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手性硫脲——在不对称合成和药物化学中的制备及意义。

Chiral Thioureas-Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry.

机构信息

Faculty of Chemistry, Wrocław University of Science and Technology, Wybrzeże Wyspiańskiego 27, 50 370 Wrocław, Poland.

Faculty of Chemistry, University of Wrocław, 14 F. Joliot-Curie St., 50 383 Wrocław, Poland.

出版信息

Molecules. 2020 Jan 18;25(2):401. doi: 10.3390/molecules25020401.

DOI:10.3390/molecules25020401
PMID:31963671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7024223/
Abstract

For almost 20 years, thioureas have been experiencing a renaissance of interest with the emerged development of asymmetric organocatalysts. Due to their relatively high acidity and strong hydrogen bond donor capability, they differ significantly from ureas and offer, appropriately modified, great potential as organocatalysts, chelators, drug candidates, etc. The review focuses on the family of chiral thioureas, presenting an overview of the current state of knowledge on their synthesis and selected applications in stereoselective synthesis and drug development.

摘要

近 20 年来,随着不对称有机催化剂的发展,硫脲重新引起了人们的兴趣。由于其相对较高的酸度和较强的氢键供体能力,它们与脲类有很大的不同,并具有作为有机催化剂、螯合剂、药物候选物等的巨大潜力,经过适当修饰。本文综述了手性硫脲的研究进展,概述了其合成方法及在立体选择性合成和药物开发中的应用。

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Molecules. 2015 Aug 26;20(9):15500-24. doi: 10.3390/molecules200915500.
5
Development of chiral thiourea catalysts and its application to asymmetric catalytic reactions.手性硫脲催化剂的开发及其在不对称催化反应中的应用。
Chem Pharm Bull (Tokyo). 2010 May;58(5):593-601. doi: 10.1248/cpb.58.593.
6
Aminocatalysts are More Environmentally Friendly than Hydrogen-Bonding Catalysts.手性胺催化剂比氢键催化剂更环保。
ChemSusChem. 2022 Aug 19;15(16):e202201045. doi: 10.1002/cssc.202201045. Epub 2022 Jul 5.
7
Highly enantioselective carbene insertion into N-H bonds of aliphatic amines.高对映选择性卡宾插入脂肪族伯胺中的 N-H 键。
Science. 2019 Nov 22;366(6468):990-994. doi: 10.1126/science.aaw9939.
8
Synthesis of both enantiomers of hemiesters by enantioselective methanolysis of meso cyclic anhydrides catalyzed by alpha-amino acid-derived chiral thioureas.由α-氨基酸衍生的手性硫脲催化的中环酸酐的对映选择性甲醇解合成非对映异构体的半酯。
J Org Chem. 2010 Aug 6;75(15):5417-20. doi: 10.1021/jo100792r.
9
Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles.布朗斯特酸催化的不对称多组分反应,用于方便地合成高对映选择性的结构多样的含氮杂环。
Acc Chem Res. 2011 Nov 15;44(11):1156-71. doi: 10.1021/ar2000343. Epub 2011 Jul 29.
10
Bifunctional hydrogen-bond donors that bear a quinazoline or benzothiadiazine skeleton for asymmetric organocatalysis.具有喹唑啉或苯并噻二嗪骨架的双功能氢键供体,用于不对称有机催化。
Chemistry. 2011 Sep 5;17(37):10470-7. doi: 10.1002/chem.201101338. Epub 2011 Aug 2.

