meso-Ter(1,3-dioxan-4-yls)
    摘要:
    A convergent synthesis of the meso-ter(1,3-dioxanyls) 8-11 has been achieved, starting from two enantiomeric building blocks in each case. The stereogenic centres in the central linkage region were set up by stereocontrolled aldol additions. Structure assignment of the final products was based on comparisons between experimental and calculated (3)J(H,H) coupling constants, which reflect distinct conformer populations. (C) Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.
    DOI:
    10.1002/1099-0690(200210)2002:20<3455::aid-ejoc3455>3.0.co;2-v
  • 作为产物:
    描述:
    4-甲氧基苯甲醛二乙基缩醛 在 camphor-10-sulfonic acid 四丁基氟化铵戴斯-马丁氧化剂 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 40.0 ℃ 、1.5 kPa 条件下, 反应 4.83h, 生成 (2S,4S,5R)-2-(4-Methoxy-phenyl)-5-methyl-[1,3]dioxane-4-carbaldehyde
    参考文献:
    名称:
    Synthesis and Conformational Analysis of meso-Ter(1,3-dioxan-4-yls)
    摘要:
    A convergent synthesis of the meso-ter(1,3-dioxanyls) 8-11 has been achieved, starting from two enantiomeric building blocks in each case. The stereogenic centres in the central linkage region were set up by stereocontrolled aldol additions. Structure assignment of the final products was based on comparisons between experimental and calculated (3)J(H,H) coupling constants, which reflect distinct conformer populations. (C) Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.
    DOI:
    10.1002/1099-0690(200210)2002:20<3455::aid-ejoc3455>3.0.co;2-v
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文献信息

  • γ-Allyl Phosphinoyl Phenyl Sulfone (GAPPS):  A Conjunctive Reagent for the Synthesis of EE, EZ, and ET 1,3-Dienes
    作者:Xiaojin Li、Douglas Lantrip、Philip L. Fuchs
    DOI:10.1021/ja0377596
    日期:2003.11.1
    A three-operation conjunctive strategy is available for the synthesis of EE, EZ, and ET dienes. This protocol employs a sequential Wadsworth-Emmons reaction using a GAPPS reagent followed by alkylation of an allylic sulfone anion, and finally ligand-mediated, palladium-catalyzed desulfonylation.
  • Synthesis and Conformational Analysis of meso-Ter(1,3-dioxan-4-yls)
    作者:Reinhard W. Hoffmann、Gemma Mas、Trixi Brandl
    DOI:10.1002/1099-0690(200210)2002:20<3455::aid-ejoc3455>3.0.co;2-v
    日期:2002.10
    A convergent synthesis of the meso-ter(1,3-dioxanyls) 8-11 has been achieved, starting from two enantiomeric building blocks in each case. The stereogenic centres in the central linkage region were set up by stereocontrolled aldol additions. Structure assignment of the final products was based on comparisons between experimental and calculated (3)J(H,H) coupling constants, which reflect distinct conformer populations. (C) Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.
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