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methyl 4,6-O-benzylidene-2-deoxy-2-morpholino-α-D-altropyranoside | 1607435-20-0

中文名称
——
中文别名
——
英文名称
methyl 4,6-O-benzylidene-2-deoxy-2-morpholino-α-D-altropyranoside
英文别名
——
methyl 4,6-O-benzylidene-2-deoxy-2-morpholino-α-D-altropyranoside化学式
CAS
1607435-20-0
化学式
C18H25NO6
mdl
——
分子量
351.4
InChiKey
CUSOSLDIDXAGNG-DXVYANPOSA-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

反应信息

  • 作为反应物:
    描述:
    methyl 4,6-O-benzylidene-2-deoxy-2-morpholino-α-D-altropyranoside偶氮二甲酸二异丙酯三苯基膦叠氮磷酸二苯酯 作用下, 以 四氢呋喃 为溶剂, 反应 24.33h, 以69%的产率得到methyl 3-azido-4,6-O-benzylidene-2,3-dideoxy-2-morpholino-α-D-mannopyranoside
    参考文献:
    名称:
    Preparation of new type of organocatalysts having a carbohydrate scaffold
    摘要:
    The synthesis of nine new, bifunctional organocatalysts having carbohydrate scaffolds has been accomplished. In these catalysts both of the catalytic amino and thiourea functions are directly attached to a carbohydrate core. The activities of the newly prepared catalysts were tested in a Michael addition. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2013.12.026
  • 作为产物:
    描述:
    吗啉甲基2,3-脱水-4,6-O-亚苄基-Alpha-D-吡喃糖苷 在 lithium perchlorate 作用下, 以 乙腈 为溶剂, 反应 24.0h, 以84%的产率得到methyl 4,6-O-benzylidene-2-deoxy-2-morpholino-α-D-altropyranoside
    参考文献:
    名称:
    Preparation of new type of organocatalysts having a carbohydrate scaffold
    摘要:
    The synthesis of nine new, bifunctional organocatalysts having carbohydrate scaffolds has been accomplished. In these catalysts both of the catalytic amino and thiourea functions are directly attached to a carbohydrate core. The activities of the newly prepared catalysts were tested in a Michael addition. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2013.12.026
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