methyl (3R,4R,5S,6S)-6-chloro-3,4-O-cyclohexylidene-3,4,5-trihydroxy-1-cyclohexene-1-carboxylate | 1054623-14-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: methyl (3R,4R,5S,6S)-6-chloro-3,4-O-cyclohexylidene-3,4,5-trihydroxy-1-cyclohexene-1-carboxylate
• 英文别名: methyl (3aS,4S,5S,7aR)-5-chloro-4-hydroxy-3a,4,5,7a-tetrahydrospiro[benzo[d][1,3]dioxole-2,1'-cyclohexane]-6-carboxylate；methyl (3aR,6S,7S,7aS)-6-chloro-7-hydroxyspiro[3a,6,7,7a-tetrahydro-1,3-benzodioxole-2,1'-cyclohexane]-5-carboxylate
• CAS: 1054623-14-1
• 化学式: C₁₄H₁₉ClO₅
• 分子量: 302.755
• InChiKey: FSHVISHVPZXZBV-WRWGMCAJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.79
• 拓扑面积：
  65
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  methyl (3R,4R,5S,6S)-6-chloro-3,4-O-cyclohexylidene-3,4,5-trihydroxy-1-cyclohexene-1-carboxylate 在 三氟乙酸 作用下， 以 甲醇 为溶剂， 反应 48.0h， 以76%的产率得到methyl (3R,4R,5S,6S)-6-chloro-3,4,5-trihydroxy-1-cyclohexene-1-carboxylate
  参考文献：
  名称：

  Determination of the absolute configuration of the cytotoxic natural product pericosine D

  摘要：

  The synthesis of two diastereomers of pericosine A from (-)-quinic acid was achieved, thus enabling the confirmation of the relative configuration and elucidation of the absolute stereochemistry of cytotoxic natural product pericosine D assigned as methyl (3R,4R,5S,6R)-6-chloro-3,4,5-trihydroxy-1-cyclohexene-1-carboxylate. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2008.06.008
• 作为产物：
  描述：

  methyl shikimate 在 吡啶 、 盐酸 、 4-二甲氨基吡啶 、 oxone 、 camphor-10-sulfonic acid 、 cesium acetate 、 碳酸氢钠 作用下， 以 四氢呋喃 、 乙醚 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 5.0h， 生成 methyl (3R,4R,5S,6S)-6-chloro-3,4-O-cyclohexylidene-3,4,5-trihydroxy-1-cyclohexene-1-carboxylate
  参考文献：
  名称：

  An Electrophilic Natural Product Provides a Safe and Robust Odor Neutralization Approach To Counteract Malodorous Organosulfur Metabolites Encountered in Skunk Spray

  摘要：

  The anal secretions of skunks comprise several types of malodorous organosulfur compounds. The pungent metabolites are used defensively by skunks to repel threats posed by predators, and in many parts of the world, those perceived threats include humans and their pets. The extremely low thresholds for detection of the organosulfur metabolites make efforts to "de-skunk" people, animals, and clothing a process fraught with many challenges. The fungal-derived metabolite pericosine A (4) is a promiscuous yet stabile electrophilic compound that we propose is used by some fungi as a novel form of chemical defense. Our investigations have indicated that pericosine A readily reacts with skunk-spray secretions to transform them into odorless products. Mechanistic and computational studies suggested that pericosine A and its synthetic analogues react via S_N2'-type mechanisms with thiols and thioacetates under aqueous conditions to generate stable thioethers. Testing revealed that pericosine A did not cause skin or eye irritation and was highly effective at deodorizing skunk anal gland secretions when formulated to include adjunctive cosmetic ingredients.

  DOI：

  10.1021/acs.jnatprod.9b00415

文献信息

• Synthesis of (−)-pericosine B, the antipode of the cytotoxic marine natural product
  作者：Yoshihide Usami、Kentaro Suzuki、Koji Mizuki、Hayato Ichikawa、Masao Arimoto

  DOI：10.1039/b813072h

  日期：——

  The stereoselective synthesis of (−)-pericosine B, which is the antipode of the cytotoxic metabolite of the fungus Periconia byssoides OUPS-N133 separated from the sea hare, was accomplished in 9 steps in 12% total yield from (−)-quinic acid, together with the synthesis of its epimer. Every crucial step of this total synthesis, including ring opening of a β-epoxide and NaBH4reduction of an unstable

  与海兔分离的真菌（Periconia byssoides OUPS-N133）的细胞毒性代谢产物的对映体（-）-pericosine B的立体选择性合成以9步完成，从（-）-奎宁酸的总收率为12％ ，连同其差向异构体的合成。整个合成过程中的每个关键步骤，包括β-环氧化物的开环和不稳定的β，γ-不饱和烯酮的NaBH 4还原，都具有出色的立体选择性。
• Synthesis of Marine Natural Product (−)-Pericosine E
  作者：Koji Mizuki、Kaoru Iwahashi、Naoko Murata、Mayuko Ikeda、Yutaka Nakai、Hiroki Yoneyama、Shinya Harusawa、Yoshihide Usami

  DOI：10.1021/ol501631r

  日期：2014.7.18

  The first synthesis of (−)-pericosine E (6), a metabolite of the Periconia byssoides OUPS-N133 isolated originally from the sea hare Aplysia kurodai, has been achieved. Efficient and regioselective synthetic procedures for the synthesis of key intermediates, anti- and syn-epoxides 9 and 10, were developed using an anti-epoxidation of diene 12 with TFDO and a bromohydrination of 12 with NBS in CH3CN/H2O

  已实现（-）-pericosine E（6）的首次合成，E-pericosine E（6）是最初从海兔Aplysia kurodai分离得到的Periconia byssoides OUPS-N133的代谢物。为关键中间体的合成，有效和区域选择性的合成方法的抗与顺式环氧化物9和10，分别使用开发抗二烯-epoxidation 12与TFDO和的bromohydrination 12与NBS在CH 3 CN / H 2 O（ 2：3）。此外，合成6的特定旋光度比较天然6阐明，天然优选的Percosine E对映异构体具有与由氯代醇（-）- 8和抗环氧（+）- 9合成的（-）- 6相同的绝对构型。