ethyl 6-O-tert-butyldiphenylsilyl-2-thio-β-D-fructofuranoside | 302905-13-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: ethyl 6-O-tert-butyldiphenylsilyl-2-thio-β-D-fructofuranoside
• 英文别名: TBDPS(-6)Fruf(b)-SEt；(2S,3S,4S,5R)-5-[[tert-butyl(diphenyl)silyl]oxymethyl]-2-ethylsulfanyl-2-(hydroxymethyl)oxolane-3,4-diol
• CAS: 302905-13-1
• 化学式: C₂₄H₃₄O₅SSi
• 分子量: 462.682
• InChiKey: QUAMBEVSDOSZLX-SVPADUAOSA-N

物化性质

• 沸点：
  573.2±50.0 °C(Predicted)
• 密度：
  1.20±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.13
• 重原子数：
  31
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  104
• 氢给体数：
  3
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  ethyl 6-O-tert-butyldiphenylsilyl-2-thio-β-D-fructofuranoside 在 palladium on activated charcoal 吡啶 、 咪唑 、 三乙基硅烷 、 4-二甲氨基吡啶 、 sodium hydroxide 、 Amberlite IR-45(OH-) 、 di-tert-butylmethylpyridine 、 氢气 、 四丁基硫酸氢铵 、 DMTST 、 tris(dimethylamino)sulfonium trimethylsilyldifluoride 、 三氟乙酸 作用下， 以 甲醇 、 二氯甲烷 、 氯仿 、 乙酸乙酯 、 N,N-二甲基甲酰胺 为溶剂， -35.0~20.0 ℃ 、758.44 kPa 条件下， 反应 132.0h， 生成 蔗糖
  参考文献：
  名称：

  A Novel β-Directing Fructofuranosyl Donor Concept. Stereospecific Synthesis of Sucrose

  摘要：

  A new concept for the construction of beta-D-fructofuranosides based on the idea of locking the anomeric CH2OH group to the alpha-side through an internal bridge to the 4-hydroxyl group is presented. Thioglycoside fructose donors containing an internal 1,4-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl) (TIPS) acetal bridge have been constructed and used in glycosylations with dimethyl(thiomethyl)sulfonium triflate (DMTST) as promoter. The couplings were stereospecific to give beta-D-fructofuranosyl disaccharides in high yields. Using this approach, sucrose has been synthesized stereospecifically in 80% yield.

  DOI：

  10.1021/ja001439u
• 作为产物：
  描述：

  叔丁基二苯基氯硅烷 、 ethyl 2-thio-β-D-fructofuranoside 在 吡啶 作用下， 以74%的产率得到ethyl 6-O-tert-butyldiphenylsilyl-2-thio-β-D-fructofuranoside
  参考文献：
  名称：

  A Novel β-Directing Fructofuranosyl Donor Concept. Stereospecific Synthesis of Sucrose

  摘要：

  A new concept for the construction of beta-D-fructofuranosides based on the idea of locking the anomeric CH2OH group to the alpha-side through an internal bridge to the 4-hydroxyl group is presented. Thioglycoside fructose donors containing an internal 1,4-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl) (TIPS) acetal bridge have been constructed and used in glycosylations with dimethyl(thiomethyl)sulfonium triflate (DMTST) as promoter. The couplings were stereospecific to give beta-D-fructofuranosyl disaccharides in high yields. Using this approach, sucrose has been synthesized stereospecifically in 80% yield.

  DOI：

  10.1021/ja001439u

文献信息

• A Novel β-Directing Fructofuranosyl Donor Concept. Stereospecific Synthesis of Sucrose
  作者：Stefan Oscarson、Fernando W. Sehgelmeble

  DOI：10.1021/ja001439u

  日期：2000.9.1

  A new concept for the construction of beta-D-fructofuranosides based on the idea of locking the anomeric CH2OH group to the alpha-side through an internal bridge to the 4-hydroxyl group is presented. Thioglycoside fructose donors containing an internal 1,4-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl) (TIPS) acetal bridge have been constructed and used in glycosylations with dimethyl(thiomethyl)sulfonium triflate (DMTST) as promoter. The couplings were stereospecific to give beta-D-fructofuranosyl disaccharides in high yields. Using this approach, sucrose has been synthesized stereospecifically in 80% yield.