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(2R,4S,5R,6R)-6-[(R)-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-4,5-dihydroxy-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester | 192447-82-8

中文名称
——
中文别名
——
英文名称
(2R,4S,5R,6R)-6-[(R)-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-4,5-dihydroxy-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester
英文别名
methyl (2R,4S,5R,6R)-6-[(R)-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-hydroxymethyl]-4,5-dihydroxy-2-methoxyoxane-2-carboxylate
(2R,4S,5R,6R)-6-[(R)-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-4,5-dihydroxy-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester化学式
CAS
192447-82-8
化学式
C14H24O9
mdl
——
分子量
336.339
InChiKey
KKZSFAVBUFJKHU-DLWUKCBXSA-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):
    -1.47
  • 重原子数:
    23.0
  • 可旋转键数:
    4.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    123.91
  • 氢给体数:
    3.0
  • 氢受体数:
    9.0

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

反应信息

  • 作为反应物:
    描述:
    (2R,4S,5R,6R)-6-[(R)-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-4,5-dihydroxy-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester4-二甲氨基吡啶四氧化钌 作用下, 以 吡啶四氯化碳 为溶剂, 反应 64.0h, 生成 (2R,4S)-4-Benzoyloxy-6-((R)-2,2-dimethyl-[1,3]dioxolane-4-carbonyl)-2-methoxy-3,4-dihydro-2H-pyran-2-carboxylic acid methyl ester
    参考文献:
    名称:
    Oxidation Products of C-4 and C-7 Hydroxyls in the Methyl α-Glycoside Derivatives of KDN1
    摘要:
    A regioselective protection of hydroxyl groups in the methyl ester-methyl alpha-glycoside derivative of KDN was demonstrated. Isopropylidenation of methyl (methyl 3-deoxy-alpha-D-glycero-D-galacto-2-nonulopyranosid)onate (1) gave mono- (8,9) and di- (5,7:8,9) O-isopropylidene derivatives. Benzoylation of methyl (methyl 3-deoxy-8, 9-O-isopropylidene-alpha-D-glycero-D-galacto-2 -nonulopyranosid)onate (7) gave di- (4,5) and tri- (4,5,7) O-benzoates. Through these reactions, it was found that the reactivity of the hydroxyl groups was different from that of methyl beta-glycoside of KDN. Oxidation products of C-4 and C-7 hydroxyl groups (6 and 11) were synthesized from these compounds.
    DOI:
    10.1080/07328309708007332
  • 作为产物:
    描述:
    methyl (methyl 3-deoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate2,2-二甲氧基丙烷对甲苯磺酸 作用下, 以 丙酮 为溶剂, 反应 16.0h, 以91%的产率得到(2R,4S,5R,6R)-6-[(R)-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-4,5-dihydroxy-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester
    参考文献:
    名称:
    Oxidation Products of C-4 and C-7 Hydroxyls in the Methyl α-Glycoside Derivatives of KDN1
    摘要:
    A regioselective protection of hydroxyl groups in the methyl ester-methyl alpha-glycoside derivative of KDN was demonstrated. Isopropylidenation of methyl (methyl 3-deoxy-alpha-D-glycero-D-galacto-2-nonulopyranosid)onate (1) gave mono- (8,9) and di- (5,7:8,9) O-isopropylidene derivatives. Benzoylation of methyl (methyl 3-deoxy-8, 9-O-isopropylidene-alpha-D-glycero-D-galacto-2 -nonulopyranosid)onate (7) gave di- (4,5) and tri- (4,5,7) O-benzoates. Through these reactions, it was found that the reactivity of the hydroxyl groups was different from that of methyl beta-glycoside of KDN. Oxidation products of C-4 and C-7 hydroxyl groups (6 and 11) were synthesized from these compounds.
    DOI:
    10.1080/07328309708007332
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