methyl 2,3,4-tri-O-acetyl-6-S-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl)-6-thio-α-D-glucopyranoside

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: methyl 2,3,4-tri-O-acetyl-6-S-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl)-6-thio-α-D-glucopyranoside
• 英文别名: [(2S,3S,4S,5R,6S)-2-[[(2R,4aR,6S,7S,8S,8aR)-2-phenyl-7,8-bis(phenylmethoxy)-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]sulfanylmethyl]-4,5-diacetyloxy-6-methoxyoxan-3-yl] acetate
• 化学式: C₄₀H₄₆O₁₃S
• 分子量: 766.863
• InChiKey: XJDTYTBXECGEHD-IVTLTPFRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  54
• 可旋转键数：
  17
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  169
• 氢给体数：
  0
• 氢受体数：
  14

反应信息

• 作为产物：
  描述：

  methyl 2,3,4-tri-O-acetyl-α-D-glucopyranose 在 2,6-二叔丁基-4-甲基吡啶 、 三氟甲磺酸酐 、 一水合肼 、 溶剂黄146 、 三苯基膦 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 6.83h， 生成 methyl 2,3,4-tri-O-acetyl-6-S-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl)-6-thio-α-D-glucopyranoside
  参考文献：
  名称：

  Direct Stereoselective Synthesis of β-Thiomannosides

  摘要：

  A highly diastereoselective synthesis of beta-thiomannopyranosides is described in which S-phenyl 2,3-di-0-benzyl-4,6-O-benzylidene-1-deoxy-1-thia-alpha-D-mannopyranoside S-oxide is treated with triflic anhydride and 2,6-di-tert-butyl-4-methylpyridine in CH2Cl2 at -78 degrees C leading to the formation of an intermediate alpha-mannosyl triflate. Addition of primary, secondary, or tertiary thiols then leads to the beta-thiomannosides, by an S(N)2-like displacement, in good yield and with excellent stereoselectivity. Deprotection is achieved either by Birch reduction or by Zemplen deacetylation, of the acetyl protected aglycons, followed by hydrogenolysis over Pearlman's catalyst. The assignment of configuration of the beta-thiomannopyranosides is discussed in terms of the chemical shift of the mannose H5 resonance and the (1)J(CH) of the mannose anomeric carbon.

  DOI：

  10.1021/jo9914667

文献信息

• Direct Stereoselective Synthesis of β-Thiomannosides
  作者：David Crich、Hongmei Li

  DOI：10.1021/jo9914667

  日期：2000.2.1

  A highly diastereoselective synthesis of beta-thiomannopyranosides is described in which S-phenyl 2,3-di-0-benzyl-4,6-O-benzylidene-1-deoxy-1-thia-alpha-D-mannopyranoside S-oxide is treated with triflic anhydride and 2,6-di-tert-butyl-4-methylpyridine in CH2Cl2 at -78 degrees C leading to the formation of an intermediate alpha-mannosyl triflate. Addition of primary, secondary, or tertiary thiols then leads to the beta-thiomannosides, by an S(N)2-like displacement, in good yield and with excellent stereoselectivity. Deprotection is achieved either by Birch reduction or by Zemplen deacetylation, of the acetyl protected aglycons, followed by hydrogenolysis over Pearlman's catalyst. The assignment of configuration of the beta-thiomannopyranosides is discussed in terms of the chemical shift of the mannose H5 resonance and the (1)J(CH) of the mannose anomeric carbon.