1-S-phenyl 2,3-di-O-(2-naphthylmethyl)-4,6-O-[1-cyano-2-(2-iodophenyl)]ethylidene-β-D-glucopyranoside | 887699-81-2

• 分子结构分类: 有机化合物
• 英文名称: 1-S-phenyl 2,3-di-O-(2-naphthylmethyl)-4,6-O-[1-cyano-2-(2-iodophenyl)]ethylidene-β-D-glucopyranoside
• 英文别名: (2S,4aR,6S,7R,8S,8aR)-2-[(2-iodophenyl)methyl]-7,8-bis(naphthalen-2-ylmethoxy)-6-phenylsulfanyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-2-carbonitrile
• CAS: 887699-81-2
• 化学式: C₄₃H₃₆INO₅S
• 分子量: 805.733
• InChiKey: DXNPCSZKEUVLFF-IVGJHFIPSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.5
• 重原子数：
  51
• 可旋转键数：
  10
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  95.2
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  1-S-phenyl 2,3-di-O-(2-naphthylmethyl)-4,6-O-[1-cyano-2-(2-iodophenyl)]ethylidene-β-D-glucopyranoside 、 甲基2,3,4-三-O-苄基-α-D-吡喃葡萄糖苷 在 molecular sieve 三氟甲磺酸酐 、 二苯基亚砜 、 2,4,5-tri-tert-butylpyrimidine 作用下， 以 二氯甲烷 为溶剂， 反应 2.5h， 生成 methyl 2,3,4-tri-O-benzyl-6-O-[2,3-di-O-(2-naphthylmethyl)-4,6-O-[1-cyano-2-(2-iodophenyl)]ethylidene-β-D-glucopyranosyl]-α-D-glucopyranoside 、 methyl 2,3,4-tri-O-benzyl-6-O-[2,3-di-O-(2-naphthylmethyl)-4,6-O-[1-cyano-2-(2-iodophenyl)]ethylidene-α-D-glucopyranosyl]-α-D-glucopyranoside
  参考文献：
  名称：

  4,6-O-[1-Cyano-2-(2-iodophenyl)ethylidene] Acetals. Improved Second-Generation Acetals for the Stereoselective Formation of β-d-Mannopyranosides and Regioselective Reductive Radical Fragmentation to β-d-Rhamnopyranosides. Scope and Limitations

  摘要：

  The [1-cyano-2-(2-iodophenyl)]ethylidene group is introduced as an acetal-protecting group for carbohydrate thioglycoside donors. The group is easily introduced under mild conditions, over short reaction times, and in the presence of a wide variety of other protecting groups by the reaction of the 4,6-diol with triethyl (2-iodophenyl)orthoacetate and camphorsulfonic acid, followed by trimethylsilyl cyanide and boron trifluoride etherate. The new protecting group conveys strong beta-selectivity with thiomannoside donors and undergoes a tin-mediated radical fragmentation to provide high yields of the synthetically challenging beta-rhamnopyranosides. The method is also applicable to the glucopyranosides when high beta-selectivity is observed in the coupling reaction and alpha-quinovosides are formed selectively in the radical fragmentation step. In the galactopyranoside series, beta-glycosides are formed selectively on coupling to donors protected by the new system, but the radical fragmentation is unselective and gives mixtures of the 4- and 6-deoxy products. Variable-temperature NMR studies for the glycosylation step, which helped define an optimal protocol, are described.

  DOI：

  10.1021/jo0526688
• 作为产物：
  描述：

  2-碘苯基乙腈 在 盐酸 、 camphor-10-sulfonic acid 作用下， 以 二氯甲烷 为溶剂， 反应 52.5h， 生成 1-S-phenyl 2,3-di-O-(2-naphthylmethyl)-4,6-O-[1-cyano-2-(2-iodophenyl)]ethylidene-β-D-glucopyranoside
  参考文献：
  名称：

  4,6-O-[1-Cyano-2-(2-iodophenyl)ethylidene] Acetals. Improved Second-Generation Acetals for the Stereoselective Formation of β-d-Mannopyranosides and Regioselective Reductive Radical Fragmentation to β-d-Rhamnopyranosides. Scope and Limitations

  摘要：

  The [1-cyano-2-(2-iodophenyl)]ethylidene group is introduced as an acetal-protecting group for carbohydrate thioglycoside donors. The group is easily introduced under mild conditions, over short reaction times, and in the presence of a wide variety of other protecting groups by the reaction of the 4,6-diol with triethyl (2-iodophenyl)orthoacetate and camphorsulfonic acid, followed by trimethylsilyl cyanide and boron trifluoride etherate. The new protecting group conveys strong beta-selectivity with thiomannoside donors and undergoes a tin-mediated radical fragmentation to provide high yields of the synthetically challenging beta-rhamnopyranosides. The method is also applicable to the glucopyranosides when high beta-selectivity is observed in the coupling reaction and alpha-quinovosides are formed selectively in the radical fragmentation step. In the galactopyranoside series, beta-glycosides are formed selectively on coupling to donors protected by the new system, but the radical fragmentation is unselective and gives mixtures of the 4- and 6-deoxy products. Variable-temperature NMR studies for the glycosylation step, which helped define an optimal protocol, are described.

  DOI：

  10.1021/jo0526688