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Novel Thiourea Ligands-Synthesis, Characterization and Preliminary Study on Their Coordination Abilities.新型硫脲配体——合成、表征及其配位能力的初步研究
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Design, synthesis, inhibitory activity, and molecular simulations study for d-glucose-conjugated thioureas containing pyrimidine ring as multitarget inhibitors against α-amylase, α-glucosidase, DDP-4, and PTP1B in Type 2 diabetes mellitus.含嘧啶环的d-葡萄糖共轭硫脲作为2型糖尿病中α-淀粉酶、α-葡萄糖苷酶、二肽基肽酶-4和蛋白酪氨酸磷酸酶1B多靶点抑制剂的设计、合成、抑制活性及分子模拟研究
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Isoselective Ring-Opening Polymerization of -Lactide from Chiral Takemoto's Organocatalysts: Elucidation of Stereocontrol.基于手性武本有机催化剂的丙交酯等规开环聚合:立体控制的阐释
ACS Macro Lett. 2018 Dec 18;7(12):1413-1419. doi: 10.1021/acsmacrolett.8b00852. Epub 2018 Nov 19.
2
A sustainable strategy for the synthesis of bis-2-iminothiazolidin-4-ones utilizing novel series of asymmetrically substituted bis-thioureas as viable precursors.一种利用新型不对称取代双硫脲系列作为可行前体来合成双-2-亚氨基噻唑烷-4-酮的可持续策略。
RSC Adv. 2018 Mar 15;8(19):10516-10521. doi: 10.1039/c8ra01253a. eCollection 2018 Mar 13.
3
Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress.
脱氢枞烷型双功能有机催化剂在不对称合成中的研究进展
RSC Adv. 2023 Oct 24;13(44):31047-31058. doi: 10.1039/d3ra06715g. eCollection 2023 Oct 18.
4
Unravelling Structural Dynamics, Supramolecular Behavior, and Chiroptical Properties of Enantiomerically Pure Macrocyclic Tertiary Ureas and Thioureas.解析手性纯大环叔胺和硫脲的结构动力学、超分子行为和手性光学性质。
J Org Chem. 2023 Jan 6;88(1):285-299. doi: 10.1021/acs.joc.2c02319. Epub 2022 Dec 8.
5
Syntheses and structural characterization of divalent metal complexes (Co, Ni, Pd and Zn) of sterically hindered thiourea ligand and a theoretical insight of their interaction with SARS-CoV-2 enzyme.空间位阻硫脲配体的二价金属配合物(钴、镍、钯和锌)的合成与结构表征及其与SARS-CoV-2酶相互作用的理论见解
J Mol Struct. 2023 Feb 15;1274:134442. doi: 10.1016/j.molstruc.2022.134442. Epub 2022 Oct 31.
6
Bis-Thiourea Chiral Sensor for the NMR Enantiodiscrimination of -Acetyl and -Trifluoroacetyl Amino Acid Derivatives.双硫脲手性传感器用于 NMR 对映体选择性检测 -乙酰基和 -三氟乙酰基氨基酸衍生物。
J Org Chem. 2022 Sep 16;87(18):11968-11978. doi: 10.1021/acs.joc.2c00814. Epub 2022 Sep 5.
7
Mononuclear Tricoordinate Copper(I) and Silver(I) Halide Complexes of a Sterically Bulky Thiourea Ligand and a Computational Insight of Their Interaction with Human Insulin.单核三配位卤化铜(I)和卤化银(I)配合物与一种空间位阻硫脲配体的相互作用及其与人胰岛素的计算研究。
Molecules. 2022 Jun 30;27(13):4231. doi: 10.3390/molecules27134231.
8
Asymmetric Michael Addition in Synthesis of β-Substituted GABA Derivatives.不对称迈克尔加成在β-取代 GABA 衍生物合成中的应用。
Molecules. 2022 Jun 13;27(12):3797. doi: 10.3390/molecules27123797.
9
A more sustainable isothiocyanate synthesis by amine catalyzed sulfurization of isocyanides with elemental sulfur.通过胺催化异腈与元素硫的硫化反应实现更可持续的异硫氰酸酯合成。
RSC Adv. 2021 Jan 14;11(5):3134-3142. doi: 10.1039/d0ra10436a. eCollection 2021 Jan 11.
10
Recent advances in urea- and thiourea-containing compounds: focus on innovative approaches in medicinal chemistry and organic synthesis.含尿素和硫脲化合物的最新进展:聚焦于药物化学和有机合成中的创新方法。
RSC Med Chem. 2021 May 13;12(7):1046-1064. doi: 10.1039/d1md00058f. eCollection 2021 Jul 21.
Organocatalytic Enantioselective Mannich Reaction: Direct Access to Chiral β-Amino Esters.
有机催化对映选择性曼尼希反应:直接合成手性β-氨基酯。
ACS Omega. 2019 Jan 29;4(1):2168-2177. doi: 10.1021/acsomega.8b02132. eCollection 2019 Jan 31.
4
Organocatalytic [4 + 2] cyclizations of para-quinone methide derivatives with isocyanates.有机催化的对醌甲川衍生物与异氰酸酯的[4 + 2]环化反应。
Org Biomol Chem. 2019 Jul 21;17(27):6662-6670. doi: 10.1039/c9ob00918c. Epub 2019 Jun 26.
5
Bianthryl-based organocatalysts for the asymmetric Henry reaction of fluoroketones.基于双蒽基的有机催化剂在氟代酮不对称 Henry 反应中的应用。
Org Biomol Chem. 2019 Jun 7;17(21):5244-5248. doi: 10.1039/c9ob00884e. Epub 2019 May 14.
6
Highly efficient Ir-catalyzed asymmetric hydrogenation of benzoxazinones and derivatives with a Brønsted acid cocatalyst.布朗斯特酸助催化剂用于铱催化苯并恶嗪酮及其衍生物的高效不对称氢化反应
Chem Sci. 2019 Mar 19;10(15):4328-4333. doi: 10.1039/c8sc05797d. eCollection 2019 Apr 21.
7
Catalytic Asymmetric (4+3) Cyclizations of In Situ Generated ortho-Quinone Methides with 2-Indolylmethanols.原位生成的邻醌甲醚与 2-吲哚甲醇的催化不对称 (4+3) 环化反应。
Angew Chem Int Ed Engl. 2019 Jun 24;58(26):8703-8708. doi: 10.1002/anie.201901955. Epub 2019 May 17.
8
Thiourea Modified Doxorubicin: A Perspective pH-Sensitive Prodrug.硫代尿素修饰的多柔比星:一种具有 pH 敏感性的前药。
Bioconjug Chem. 2019 Mar 20;30(3):741-750. doi: 10.1021/acs.bioconjchem.8b00885. Epub 2019 Feb 13.
9
Design, synthesis and algicides activities of thiourea derivatives as the novel scaffold aldolase inhibitors.作为新型骨架醛缩酶抑制剂的硫脲衍生物的设计、合成及杀藻活性。
Bioorg Med Chem. 2019 Mar 1;27(5):805-812. doi: 10.1016/j.bmc.2019.01.023. Epub 2019 Jan 24.
10
Sulfite-Promoted Synthesis of N-Difluoromethylthioureas via the Reaction of Azoles with Bromodifluoroacetate and Elemental Sulfur.通过唑类与溴二氟乙酸酯和单质硫反应,亚硫酸盐促进合成N-二氟甲基硫脲
Org Lett. 2019 Jan 18;21(2):545-548. doi: 10.1021/acs.orglett.8b03876. Epub 2018 Dec 31.