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3-amino-3-deoxyα-D-glucopyranosyl-(1→1')-3'-amino-3'-deoxy-α-D-glucopyranoside | 771424-03-4

中文名称
——
中文别名
——
英文名称
3-amino-3-deoxyα-D-glucopyranosyl-(1→1')-3'-amino-3'-deoxy-α-D-glucopyranoside
英文别名
(2R,3R,4S,5S,6R)-4-amino-2-[(2R,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-(hydroxymethyl)oxane-3,5-diol
3-amino-3-deoxyα-D-glucopyranosyl-(1→1')-3'-amino-3'-deoxy-α-D-glucopyranoside化学式
CAS
771424-03-4
化学式
C12H24N2O9
mdl
——
分子量
340.331
InChiKey
ZPEFXARQZVAHGO-LJXPPPJUSA-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:
    23
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    201
  • 氢给体数:
    8
  • 氢受体数:
    11

反应信息

  • 作为产物:
    描述:
    6-O-acetyl-3-azido-2,4-di-O-benzyl-3-deoxy-a-D-glucopyranosyl-(1→1')-6-O-acetyl-3'-azido-2',4'-di-O-benzyl-3'-deoxy-a-D-glucopyranoside 在 sodium 、 palladium(II) hydroxide 、 作用下, 以 甲醇 为溶剂, 反应 40.08h, 生成 3-amino-3-deoxyα-D-glucopyranosyl-(1→1')-3'-amino-3'-deoxy-α-D-glucopyranoside
    参考文献:
    名称:
    Synthesis of 3,3′-neotrehalosadiamine and related 1,1′-aminodisaccharides using disarmed, armed, and superarmed building blocks
    摘要:
    Here we report a high yielding, stereoselective synthesis of the naturally occurring 1,1'-disaccharide neotrehalosadiamine (NTD) and some related analogs. Following an eleven-step sequence, seven of which did not require chromatographic separation, NTD was generated in 60% overall yield from the inexpensive, commercially available precursor 1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranose. The key alpha,beta-linkage of NTD was formed in a highly stereoselective manner by taking advantage of the participating effect of the acyl group at O-2 of the donor glycoside. The influence of electronic effects of disarmed, armed, and superarmed glycosyl donors and acceptors on the outcome of 1,1'-glycosidation was also observed. Antibacterial studies using NTD and its analogs show detectable but weak antistaphylococcal activity. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.10.058
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