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methyl 6-O-acetyl-2,3-dideoxy-2-C-bis(methoxycarbonyl)methyl-3-C-nitro-α-D-mannopyranoside | 294190-43-5

中文名称
——
中文别名
——
英文名称
methyl 6-O-acetyl-2,3-dideoxy-2-C-bis(methoxycarbonyl)methyl-3-C-nitro-α-D-mannopyranoside
英文别名
——
methyl 6-O-acetyl-2,3-dideoxy-2-C-bis(methoxycarbonyl)methyl-3-C-nitro-α-D-mannopyranoside化学式
CAS
294190-43-5
化学式
C14H21NO11
mdl
——
分子量
379.321
InChiKey
KAPGTTSWWCZRMJ-CLVJZBSMSA-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):
    -1.49
  • 重原子数:
    26.0
  • 可旋转键数:
    7.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    160.73
  • 氢给体数:
    1.0
  • 氢受体数:
    11.0

反应信息

  • 作为反应物:
    描述:
    methyl 6-O-acetyl-2,3-dideoxy-2-C-bis(methoxycarbonyl)methyl-3-C-nitro-α-D-mannopyranoside甲基磺酰氯三乙胺 作用下, 以 various solvent(s) 为溶剂, 反应 4.0h, 以22%的产率得到methyl 6-O-acetyl-2,3,4-trideoxy-2-C-bis(methoxycarbonyl)methyl-3-C-nitro-α-D-threo-hex-3-enopyranoside
    参考文献:
    名称:
    Michael reactions on conformationally flexible methyl 3-C-nitro-hex-2-enopyranoside derivatives
    摘要:
    Dimethyl malonate and dibenzoylmethane attacked the C-2 position of the title 3-nitro-2-enopyranosides from the side opposite the anomeric methoxyl group to afford the 3-enopyranosides (S(N)2' products). In the case of 2,4-pentanedione and ethyl acetoacetate, further intramolecular cyclization occurred to yield dihydropyran derivatives. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(00)00075-6
  • 作为产物:
    参考文献:
    名称:
    Michael reactions on conformationally flexible methyl 3-C-nitro-hex-2-enopyranoside derivatives
    摘要:
    Dimethyl malonate and dibenzoylmethane attacked the C-2 position of the title 3-nitro-2-enopyranosides from the side opposite the anomeric methoxyl group to afford the 3-enopyranosides (S(N)2' products). In the case of 2,4-pentanedione and ethyl acetoacetate, further intramolecular cyclization occurred to yield dihydropyran derivatives. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(00)00075-6
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