(1S)-1-[(3aR,5R,6S,6aR)-2,2-dimethyl-6-phenylmethoxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]prop-2-en-1-ol | 106221-09-4

• 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: (1S)-1-[(3aR,5R,6S,6aR)-2,2-dimethyl-6-phenylmethoxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]prop-2-en-1-ol
• CAS: 106221-09-4
• 化学式: C₁₇H₂₂O₅
• 分子量: 306.359
• InChiKey: SBMVXWWAOMFYLX-ZVDSWSACSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  22
• 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：
  57.2
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (1S)-1-[(3aR,5R,6S,6aR)-2,2-dimethyl-6-phenylmethoxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]prop-2-en-1-ol 在 臭氧 、 溶剂黄146 、 间氯过氧苯甲酸 作用下， 以 吡啶 、 甲醇 、 乙醚 、 二氯甲烷 、 水 为溶剂， 反应 20.0h， 生成 methyl (acetyl 2,4-di-O-acetyl-3-O-benzyl-α,β-L-idopyranoside)uronate
  参考文献：
  名称：

  New accesses to l-iduronyl synthons

  摘要：

  (PhS)(3)CLi adds with a total L-ido selectivity onto 3-O-benzyl-1,2-O-isopropylidene-alpha-D-xylo-dialdose 2, opening the way to the most efficient preparation of 1,2,4-tri-O-acetyl-3-O-benzyl-L-iduronyl synthon 8. Alternatively, in view of combinatorial syntheses, aldehyde 2 allows a good access to vinylic L-ido and D-gluco synthons which may be converted into uronic acid by a sequence involving a new aldehyde oxidation by m-CPBA in aqueous solution. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(99)02080-8
• 作为产物：
  描述：

  (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 在 sodium periodate 、 碳酸氢钠 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 4.0h， 生成 (1S)-1-[(3aR,5R,6S,6aR)-2,2-dimethyl-6-phenylmethoxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]prop-2-en-1-ol
  参考文献：
  名称：

  Synthesis of l-α-phosphatidyl-d-myo-inositol 3,5-bisphosphate from d-glucose

  摘要：

  Efficient synthesis Of L-alpha -phosphatidyl-D-myo-inositol 3,5-bisphosphate was achieved from 1,2,5,6-diisopropylidene-D-glucose by utilizing ring-closing metathesis and catalytic OsO4 dihydroxylation. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(01)01946-3

文献信息

• A straightforward approach towards glycoamino acids and glycopeptidesviaPd-catalysed allylic alkylation
  作者：Katja Krämer、Jan Deska、Christina Hebach、Uli Kazmaier

  DOI：10.1039/b813978d

  日期：——

  Chelated enolates are versatile nucleophiles for palladium-catalysed allylic alkylations. Even with complex allylic substrates the reaction proceed without significant isomerisation. This allows the stereoselective introduction of polyhydroxylated allylic sidechains into amino acids and peptides with retention of the olefin geometry.

  螯合的烯醇盐是用于钯催化的烯丙基烷基化反应的通用亲核试剂。即使使用复杂的烯丙基底物，反应也可以进行，而无需明显的异构化。这允许将多羟基化的烯丙基侧链立体选择性地引入氨基酸和肽中，并保留了烯烃的几何形状。
• Efficient Preparation of Three Building Blocks for the Synthesis of Heparan Sulfate Fragments: Towards the Combinatorial Synthesis of Oligosaccharides from Hypervariable Regions
  作者：Ollivier Gavard、Yaël Hersant、Jocelyne Alais、Véronique Duverger、Anna Dilhas、Alison Bascou、David Bonnaffé

  DOI：10.1002/ejoc.200300254

  日期：2003.9

  described. The L-iduronyl and D-glucuronyl disaccharides 1−3 were then prepared from these compounds, by means of efficient and regioselective protective group manipulations. These disaccharides form the basis of a combinatorial approach toward the synthesis of heparan sulfate fragments representative of the heterogeneous regions of this polysaccharide. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim

  描述了获得适当保护的 L-艾杜糖醛酸单糖供体 4 和 5 以及 2-叠氮葡萄糖受体 6 和 7 的新的多克路线。然后通过有效和区域选择性的保护基操作，从这些化合物制备 L-艾杜糖醛酸和 D-葡萄糖醛酸二糖 1-3。这些二糖构成了合成代表这种多糖异质区域的硫酸乙酰肝素片段的组合方法的基础。(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
• On the communication of chirality from furanose and pyranose rings to monosaccharide side chains: anomalous results in the glucose series
  作者：Samuel J. danishefsky、Michael P. DeNinno、Gary B. Phillips、Robert E. Zelle、Paul A. Lartey

  DOI：10.1016/s0040-4020(01)90570-8

  日期：1986.1
• Intra-molecular nitrone–olefin cycloaddition of d-glucose derived allylic alcohol: synthesis of new aminocyclohexitols
  作者：Chaitali Chakraborty、Vinod P. Vyavahare、Dilip D. Dhavale

  DOI：10.1016/j.tet.2007.09.011

  日期：2007.11

  Diastereo- and regioselelective intra-molecular nitrone-olefin cycloaddition reaction of in situ generated N-benzylnitrones, obtained from D-glucose derived precursors 5a/5b furnished dihydroxy functionalized isoxazolidines. The N-O bond reductive cleavage and removal of N/O-benzyl groups led to the formation of stereochemically well defined aminocyclohexitols. (c) 2007 Elsevier Ltd. All rights reserved.