2-{(2S,3R,4S,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-[dimethyl-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylethynyl)-silanyloxy]-tetrahydro-pyran-2-sulfonyl}-pyridine | 168985-24-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-{(2S,3R,4S,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-[dimethyl-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylethynyl)-silanyloxy]-tetrahydro-pyran-2-sulfonyl}-pyridine
• 英文别名: [(2S,3R,4S,5R,6R)-4,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)-2-pyridin-2-ylsulfonyloxan-3-yl]oxy-[2-[(2R,3R,4S,5R,6S)-6-methoxy-3,4,5-tris(phenylmethoxy)oxan-2-yl]ethynyl]-dimethylsilane
• CAS: 168985-24-8
• 化学式: C₆₃H₆₇NO₁₂SSi
• 分子量: 1090.38
• InChiKey: HIOUUMUJQVCGJU-UEIIXMTPSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  10.23
• 重原子数：
  78
• 可旋转键数：
  25
• 环数：
  9.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  148
• 氢给体数：
  0
• 氢受体数：
  13

反应信息

• 作为反应物：
  描述：

  2-{(2S,3R,4S,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-[dimethyl-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylethynyl)-silanyloxy]-tetrahydro-pyran-2-sulfonyl}-pyridine 生成 (2R,3S,4R,5R,6R)-2-(hydroxymethyl)-6-[2-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]ethyl]oxane-3,4,5-triol
  参考文献：
  名称：

  1,2-cis-C-glycoside synthesis by samarium diiodide-promoted radical cyclizations

  摘要：

  AbstractThe samarium diiodide reduction of glycosyl pyridyl sulfones bearing a silicon‐tethered unsaturated group at the C2–OH position leads to the stereo‐specific synthesis of 1,2‐cis‐C‐glycosides in good yield after desilylation. These reactions proceed via an anomeric radical with subsequent 5‐exo cyclization. Unlike the corresponding glycosyl phenyl sulfones, the pyridyl derivatives react instantaneously with samarium diiodide and do not require a cosolvent such as hexamethylphosphoramide (HMPA). Under these reaction conditions radical cyclization precedes the second reduction step. Examples of 5‐exo‐trig and ‐dig ring closures are given. The synthetic utility of this method was demonstrated by a short synthesis of methyl C‐isomaltoside.

  DOI：

  10.1002/chem.19970030822
• 作为产物：
  描述：

  methyl 2,3,4-tri-O-benzyl-6,7-dideoxy-α-D-gluco-hept-6-ynopyranoside 在 4-二甲氨基吡啶 、 正丁基锂 、 TEA 作用下， 以 四氢呋喃 、 正己烷 、 二氯甲烷 为溶剂， 反应 1.67h， 生成 2-{(2S,3R,4S,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-[dimethyl-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylethynyl)-silanyloxy]-tetrahydro-pyran-2-sulfonyl}-pyridine
  参考文献：
  名称：

  1,2-cis-C-glycoside synthesis by samarium diiodide-promoted radical cyclizations

  摘要：

  AbstractThe samarium diiodide reduction of glycosyl pyridyl sulfones bearing a silicon‐tethered unsaturated group at the C2–OH position leads to the stereo‐specific synthesis of 1,2‐cis‐C‐glycosides in good yield after desilylation. These reactions proceed via an anomeric radical with subsequent 5‐exo cyclization. Unlike the corresponding glycosyl phenyl sulfones, the pyridyl derivatives react instantaneously with samarium diiodide and do not require a cosolvent such as hexamethylphosphoramide (HMPA). Under these reaction conditions radical cyclization precedes the second reduction step. Examples of 5‐exo‐trig and ‐dig ring closures are given. The synthetic utility of this method was demonstrated by a short synthesis of methyl C‐isomaltoside.

  DOI：

  10.1002/chem.19970030822

文献信息

• Mazeas, Daniel; Skrydstrup, Troels; Doumeix, Olivier, Angewandte Chemie, 1994, vol. 106, # 13, p. 1457 - 1459
  作者：Mazeas, Daniel、Skrydstrup, Troels、Doumeix, Olivier、Beau, Jean-Marie

  DOI：——

  日期：——