• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通过铑(II)双(三氟甲磺酰基)亚胺催化的环状重氮化合物反应,高效一锅合成新型多样的呋喃并[2,3-d]嘧啶二酮和噻吩并[2,3-d]嘧啶酮。

Efficient one-pot synthesis of novel and diverse furo[2,3-d] pyrimidinediones and thioxofuro[2,3-d] pyrimidineones by the rhodium (II) pivalate-catalyzed reactions of cyclic diazo compounds.

机构信息

School of Chemical Engineering, Yeungnam University, Gyeongsan, 712-749, Republic of Korea.

出版信息

Mol Divers. 2013 Nov;17(4):679-91. doi: 10.1007/s11030-013-9463-9. Epub 2013 Aug 2.

DOI:10.1007/s11030-013-9463-9
PMID:23907391
Abstract

The rhodium(II)-catalyzed reactions of cyclic diazo compounds derived from barbituric acid or thiobarbituric acid with arylacetylenes and styrenes were examined. These reactions provide a rapid synthetic route to the preparation of a variety of novel and diverse furo [2,3-d pyrimidine-2,4-diones, 2-thioxodihydrofuro [2,3-d pyrimidin-4-ones, dihydrofuro [2,3-d] pyrimidine-2,4-diones, and 2-thioxotetrahydrofuro [2,3-d] pyrimidin-4-ones.

摘要

研究了由巴比妥酸或硫代巴比妥酸衍生的环状重氮化合物与芳基乙炔和苯乙烯的铑(II)催化反应。这些反应为制备各种新型和多样的呋喃[2,3-d]嘧啶-2,4-二酮、2-硫代二氢呋喃[2,3-d]嘧啶-4-酮、二氢呋喃[2,3-d]嘧啶-2,4-二酮和 2-硫代四氢呋喃[2,3-d]嘧啶-4-酮提供了快速的合成途径。

相似文献

1
Efficient one-pot synthesis of novel and diverse furo[2,3-d] pyrimidinediones and thioxofuro[2,3-d] pyrimidineones by the rhodium (II) pivalate-catalyzed reactions of cyclic diazo compounds.通过铑(II)双(三氟甲磺酰基)亚胺催化的环状重氮化合物反应,高效一锅合成新型多样的呋喃并[2,3-d]嘧啶二酮和噻吩并[2,3-d]嘧啶酮。
Mol Divers. 2013 Nov;17(4):679-91. doi: 10.1007/s11030-013-9463-9. Epub 2013 Aug 2.
2
Direct Synthesis of 5-Aryl Barbituric Acids by Rhodium(II)-Catalyzed Reactions of Arenes with Diazo Compounds.铑(II)催化芳烃与重氮化合物反应直接合成5-芳基巴比妥酸
Angew Chem Int Ed Engl. 2015 Jun 15;54(25):7410-3. doi: 10.1002/anie.201502324. Epub 2015 May 8.
3
Synthesis of griseolic acid analogues: regioselective alpha-facial [1,2]-migration in the rhodium acetate catalyzed reaction of D-glucose derived alpha-diazo-beta-keto ester.灰黄霉素酸类似物的合成:在醋酸铑催化的D-葡萄糖衍生的α-重氮-β-酮酯反应中区域选择性的α-面[1,2]-迁移
J Org Chem. 2003 May 30;68(11):4531-4. doi: 10.1021/jo026858j.
4
A Novel and Efficient Five-Component Synthesis of Pyrazole Based Pyrido[2,3-d]pyrimidine-diones in Water: A Triply Green Synthesis.水中基于吡唑的吡啶并[2,3 - d]嘧啶二酮的新型高效五组分合成:三重绿色合成
Molecules. 2016 Apr 1;21(4):441. doi: 10.3390/molecules21040441.
5
Rh(III)-Catalyzed Direct Coupling of Azobenzenes with α-Diazo Esters: Facile Synthesis of Cinnolin-3(2H)-ones.铑(III)催化偶氮苯与α-重氮酯的直接偶联反应:简便合成噌啉-3(2H)-酮
Org Lett. 2015 Jun 5;17(11):2852-5. doi: 10.1021/acs.orglett.5b01298. Epub 2015 May 20.
6
Rhodium catalyzed arylation of diazo compounds with aryl boronic acids.铑催化重氮化合物与芳基硼酸的芳基化反应。
J Org Chem. 2015 Apr 3;80(7):3455-61. doi: 10.1021/jo502922r. Epub 2015 Mar 19.
7
Rhodium(II)-catalyzed cross-coupling of diazo compounds.铑(II)催化的重氮化合物交叉偶联反应。
Angew Chem Int Ed Engl. 2011 Mar 7;50(11):2544-8. doi: 10.1002/anie.201004923. Epub 2011 Feb 14.
8
New one-pot synthesis of spiro[furo[2,3-d]pyrimidine-6,5'-pyrimidine]pentaones and their sulfur analogues.新型一锅法合成螺[呋喃[2,3-d]嘧啶-6,5'-嘧啶]戊酮及其硫类似物。
Mol Divers. 2011 Aug;15(3):721-31. doi: 10.1007/s11030-011-9302-9. Epub 2011 Jan 29.
9
Three-Component Coupling of Aldehydes, 2-Aminopyridines, and Diazo Esters via Rhodium(III)-Catalyzed Imidoyl C-H Activation: Synthesis of Pyrido[1,2- a]pyrimidin-4-ones.通过铑(III)催化酰亚胺 C-H 活化的醛、2-氨基吡啶和重氮酯的三组分偶联反应:吡啶并[1,2-a]嘧啶-4-酮的合成。
Org Lett. 2019 Jun 7;21(11):3886-3890. doi: 10.1021/acs.orglett.9b00779. Epub 2019 Mar 21.
10
Mechanism of rhodium-catalyzed carbene formation from diazo compounds.铑催化重氮化合物形成卡宾的机理。
Org Lett. 2007 Apr 26;9(9):1663-5. doi: 10.1021/ol070345n. Epub 2007 Apr 5.

