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dimethyl (benzyl 2,3,4-tri-O-benzyl-α-D-manno-heptopyranos-6-ulos-7-yl)phosphonate | 222417-79-0

中文名称
——
中文别名
——
英文名称
dimethyl (benzyl 2,3,4-tri-O-benzyl-α-D-manno-heptopyranos-6-ulos-7-yl)phosphonate
英文别名
2-[dimethoxy(oxido)phosphaniumyl]-1-[(2S,3S,4S,5S,6S)-3,4,5,6-tetrakis(phenylmethoxy)oxan-2-yl]ethanone
dimethyl (benzyl 2,3,4-tri-O-benzyl-α-D-manno-heptopyranos-6-ulos-7-yl)phosphonate化学式
CAS
222417-79-0
化学式
C37H41O9P
mdl
——
分子量
660.701
InChiKey
DPMSORJUKBRMCT-DWCHZDDLSA-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):
    4.7
  • 重原子数:
    47
  • 可旋转键数:
    17
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    105
  • 氢给体数:
    0
  • 氢受体数:
    9

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Synthesis of Sugar-Derived 2′- and 3′-Substituted Furans and Their Application in Diels−Alder Reactions
    作者:Sławomir Jarosz、Mateusz Mach、Katarzyna Szewczyk、Stanisław Skóra、Zbigniew Ciunik
    DOI:10.1002/1099-0690(200108)2001:15<2955::aid-ejoc2955>3.0.co;2-0
    日期:2001.8
    A convenient synthesis of 2′- and 3′-furyl sugars in which the furan and the sugar parts are directly connected is presented. The key step comprises HF·py-induced cyclization of α,β-unsaturated carbonyl compounds (ketones or aldehydes) possessing terminal hydroxymethylene groups protected as TBDPS ethers. Treatment of such furan derivatives with N-phenylmaleimide under high-pressure conditions (11
    提出了一种2'-和3'-呋喃糖的便捷合成方法,其中呋喃和糖部分直接相连。关键步骤包括HF·py诱导的具有被保护为TBDPS醚的末端羟基亚甲基的α,β-不饱和羰基化合物(酮或醛)的环化反应。在高压条件下(11 kbar)用N-苯基马来酰亚胺处理此类呋喃生物可生成相应的[4 + 2]加合物,其中内型占主导。然而,在p = 1 atm和T = 20°C时,形成了exo异构体作为主要产物。[4 + 2]加合物在升高的温度和大气压下进行逆狄尔斯-阿尔德反应。
  • A convenient route to enantiomerically pure bicyclo[4.3.0]nonanes from sugar allyltin derivatives
    作者:Sławomir Jarosz、Stanisław Skóra
    DOI:10.1016/s0957-4166(00)00083-5
    日期:2000.4
    Tandem Wittig-type Diels-Alder reactions between sugar derived phosphonates and dienoaldehydes obtained from sugar allyltins lead, with high stereoselectivity, to complex oxygenated perhydroindene derivatives with the trans junction between the five- and six-membered rings. The configuration at the newly created stereogenic centers in such bicyclo[4.3.0] systems may be monitored by the geometry of chiral phosphonates. (C) 2000 Elsevier Science Ltd. All rights reserved.
  • REACTION OF SUGAR PHOSPHONATES WITH SUCROSE ALDEHYDES. SYNTHESIS OF HIGHER ANALOGS OF SUCROSE
    作者:Mateusz Mach、Sławomir Jarosz
    DOI:10.1081/car-100105713
    日期:2001.6.30
    The Horner-Emmons reaction between sugar phosphonates Sug-C(O)CH2 P(O)(OMe)(2) and aldehydes derived from sucrose afforded precursors of higher analogs of the general formula Sug-C(O)CH==CH-Suc. An example of the functionalization of the internal three-carbon saccharide connecting unit is provided.
  • Convenient approach to higher carbon sugars. First synthesis of the free C12-sugar: d-erythro-l-manno-d-manno-dodecose
    作者:Sławomir Jarosz、Stanisław Skóra、Izabela Kościołowska
    DOI:10.1016/s0008-6215(02)00484-6
    日期:2003.2
    The model synthesis of a C12-aldose was initiated from the easily available dimethyl(benzyl 2,3,4-tri-O-benzyl-alpha-D-manno-heptopyranos-6-ulos-7-yl)phosphonate and 2,3:4,5-di-O-isopropylidene-D-arabinose. (C) 2003 Published by Elsevier Science Ltd.
  • Jarosz, Sławomir; Mach, Mateusz; Skóra, Staniław, Synlett, 1999, # 3, p. 313 - 314
    作者:Jarosz, Sławomir、Mach, Mateusz、Skóra, Staniław
    DOI:——
    日期:——
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