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

2,3,4-tri-O-benzyl-6-O-tert-butyldimethylsilyl-D-altrono-1,5-lactone | 948036-10-0

中文名称
——
中文别名
——
英文名称
2,3,4-tri-O-benzyl-6-O-tert-butyldimethylsilyl-D-altrono-1,5-lactone
英文别名
(3S,4R,5R,6R)-6-[(tert-butyldimethylsilyl)oxy]methyl-3,4,5-trisbenzyloxy-tetrahydropyran-2-one;(3S,4R,5R,6R)-6-[[tert-butyl(dimethyl)silyl]oxymethyl]-3,4,5-tris(phenylmethoxy)oxan-2-one
2,3,4-tri-O-benzyl-6-O-tert-butyldimethylsilyl-D-altrono-1,5-lactone化学式
CAS
948036-10-0
化学式
C33H42O6Si
mdl
——
分子量
562.778
InChiKey
QOBGJUJDMVPGLT-VTMRUAGOSA-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):
    6.69
  • 重原子数:
    40
  • 可旋转键数:
    13
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    63.2
  • 氢给体数:
    0
  • 氢受体数:
    6

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

  • 作为反应物:
    描述:
    2,3,4-tri-O-benzyl-6-O-tert-butyldimethylsilyl-D-altrono-1,5-lactonecalcium sulfate 、 cerium(III) chloride 、 三氟甲磺酸 作用下, 以 甲苯乙腈 为溶剂, 反应 3.0h, 生成 (1R,2R,3R,4S,5R)-2,3,4-tris(benzyloxy)-5-vinyl-6,8-dioxabicyclo[3.2.1]octane
    参考文献:
    名称:
    Synthesis of a partially benzylated derivative of the anhydro-d-altro-heptulose found in Coriaria japonica A
    摘要:
    A partially benzylated derivative of the anhydro-D-altro-heptulose found in Coriaria japonica A, which is a synthetically useful unit, was successfully synthesized from a D-mannose derivative by a novel synthetic approach involving an intramolecular O-ketopyranosylation. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.06.057
  • 作为产物:
    描述:
    叔丁基二甲基氯硅烷 在 palladium dichloride 吡啶咪唑18-冠醚-6sodium methylate 、 sodium hydride 作用下, 以 甲醇二氯甲烷 、 acetate buffer 、 N,N-二甲基甲酰胺甲苯 为溶剂, 反应 32.5h, 生成 2,3,4-tri-O-benzyl-6-O-tert-butyldimethylsilyl-D-altrono-1,5-lactone
    参考文献:
    名称:
    Synthesis of a partially benzylated derivative of the anhydro-d-altro-heptulose found in Coriaria japonica A
    摘要:
    A partially benzylated derivative of the anhydro-D-altro-heptulose found in Coriaria japonica A, which is a synthetically useful unit, was successfully synthesized from a D-mannose derivative by a novel synthetic approach involving an intramolecular O-ketopyranosylation. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.06.057
点击查看最新优质反应信息

文献信息

  • Syntheses of a partially benzylated derivative of the anhydro-d-altro-heptulose found in Coriaria japonica A and of its analogs
    作者:Sho Matsuda、Takashi Yamanoi、Mikio Watanabe
    DOI:10.1016/j.tet.2008.06.068
    日期:2008.8
    A partially benzylated derivative of anhydro-D-altro-heptulose found in Coriaria japonica A, which is a synthetically useful unit, was successfully synthesized from a D-mannose derivative by a novel synthetic approach involving the intramolecular O-ketopyranosylation reaction developed by us. This synthetic approach was also applicable to the preparation of its four analogs. (C) 2008 Elsevier Ltd. All rights reserved.
  • Synthesis of a partially benzylated derivative of the anhydro-d-altro-heptulose found in Coriaria japonica A
    作者:Sho Matsuda、Kazuhide Matsumura、Mikio Watanabe、Takashi Yamanoi
    DOI:10.1016/j.tetlet.2007.06.057
    日期:2007.8
    A partially benzylated derivative of the anhydro-D-altro-heptulose found in Coriaria japonica A, which is a synthetically useful unit, was successfully synthesized from a D-mannose derivative by a novel synthetic approach involving an intramolecular O-ketopyranosylation. (c) 2007 Elsevier Ltd. All rights reserved.
查看更多