本文引用的文献

1
A spectral deciphering the perturbation of model transporter protein (HSA) by antibacterial pyrimidine derivative: pharmacokinetic and biophysical insights.光谱解析模型转运蛋白(HSA)受抗菌嘧啶衍生物的干扰:药代动力学和生物物理的见解。
J Photochem Photobiol B. 2013 Jan 5;118:1-8. doi: 10.1016/j.jphotobiol.2012.09.010. Epub 2012 Oct 27.
2
Synthesis and optimization of substituted furo[2,3-d]-pyrimidin-4-amines and 7H-pyrrolo[2,3-d]pyrimidin-4-amines as ACK1 inhibitors.取代的呋喃[2,3-d]-嘧啶-4-胺和 7H-吡咯并[2,3-d]嘧啶-4-胺的合成与优化作为 ACK1 抑制剂。
Bioorg Med Chem Lett. 2012 Oct 1;22(19):6212-7. doi: 10.1016/j.bmcl.2012.08.020. Epub 2012 Aug 10.
3
Rh-catalyzed intermolecular reactions of cyclic α-diazocarbonyl compounds with selectivity over tertiary C-H bond migration.
铑催化的环状α-重氮羰基化合物与选择性的叔 C-H 键迁移的分子间反应。
J Am Chem Soc. 2012 Jul 4;134(26):11035-43. doi: 10.1021/ja3046712. Epub 2012 Jun 19.
4
Highlights in the discovery of antiviral drugs: a personal retrospective.抗病毒药物发现历程中的亮点:个人回顾
J Med Chem. 2010 Feb 25;53(4):1438-50. doi: 10.1021/jm900932g.
5
Synthesis and EPR studies of 2'-deoxyuridines with alkynyl, rodlike linkages.具有炔基、棒状连接的2'-脱氧尿苷的合成与电子顺磁共振研究。
Chemistry. 2009 Aug 3;15(31):7569-77. doi: 10.1002/chem.200900481.
6
Diversity oriented syntheses of fused pyrimidines designed as potential antifolates.设计为潜在抗叶酸剂的稠合嘧啶的多样性导向合成。
Org Biomol Chem. 2009 May 7;7(9):1829-42. doi: 10.1039/b818339b. Epub 2009 Mar 6.
7
Antitumor activity of 6-(cyclohexylamino)-1, 3-dimethyl-5(2-pyridyl)furo[2,3-d]pyrimidine-2,4(1H,3H)-dione and Its Ti(IV), Zn(II), Fe(III), and Pd(II) complexes on K562 and Jurkat cell lines.6-(环己基氨基)-1,3-二甲基-5(2-吡啶基)呋喃[2,3-d]嘧啶-2,4(1H,3H)-二酮及其 Ti(IV)、Zn(II)、Fe(III)和 Pd(II)配合物对 K562 和 Jurkat 细胞系的抗肿瘤活性。
Bioinorg Chem Appl. 2008;2008:501021. doi: 10.1155/2008/501021. Epub 2009 Jan 26.
8
Zinc-catalyzed cycloisomerizations. Synthesis of substituted furans and furopyrimidine nucleosides.锌催化的环异构化反应。取代呋喃和呋喃嘧啶核苷的合成。
J Org Chem. 2008 Aug 1;73(15):5881-9. doi: 10.1021/jo8007995. Epub 2008 Jul 3.
9
Rational design of 4-amino-5,6-diaryl-furo[2,3-d]pyrimidines as potent glycogen synthase kinase-3 inhibitors.4-氨基-5,6-二芳基-呋喃并[2,3-d]嘧啶作为强效糖原合酶激酶-3抑制剂的合理设计
Bioorg Med Chem Lett. 2008 Mar 15;18(6):1967-71. doi: 10.1016/j.bmcl.2008.01.113. Epub 2008 Feb 2.
10
Synthesis and antiviral and cytostatic evaluations of the new C-5 substituted pyrimidine and furo[2,3-d]pyrimidine 4',5'-didehydro-L-ascorbic acid derivatives.新型C-5取代嘧啶和呋喃并[2,3-d]嘧啶4',5'-二脱氢-L-抗坏血酸衍生物的合成、抗病毒及细胞生长抑制活性评价
J Med Chem. 2007 Aug 23;50(17):4105-12. doi: 10.1021/jm070324z. Epub 2007 Aug 2.