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benzyl 2-N-acetyl-3,6-di-O-benzyl-2-deoxy-5-O-methyl-α-D-mannofuranoside | 119870-40-5

中文名称
——
中文别名
——
英文名称
benzyl 2-N-acetyl-3,6-di-O-benzyl-2-deoxy-5-O-methyl-α-D-mannofuranoside
英文别名
N-[(2S,3S,4R,5S)-5-[(1R)-1-methoxy-2-phenylmethoxyethyl]-2,4-bis(phenylmethoxy)oxolan-3-yl]acetamide
benzyl 2-N-acetyl-3,6-di-O-benzyl-2-deoxy-5-O-methyl-α-D-mannofuranoside化学式
CAS
119870-40-5
化学式
C30H35NO6
mdl
——
分子量
505.611
InChiKey
BFEFYEJEFFPHHP-JPGUHONBSA-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):
    4.25
  • 重原子数:
    37.0
  • 可旋转键数:
    13.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    75.25
  • 氢给体数:
    1.0
  • 氢受体数:
    6.0

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
  • 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:
    benzyl 2-N-acetyl-3,6-di-O-benzyl-2-deoxy-5-O-methyl-α-D-mannofuranoside 在 palladium 10% on activated carbon 、 氢气 作用下, 以 乙醇 为溶剂, 反应 4.0h, 以90%的产率得到2-N-acetyl-2-deoxy-5-O-methyl-D-mannofuranoside
    参考文献:
    名称:
    Chemoenzymatic synthesis of C8-modified sialic acids and related α2–3- and α2–6-linked sialosides
    摘要:
    Naturally occurring 8-O-methylated sialic acids, including 8-O-methyl-N-acetylneuraminic acid and 8-O-methyl-N-glycolylneuraminic acid, along with 8-O-methyl-2-keto-3-deoxy-D-glycero-D-galactononulosonic acid (Kdn8Me) and 8-deoxy-Kdn were synthesized from corresponding 5-O-modified six-carbon monosaccharides and pyruvate using a sialic acid aldolase cloned from Pasteurella multocida strain P-1059 ( PmNanA). In addition, alpha 2-3- and alpha 2-6-linked sialyltrisaccharides containing Neu5Ac8Me and Kdn8Deoxy were also synthesized using a one-pot multienzyme approach. The strategy reported here provides an efficient approach to produce glycans containing various C8-modified sialic acids for biological evaluations. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.04.083
  • 作为产物:
    描述:
    溴甲苯吡啶 、 sodium azide 、 sodium methylate 、 sodium hydride 、 二正丁基氧化锡溶剂黄146三乙胺 作用下, 以 甲醇二氯甲烷N,N-二甲基甲酰胺甲苯 、 mineral oil 为溶剂, 反应 30.83h, 生成 benzyl 2-N-acetyl-3,6-di-O-benzyl-2-deoxy-5-O-methyl-α-D-mannofuranoside
    参考文献:
    名称:
    Chemoenzymatic synthesis of C8-modified sialic acids and related α2–3- and α2–6-linked sialosides
    摘要:
    Naturally occurring 8-O-methylated sialic acids, including 8-O-methyl-N-acetylneuraminic acid and 8-O-methyl-N-glycolylneuraminic acid, along with 8-O-methyl-2-keto-3-deoxy-D-glycero-D-galactononulosonic acid (Kdn8Me) and 8-deoxy-Kdn were synthesized from corresponding 5-O-modified six-carbon monosaccharides and pyruvate using a sialic acid aldolase cloned from Pasteurella multocida strain P-1059 ( PmNanA). In addition, alpha 2-3- and alpha 2-6-linked sialyltrisaccharides containing Neu5Ac8Me and Kdn8Deoxy were also synthesized using a one-pot multienzyme approach. The strategy reported here provides an efficient approach to produce glycans containing various C8-modified sialic acids for biological evaluations. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.04.083
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文献信息

  • AUGE, CLAUDINE;DAVID, SERGE;GAUTHERON, CHRISTINE;MALLERON, ANNIE;CAVAYE, +, NEW J. CHEM., 12,(1988) N 8-9, C. 733-744
    作者:AUGE, CLAUDINE、DAVID, SERGE、GAUTHERON, CHRISTINE、MALLERON, ANNIE、CAVAYE, +
    DOI:——
    日期:——
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