摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(2S,3R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentane-1,3-diol | 1242057-45-9

中文名称
——
中文别名
——
英文名称
(2S,3R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentane-1,3-diol
英文别名
——
(2S,3R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentane-1,3-diol化学式
CAS
1242057-45-9
化学式
C15H30O4
mdl
——
分子量
274.401
InChiKey
CYDMLPZPGNFWPE-GMDXDWKASA-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):
    2.5
  • 重原子数:
    19
  • 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:
    58.9
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    (2S,3R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentane-1,3-diol叔丁基二甲基氯硅烷咪唑 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以90%的产率得到(2S,3R,4R)-1-((tert-butyldimethylsilyl)oxy)-4-((4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl)-2-methylpentan-3-ol
    参考文献:
    名称:
    Synthesis of C15–C27 segment of venturicidine X by utilizing desymmetrization protocol
    摘要:
    We have achieved the synthesis of C15-C27 fragment of venturicidine X using desymmetrization protocol, substrate-controlled Grignard reaction, Barton-McCombie reaction, Sharpless epoxidation, and TBSOTf-mediated rearrangement to produce the aldol product through a non-aldol route as the key step following 23 longest linear sequences with 6.4% overall yield starting from a known intermediate 11. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.05.148
  • 作为产物:
    描述:
    在 palladium 10% on activated carbon 、 氢气 作用下, 以 正己烷 为溶剂, 反应 12.0h, 以89%的产率得到(2S,3R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentane-1,3-diol
    参考文献:
    名称:
    Synthesis of C15–C27 segment of venturicidine X by utilizing desymmetrization protocol
    摘要:
    We have achieved the synthesis of C15-C27 fragment of venturicidine X using desymmetrization protocol, substrate-controlled Grignard reaction, Barton-McCombie reaction, Sharpless epoxidation, and TBSOTf-mediated rearrangement to produce the aldol product through a non-aldol route as the key step following 23 longest linear sequences with 6.4% overall yield starting from a known intermediate 11. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.05.148
点击查看最新优质反应信息

文献信息

  • Synthesis of C15–C27 segment of venturicidine X by utilizing desymmetrization protocol
    作者:J.S. Yadav、Sk. Samad Hossain、Debendra K. Mohapatra
    DOI:10.1016/j.tetlet.2010.05.148
    日期:2010.8
    We have achieved the synthesis of C15-C27 fragment of venturicidine X using desymmetrization protocol, substrate-controlled Grignard reaction, Barton-McCombie reaction, Sharpless epoxidation, and TBSOTf-mediated rearrangement to produce the aldol product through a non-aldol route as the key step following 23 longest linear sequences with 6.4% overall yield starting from a known intermediate 11. (C) 2010 Elsevier Ltd. All rights reserved.
查看更多