(1S,2R,3S)-1-(2-furyl)-2-^tbutyldimethylsiloxy-3-chlorobutanol | 1040921-83-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 杂芳族化合物
• 英文名称: (1S,2R,3S)-1-(2-furyl)-2-^tbutyldimethylsiloxy-3-chlorobutanol
• 英文别名: (1S,2R,3S)-2-[tert-butyl(dimethyl)silyl]oxy-3-chloro-1-(furan-2-yl)butan-1-ol
• CAS: 1040921-83-2
• 化学式: C₁₄H₂₅ClO₃Si
• 分子量: 304.889
• InChiKey: BQLPSZNZYRSMIH-UHTWSYAYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.33
• 重原子数：
  19
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  42.6
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (1S,2R,3S)-1-(2-furyl)-2-^tbutyldimethylsiloxy-3-chlorobutanol 、 乙烯基乙醚 在 4-甲基苯磺酸吡啶 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 生成
  参考文献：
  名称：

  Total synthesis of (+)-asperlin

  摘要：

  Syntheses of (+)-asperlin 1 were achieved via two different synthetic routes. 1,2-Addition of alpha-furyl anion to (2R,3S)-2-'butyldimethylsilyloxy-3-chlorobutanal 6 gave (1S,2R,3S)-1-(2-furyl)-2-'butyldimethylsilyloxy-3-chlorobutanol 7, which was converted to the chiral intermediate, (1S,2R,3R)-1-(2-furyl)-2,3-epoxybutanol 8 (37% overall yield from 6) for the synthesis of (+)-1. The second synthesis of (+)-asperlin 1 from (2R,3S)-6 was achieved in 8% overall yield, based on a combination of the indium-assisted stereoselective addition of 3-bromopropenyl acetate 9 to (2R,3S)-6 and the ring closing metathesis (RCM) using Grubbs catalyst. (C) 2008 Elsevier Ltd. All riehts reserved.

  DOI：

  10.1016/j.tetasy.2008.04.011
• 作为产物：
  描述：

  呋喃 、 (±)-trans-2-((tert-butyldimethylsilyl)oxy)-3-chlorobutanal 在 正丁基锂 作用下， 以 四氢呋喃 、 正戊烷 为溶剂， 反应 2.17h， 以72%的产率得到(1S,2R,3S)-1-(2-furyl)-2-^tbutyldimethylsiloxy-3-chlorobutanol
  参考文献：
  名称：

  Total synthesis of (+)-asperlin

  摘要：

  Syntheses of (+)-asperlin 1 were achieved via two different synthetic routes. 1,2-Addition of alpha-furyl anion to (2R,3S)-2-'butyldimethylsilyloxy-3-chlorobutanal 6 gave (1S,2R,3S)-1-(2-furyl)-2-'butyldimethylsilyloxy-3-chlorobutanol 7, which was converted to the chiral intermediate, (1S,2R,3R)-1-(2-furyl)-2,3-epoxybutanol 8 (37% overall yield from 6) for the synthesis of (+)-1. The second synthesis of (+)-asperlin 1 from (2R,3S)-6 was achieved in 8% overall yield, based on a combination of the indium-assisted stereoselective addition of 3-bromopropenyl acetate 9 to (2R,3S)-6 and the ring closing metathesis (RCM) using Grubbs catalyst. (C) 2008 Elsevier Ltd. All riehts reserved.

  DOI：

  10.1016/j.tetasy.2008.04.011

文献信息

• Total synthesis of (+)-asperlin
  作者：Hideaki Akaike、Hidekazu Horie、Keisuke Kato、Hiroyuki Akita

  DOI：10.1016/j.tetasy.2008.04.011

  日期：2008.5

  Syntheses of (+)-asperlin 1 were achieved via two different synthetic routes. 1,2-Addition of alpha-furyl anion to (2R,3S)-2-'butyldimethylsilyloxy-3-chlorobutanal 6 gave (1S,2R,3S)-1-(2-furyl)-2-'butyldimethylsilyloxy-3-chlorobutanol 7, which was converted to the chiral intermediate, (1S,2R,3R)-1-(2-furyl)-2,3-epoxybutanol 8 (37% overall yield from 6) for the synthesis of (+)-1. The second synthesis of (+)-asperlin 1 from (2R,3S)-6 was achieved in 8% overall yield, based on a combination of the indium-assisted stereoselective addition of 3-bromopropenyl acetate 9 to (2R,3S)-6 and the ring closing metathesis (RCM) using Grubbs catalyst. (C) 2008 Elsevier Ltd. All riehts reserved.