(2S,3S)-pent-4-ene-2,3-diol | 132039-54-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2S,3S)-pent-4-ene-2,3-diol
• CAS: 132039-54-4
• 化学式: C₅H₁₀O₂
• 分子量: 102.133
• InChiKey: NVEPXBVOEVVLHX-WHFBIAKZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0
• 重原子数：
  7
• 可旋转键数：
  2
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  40.5
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (2S,3S)-pent-4-ene-2,3-diol 在 RuCl2(1,3-dimesityl-imidazolidin-2-yl)(PCy3)(=CHPh) 、 4-二甲氨基吡啶 、 对甲苯磺酸 、 N,N'-二环己基碳二亚胺 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 6.0h， 生成 拟茎点菌内酯B
  参考文献：
  名称：

  A cross-metathesis approach to the synthesis of (+)-phomopsolide B

  摘要：

  The synthesis of phomopsolide B has been achieved using an olefin cross-metathesis (CM) reaction as key step. Two metathesis partners, enediol and 5-hydroxy vinyl lactone were prepared from L-ascorbic acid. This is the first report of using 5-hydroxy vinyl lactone in an olefin cross-metathesis reaction. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2015.05.032
• 作为产物：
  描述：

  戊-4-烯-2,3-二醇 生成 (2S,3S)-pent-4-ene-2,3-diol
  参考文献：
  名称：

  Lipase-catalyzed kinetic resolution of threo -configured 1,2-diols: a comparative study of transesterification versus hydrolysis

  摘要：

  The kinetic resolution of the alpha,beta-unsaturated vicinal diols 3 has been investigated by irreversible transesterification in organic media and by hydrolysis of the corresponding diacetates 6 (Scheme 1). The best results were obtained in the hydrolysis of the diacetates with the lipase CAL-B from Candida antarctica as a catalyst. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0957-4166(98)00043-3

文献信息

• Tandem Ring-Closing/Cross-Metathesis Approach for the Synthesis of Synargentolide B and Its Stereoisomers
  作者：Gowravaram Sabitha、Kontham Shankaraiah、Jhillu S. Yadav

  DOI：10.1002/ejoc.201300434

  日期：2013.8

  stereoisomers have been accomplished from L-(+)- and D-(–)-diethyl tartrates, D-ribose, and D-mannitol as chiral pool starting materials. The key step was a tandem ring-closing/cross-metathesis reaction in which lactone formation and fragment coupling were accomplished in one pot. The spectroscopic data of synthetic product 2c were in agreement with those reported for the natural product. Synargentolide

  以 L-(+)- 和 D-(-)-酒石酸二乙酯、D-核糖和 D-甘露醇为手性池起始材料，已完成了合成内酯 B 及其三种立体异构体的立体选择性合成。关键步骤是串联闭环/交叉复分解反应，其中内酯形成和片段偶联在一锅中完成。合成产物 2c 的光谱数据与天然产物报道的数据一致。由 Rivett 等人分离的 Synargentolide B。和 Pereda-Miranda 等人分离的化合物。不是非对映异构体，而是相同的。
• Bacterial Biotransformation of Isoprene and Related Dienes
  作者：Derek R. Boyd、David Clarke、Marcel C. Cleij、John T. G Hamilton、Gary N. Sheldrake

  DOI：10.1007/s007060070096

  日期：2000.6.15

  Pseudomonas putida ML 2 was used in the oxidative biodegradation of the acyclic dienes isoprene, trans -piperylene, cis -piperylene, and 1,3-butadiene. Regioselective dioxygenase-catalyzed dihydroxylation of alkenes yielded vicinal diols in the preferred sequence monosubstituted >  cis -disubstituted >  gem -disubstituted >  trans -disubstituted. The isolated diol metabolites had an excess of the R

   细菌 恶臭假单胞菌 在无环二烯烃的氧化降解，使用ML 2异戊二烯， 反式 -piperylene， 顺 -piperylene，和1,3-丁二烯。区域选择性双加氧酶催化的烯烃的二羟基化产生邻位二醇，优选的顺序为单取代>  顺式- 二取代>  宝石- 二取代>  反式- 二取代。分离出的二醇代谢物具有过量的 R 构型（9–97％ ee ），并通过加入丙二醇作为抑制剂来控制进一步的二醇氧化。使用ML2菌株的立体选择性是由于酶的不对称烯烃二羟基化和二醇的动力学拆分而产生的。 R 构型的烯丙基仲醇基团的对映选择性氧化产生相应的不饱和酮醇 。回收的残留二醇的 S 构型大大过量（≥93％ ee ） 。除了产生不饱和二醇和酮醇的酶二烯氧化步骤之外，还发现了酶烯加氢产生饱和酮醇和二醇的证据。
• A Universal Strategy for Synthesis of Agropyrenol Family. Total Synthesis of Agropyrenol, Sordarial, and Heterocornol A and B
  作者：Martin Markovič、Peter Koóš、Saskia Sokoliová、Nikola Boháčiková、Tomáš Vyskočil、Ján Moncoľ、Tibor Gracza

  DOI：10.1021/acs.joc.2c02092

  日期：2022.12.2

  A divergent strategy for natural polyketides synthesis has been designed. This synthetic route allowed chemical alterations leading to all stereoisomers of the natural agropyrenol 1, sordarial 2, and heterocornol B 4. Key steps involve desymmetrization of divinylcarbinol using asymmetric Sharpless epoxidation and Heck coupling of an easily available aromatic partner and prepared chiral alkene. The

  设计了天然聚酮化合物合成的发散策略。这种合成路线允许进行化学改变，从而生成天然农芘酚1、sordarial 2和异木酚 B 4的所有立体异构体。关键步骤包括使用不对称 Sharpless 环氧化对二乙烯基甲醇进行去对称化，以及将一种易于获得的芳香族伴侣与制备的手性烯烃进行 Heck 偶联。合成方法的通用性在异木酚A 3和sordariol 5的制备中得到了证明。制备的天然化合物2 ·1/3C 6 H 12和4的绝对和相对构型通过单晶X射线分析确认和分配。
• Olefin cross-metathesis based approach for the first total synthesis of phomopsolidone B and total synthesis of phomopsolidone A
  作者：Kasa Shiva Raju、Gowravaram Sabitha

  DOI：10.1016/j.tetasy.2016.06.002

  日期：2016.8

  The first total synthesis of phomopsolidone B and the total synthesis of phomopsolidone A have been achieved based on an olefin cross-metathesis approach starting from L-(+)-diethyl tartrate. (C) 2016 Elsevier Ltd. All rights reserved.
• Xu, Daqiang; Crispino, Gerard A.; Sharpless, K. Barry, Journal of the American Chemical Society, 1992, vol. 114, # 19, p. 7570 - 7571
  作者：Xu, Daqiang、Crispino, Gerard A.、Sharpless, K. Barry

  DOI：——

  日期：——