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rel-(2R,3R)-2-methyl-1,3-(isopropylidenedioxy)nonane | 137920-18-4

中文名称
——
中文别名
——
英文名称
rel-(2R,3R)-2-methyl-1,3-(isopropylidenedioxy)nonane
英文别名
4-hexyl-2,2,5-trimethyl-[1,3]dioxane;(4R,5R)-4-hexyl-2,2,5-trimethyl-1,3-dioxane
rel-(2R,3R)-2-methyl-1,3-(isopropylidenedioxy)nonane化学式
CAS
137920-18-4
化学式
C13H26O2
mdl
——
分子量
214.348
InChiKey
XCPZNJSVOPOVSS-VXGBXAGGSA-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):
    4.2
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    rel-(7R,8R)-7<(methoxymethyl)oxy>-8-methyl-9-heptadecyne 在 Lindlar's catalyst 盐酸 、 sodium tetrahydroborate 、 二甲基硫氢气4-甲基苯磺酸吡啶臭氧 作用下, 以 甲醇 为溶剂, 反应 4.34h, 生成 rel-(2R,3R)-2-methyl-1,3-(isopropylidenedioxy)nonane
    参考文献:
    名称:
    Synthesis of enantioenriched homopropargylic alcohols through diastereoselective SE' additions of chiral allenylstannanes to aldehydes
    摘要:
    Allenylstannanes (S)-4 and (R)-4, available in ca. 90% ee from alkynones 1 through reduction with the LiAlH4-Darvon alcohol or -ent-Darvon alcohol complex, followed by S(N)2' displacement on the derived mesylates (R)-3 or (S)-3 with Bu3SnLi.CuBr.Me2S, readily add to various aldehydes under Lewis acid catalysis to afford optically active homopropargylic alcohols with good to excellent syn diastereoselectivity. With 2-(benzyloxy)propanal (48), MgBr2-catalyzed reactions are highly stereoselective, affording the syn adduct 49 from the (S)-stannane (S)-4 and the anti adduct 52 from the (R)-stannane (R)-4. BF3-promoted additions give mainly or exclusively the syn adducts 49 and 51. Additions of (S)- and (R)-4 to (R)-3-(benzyloxy)-2-methylpropanal (61) yield the syn adducts 62 and 64 as major or exclusive products.
    DOI:
    10.1021/jo00030a036
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文献信息

  • Surprising Role of Aryl Halides in Nickel-Catalyzed Reductive Aldol Reactions
    作者:Christa C. Chrovian、John Montgomery
    DOI:10.1021/ol063028+
    日期:2007.2.1
    [reaction: see text] A new nickel-catalyzed method for the reductive aldol addition of acrylates and aldehydes has been developed. An unexpected requirement for an aryl iodide additive was found in the process, and the effect was shown to be linked to an initiation step.
    [反应:见正文]已经开发了一种新的催化的丙烯酸酯和醛的醛醇缩合加成方法。在该方法中发现了对芳基化物添加剂的出乎意料的要求,并且显示出该效果与引发步骤有关。
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