phenyl 2,3,4,6-tetradeoxy-4-<(2,4-dinitrophenyl)dithio>-1-thio-α-D-erythro-hex-2-enopyranoside | 134262-66-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: phenyl 2,3,4,6-tetradeoxy-4-<(2,4-dinitrophenyl)dithio>-1-thio-α-D-erythro-hex-2-enopyranoside
• 英文别名: (2R,3S,6R)-3-(2,4-dinitrophenyl)sulfanyl-2-methyl-6-phenylsulfanyl-3,6-dihydro-2H-pyran
• CAS: 134262-66-1
• 化学式: C₁₈H₁₆N₂O₅S₂
• 分子量: 404.467
• InChiKey: UCXOYYUWTYJGMZ-PZPSRYQVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  27
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  152
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  phenyl 2,3,4,6-tetradeoxy-4-<(2,4-dinitrophenyl)dithio>-1-thio-α-D-erythro-hex-2-enopyranoside 在 吡啶 、 三苯基膦氢溴酸盐 、 sodium hydride 、 sodium cyanoborohydride 、 magnesium sulfate 、 potassium carbonate 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 二乙胺 、 间氯过氧苯甲酸 、 异丙醇 、 乙硫醇 、 肼 作用下， 以 四氢呋喃 、 甲醇 、 乙醇 、 二氯甲烷 、 苯 为溶剂， 反应 2.0h， 生成 methyl 4,6-dideoxy-4-<<(2,4,6-trideoxy-3-O-<(1,1-dimethylethyl)dimethylsilyl>-4-(methylthio)-β-D-ribo-hexopyranosyl)oxy><2-(trimethylsilyl)ethoxycarbonyl>amino>-2-O-<2,4-dideoxy-3-O-methyl-4-<(1-methylethyl)amino>-α-L-threo-pentopyranosyl>-3-O-...
  参考文献：
  名称：

  The synthesis of the core trisaccharide of esperamicin: corroboration of the proposed structure for its rearrangement product and stabilization of the core trisaccharide domain

  摘要：

  DOI：

  10.1021/ja00013a065
• 作为产物：
  描述：

  D-三乙酰半乳糖烯 在 lithium aluminium tetrahydride 、 四丁基溴化铵 、 sodium methylate 、 四氯化锡 、 二正丁基氧化锡 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 8.67h， 生成 phenyl 2,3,4,6-tetradeoxy-4-<(2,4-dinitrophenyl)dithio>-1-thio-α-D-erythro-hex-2-enopyranoside
  参考文献：
  名称：

  Studies Related to the Carbohydrate Sectors of Esperamicin and Calicheamicin: Definition of the Stability Limits of the Esperamicin Domain and Fashioning of a Glycosyl Donor from the Calicheamicin Domain

  摘要：

  The core trisaccharide regions of esperamicin and the aryltetrasaccharide region of calicheamicin have been synthesized. The minimum protection modalities necessary to stabilize structures against rearrangement to an isomeric azafuranose series were ascertained (see compounds 12 and 65). Deprotection of the 2-(trimethylsilyl)ethoxycarbonyl carbamate from 65 led to azafuranose 14 characterized as methyl glycoside 15. Using this insight, it was possible to fashion, for the first time, a pre-glycosyl donor (see compound 128) corresponding to the complete arylsaccharide sector of calicheamicin gamma(1)(I) at the oxidation level of the domain. Among the key assembly strategies were the conversion of alpha-thiophenylpseudoglycals to allal derivatives (see 44 --> 45); the interfacing of epoxide-mediated glycosylation with iodoglycosylation (see 30 --> 47 --> 48); the synthesis of hydroxylamine glycosides via triflate displacement (see 61 + 91 --> 101); and a new route to p-hydroxybenzonitriles (see formation of 86).

  DOI：

  10.1021/ja00126a013

文献信息

• Observations in the Chemistry and Biology of Cyclic Enediyne Antibiotics:  Total Syntheses of Calicheamicin γ₁^I and Dynemicin A
  作者：Samuel J. Danishefsky、Matthew D. Shair

  DOI：10.1021/jo951560x

  日期：1996.1.1
• HALCOMB, RANDALL L.;WITTMAN, MARK D.;OLSON, STEVEN H.;DANISHETSKY, SAMUEL+, J. AMER. CHEM. SOC., 113,(1991) N3, C. 5080-5082
  作者：HALCOMB, RANDALL L.、WITTMAN, MARK D.、OLSON, STEVEN H.、DANISHETSKY, SAMUEL+

  DOI：——

  日期：——
• The synthesis of the core trisaccharide of esperamicin: corroboration of the proposed structure for its rearrangement product and stabilization of the core trisaccharide domain
  作者：Randall L. Halcomb、Mark D. Wittman、Steven H. Olson、Samuel J. Danishefsky、Jerzy Golik、Henry Wong、Dolatrai Vyas

  DOI：10.1021/ja00013a065

  日期：1991.6
• Studies Related to the Carbohydrate Sectors of Esperamicin and Calicheamicin: Definition of the Stability Limits of the Esperamicin Domain and Fashioning of a Glycosyl Donor from the Calicheamicin Domain
  作者：Randall L. Halcomb、Serge H. Boyer、Mark D. Wittman、Steven H. Olson、Derek J. Denhart、Kevin K. C. Liu、Samuel J. Danishefsky

  DOI：10.1021/ja00126a013

  日期：1995.5

  The core trisaccharide regions of esperamicin and the aryltetrasaccharide region of calicheamicin have been synthesized. The minimum protection modalities necessary to stabilize structures against rearrangement to an isomeric azafuranose series were ascertained (see compounds 12 and 65). Deprotection of the 2-(trimethylsilyl)ethoxycarbonyl carbamate from 65 led to azafuranose 14 characterized as methyl glycoside 15. Using this insight, it was possible to fashion, for the first time, a pre-glycosyl donor (see compound 128) corresponding to the complete arylsaccharide sector of calicheamicin gamma(1)(I) at the oxidation level of the domain. Among the key assembly strategies were the conversion of alpha-thiophenylpseudoglycals to allal derivatives (see 44 --> 45); the interfacing of epoxide-mediated glycosylation with iodoglycosylation (see 30 --> 47 --> 48); the synthesis of hydroxylamine glycosides via triflate displacement (see 61 + 91 --> 101); and a new route to p-hydroxybenzonitriles (see formation of 86).