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methyl 2,3,4-tri-O-acetyl-6-deoxy-β-D-glucopyranoside | 6340-57-4

中文名称
——
中文别名
——
英文名称
methyl 2,3,4-tri-O-acetyl-6-deoxy-β-D-glucopyranoside
英文别名
1(β)-O-Methyl-2,3,4-triacetyl-6-deoxy-glucose;methyl β-D-quinovopyranoside acetate;methyl-(tri-O-acetyl-6-deoxy-β-D-glucopyranoside);Methyl-(tri-O-acetyl-6-desoxy-β-D-glucopyranosid);[(2R,3R,4S,5R,6R)-4,5-diacetyloxy-6-methoxy-2-methyloxan-3-yl] acetate
methyl 2,3,4-tri-O-acetyl-6-deoxy-β-D-glucopyranoside化学式
CAS
6340-57-4
化学式
C13H20O8
mdl
——
分子量
304.297
InChiKey
RTVWBDNQHISFHI-HVWSPFAKSA-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):
    0.2
  • 重原子数:
    21
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.77
  • 拓扑面积:
    97.4
  • 氢给体数:
    0
  • 氢受体数:
    8

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

点击查看最新优质反应信息

文献信息

  • A convenient and general synthesis of 5-vinylhexofuranosides from 6-halo-6-deoxypyranosides
    作者:Masami Nakane、C. Richard Hutchinson、Harold Gollman
    DOI:10.1016/s0040-4039(00)71373-6
    日期:——
    The synthesis of five different 5,6-dideoxyhex-5-enofuranosides (5, 7, 9 and 11) proceeds in 30–60% overall yield in two steps from commercially available 1-0-methyl pyranosides by reductive β-elimination of the intermediate 6-bromo-6-deoxypyranosides.
    通过还原性的β-消除作用,从市售的1-0-甲基吡喃糖苷中分两步合成了5种不同的5,6-二脱氧己基-5-烯呋喃糖苷(5、7、9和11),总产率为30-60%。中间体6-溴-6-脱氧吡喃糖苷。
  • The structure of a novel nucleoside antibiotic, dapiramicin A
    作者:Haruo Seto、Noburu Otake、Masao Koyama、Hiroko Ogino、Yoshio Kodama、Nobusuke Nishizawa、Takashi Tsuruoka、Shigeharu Inouye
    DOI:10.1016/s0040-4039(00)81446-x
    日期:——
    Based on 1H- and 13C-NMR spectral data including deuterium induced upfield shift, the structure of dapiramicin A, a novel nucleoside antibiotic has been determined as shown in Fig. 5.
    根据1 H和13 C-NMR光谱数据,包括氘诱导的高场位移,确定了一种新型核苷抗生素dapiramicin A的结构,如图5所示。
  • The Dimolar Tosylation of β-Methylcellobioside: α-Cellobiomethylose
    作者:Jack Compton
    DOI:10.1021/ja01272a059
    日期:1938.5
  • A One-Pot Method for Removal of Thioacetyl Group via Desulfurization under Ultraviolet Light To Synthesize Deoxyglycosides
    作者:Jian-Tao Ge、Lang Zhou、Tao Luo、Jian Lv、Hai Dong
    DOI:10.1021/acs.orglett.9b02033
    日期:2019.8.2
    We herein developed an efficient method for removing thioacetyl to synthesize acylated deoxy glycosides in a one-pot reaction, where the thioacetyl was selectively deacetylated by hydrazine hydrate in DMF within 2-5 min at room temperature, followed by desulfurization under UV light for 1-2 h in the presence of TCEP center dot HCl. The method was then used to synthesize 2-deoxy glycosides with absolute alpha/beta-configuration via stereoselective control of C-2 thioacetate in glycosylation.
  • The Unimolar Tosylation<sup>1</sup> of alpha- and beta-Methyl-d-glucosides
    作者:Jack Compton
    DOI:10.1021/ja01269a045
    日期:1938.2
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