2-[(3S,4S,6R)-4,6-dimethoxyoxan-3-yl]isoindole-1,3-dione | 134262-61-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异吲哚及其衍生物
• 英文名称: 2-[(3S,4S,6R)-4,6-dimethoxyoxan-3-yl]isoindole-1,3-dione
• CAS: 134262-61-6
• 化学式: C₁₅H₁₇NO₅
• 分子量: 291.304
• InChiKey: NPYDDTLZPRVPBM-RWMBFGLXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.06
• 重原子数：
  21.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  65.07
• 氢给体数：
  0.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  2-[(3S,4S,6R)-4,6-dimethoxyoxan-3-yl]isoindole-1,3-dione 在 iodonium(di-γ-collidine) perchlorate 、 4 A molecular sieve 、 三氟化硼乙醚 、 间氯过氧苯甲酸 作用下， 以 二氯甲烷 、 苯 为溶剂， 反应 10.83h， 生成 methyl O-(2,4-dideoxy-2-iodo-3-O-methyl-4-phthalimido-α-L-lyxo-pyranosyl)-(1<*>2)-6-deoxy-3-O-<(4-methoxyphenyl)methyl>-β-D-galactopyranoside
  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
• 作为产物：
  描述：

  methyl 2-deoxy-β-D-erythro-pentopyranoside 在 三苯基膦 、 silver(l) oxide 、 偶氮二甲酸二乙酯 作用下， 以 丙酮 为溶剂， 生成 2-[(3S,4S,6R)-4,6-dimethoxyoxan-3-yl]isoindole-1,3-dione
  参考文献：
  名称：

  七叶红素的立体化学研究：异丙基氨基糖部分的绝对构型的确定

  摘要：

  通过比较衍生的甲醇分解产物的CD光谱与两种合成的对映糖苷和的CD光谱，确定了埃斯帕米霉素A 1异丙基氨基糖部分的绝对立体化学为-戊吡喃糖基。

  DOI：

  10.1016/s0040-4039(01)80434-2

文献信息

• 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
• 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：——