methyl (p-tolyl 5-acetamido-4,7,8,9-tetra-O-tert-butyldimethylsilyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulopyranosid)onate | 819814-50-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: methyl (p-tolyl 5-acetamido-4,7,8,9-tetra-O-tert-butyldimethylsilyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulopyranosid)onate
• CAS: 819814-50-1
• 化学式: C₄₃H₈₃NO₈SSi₄
• 分子量: 886.542
• InChiKey: CTMLMSLUMFKTSZ-PHBBSRQLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  11.44
• 重原子数：
  57.0
• 可旋转键数：
  15.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.81
• 拓扑面积：
  101.55
• 氢给体数：
  1.0
• 氢受体数：
  9.0

反应信息

• 作为反应物：
  描述：

  methyl (p-tolyl 5-acetamido-4,7,8,9-tetra-O-tert-butyldimethylsilyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulopyranosid)onate 在 四溴化碳 、 三乙胺三氧化硫 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 3.5h， 生成 methyl (p-tolyl 5-acetamido-7,8-di-O-tert-butyldimethylsilyl-3,5-dideoxy-9-O-sulfo-2-thio-D-glycero-α-D-galacto-non-2-ulopyranosid)onate sodium salt
  参考文献：
  名称：

  Chemoselective deprotection of acid labile primary hydroxyl protecting groups under CBr4-photoirradiation conditions

  摘要：

  The CBr4-photoirradiation in methanol generates a controlled source of HBr, which can chemoselectively deprotect commonly used hydroxyl-protecting groups in saccharides and nucleosides, such as tert-butyldimethylsilyl, isopropylidene, benzylidene and triphenyl ethers in the presence of other acid-labile functional groups. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2004.09.095
• 作为产物：
  描述：

  叔丁基二甲基氯硅烷 、 (2S,4S,5R,6R)-5-Acetylamino-4-hydroxy-2-p-tolylsulfanyl-6-((1R,2R)-1,2,3-trihydroxy-propyl)-tetrahydro-pyran-2-carboxylic acid methyl ester 在 lutidine 作用下， 以 二氯甲烷 为溶剂， 生成 methyl (p-tolyl 5-acetamido-4,7,8,9-tetra-O-tert-butyldimethylsilyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulopyranosid)onate
  参考文献：
  名称：

  Chemoselective deprotection of acid labile primary hydroxyl protecting groups under CBr4-photoirradiation conditions

  摘要：

  The CBr4-photoirradiation in methanol generates a controlled source of HBr, which can chemoselectively deprotect commonly used hydroxyl-protecting groups in saccharides and nucleosides, such as tert-butyldimethylsilyl, isopropylidene, benzylidene and triphenyl ethers in the presence of other acid-labile functional groups. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2004.09.095