(E)-S-phenyl 3-(((4'R,5'S)-5'-(R)-2'',2''-dimethyl-1'',3''-dioxolan-4''-yl)-2',2'-dimethyl-1',3'-dioxolan-4'-yl)prop-2-enethioate | 911826-80-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯硫酚酯
• 英文名称: (E)-S-phenyl 3-(((4'R,5'S)-5'-(R)-2'',2''-dimethyl-1'',3''-dioxolan-4''-yl)-2',2'-dimethyl-1',3'-dioxolan-4'-yl)prop-2-enethioate
• 英文别名: S-phenyl (E)-3-[(4R,5S)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-1,3-dioxolan-4-yl]prop-2-enethioate
• CAS: 911826-80-7
• 化学式: C₁₉H₂₄O₅S
• 分子量: 364.463
• InChiKey: XHQMARKQAUNLNJ-RPUDDXGHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  25
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  79.3
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  (E)-S-phenyl 3-(((4'R,5'S)-5'-(R)-2'',2''-dimethyl-1'',3''-dioxolan-4''-yl)-2',2'-dimethyl-1',3'-dioxolan-4'-yl)prop-2-enethioate 在 硫化氢 、 三乙胺 、 potassium hexacyanoferrate(III) 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 18.0h， 生成 5-((4'S,5'R)-5'-((R)-2'',2''-dimethyl-1'',3''-dioxolan-4''-yl)-2',2'-dimethyl-1',3'-dioxolan-4'-yl)-1,2-dithiolan-3-one
  参考文献：
  名称：

  Synthesis and Cytotoxicity of Leinamycin Antibiotic Analogues

  摘要：

  A simple synthesis of 1,2-dithiolan-3-ones from alpha,beta-unsaturated thiophenyl esters is reported. Introduction of the biologically active 1,2-dithiolan-3-one-1-oxide moiety of leinamycin into aldehydo-D-arabinose 11, the uridine derivative 16, and the deoxythymidine 21 was established. An extended bioactive part of leinamycin carrying a carbon-carbon triple bond was also synthesized. All of these analogues of leinamycin showed cytotoxic activity against HeLa3 tumor cells. Interestingly, the lipophilic, silyl group-containing derivatives proved to be more active than the hydrophilic counterparts.

  DOI：

  10.1021/jm060471h
• 作为产物：
  描述：

  phenylthio-carbonyl-methylenetriphenylphosphorane 、 2,3-二氟-6-硝基苯胺 以 甲苯 为溶剂， 反应 48.0h， 以81%的产率得到(E)-S-phenyl 3-(((4'R,5'S)-5'-(R)-2'',2''-dimethyl-1'',3''-dioxolan-4''-yl)-2',2'-dimethyl-1',3'-dioxolan-4'-yl)prop-2-enethioate
  参考文献：
  名称：

  Synthesis and Cytotoxicity of Leinamycin Antibiotic Analogues

  摘要：

  A simple synthesis of 1,2-dithiolan-3-ones from alpha,beta-unsaturated thiophenyl esters is reported. Introduction of the biologically active 1,2-dithiolan-3-one-1-oxide moiety of leinamycin into aldehydo-D-arabinose 11, the uridine derivative 16, and the deoxythymidine 21 was established. An extended bioactive part of leinamycin carrying a carbon-carbon triple bond was also synthesized. All of these analogues of leinamycin showed cytotoxic activity against HeLa3 tumor cells. Interestingly, the lipophilic, silyl group-containing derivatives proved to be more active than the hydrophilic counterparts.

  DOI：

  10.1021/jm060471h

文献信息

• Incorporation of the bioactive moiety of leinamycin into thymidine
  作者：Ákos Szilágyi、István F. Pelyvás、Orsolya Majercsik、Pál Herczegh

  DOI：10.1016/j.tetlet.2004.04.011

  日期：2004.5

  A simple synthesis of 1,2-dithiolan-3-ones from alpha,beta-unsaturated thiophenyl esters has been elaborated. With the aim of introducing the biologically active 1,2-dithiolan-3-one-1-oxide moiety of leinamycin into a nucleoside, the method was successfully applied to thymidine-5'-aldehyde. (C) 2004 Elsevier Ltd. All rights reserved.
• Synthesis and Cytotoxicity of Leinamycin Antibiotic Analogues
  作者：Ákos Szilágyi、Ferenc Fenyvesi、Orsolya Majercsik、István F. Pelyvás、Ildikó Bácskay、Pálma Fehér、Judit Váradi、Miklós Vecsernyés、Pál Herczegh

  DOI：10.1021/jm060471h

  日期：2006.9.1

  A simple synthesis of 1,2-dithiolan-3-ones from alpha,beta-unsaturated thiophenyl esters is reported. Introduction of the biologically active 1,2-dithiolan-3-one-1-oxide moiety of leinamycin into aldehydo-D-arabinose 11, the uridine derivative 16, and the deoxythymidine 21 was established. An extended bioactive part of leinamycin carrying a carbon-carbon triple bond was also synthesized. All of these analogues of leinamycin showed cytotoxic activity against HeLa3 tumor cells. Interestingly, the lipophilic, silyl group-containing derivatives proved to be more active than the hydrophilic counterparts.