These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
154 related articles for article (PubMed ID: 35480285)
1. Activator free diastereoselective 1,3-dipolar cycloaddition: a quick access to coumarin based spiro multi heterocyclic adducts. Thadem N; Rajesh M; Das S RSC Adv; 2021 Sep; 11(48):29934-29938. PubMed ID: 35480285 [TBL] [Abstract][Full Text] [Related]
3. Heterogeneous graphene oxide as recyclable catalyst for azomethine ylide mediated 1,3 dipolar cycloaddition reaction in aqueous medium. Reddy MS; Kumar NS; Chowhan LR RSC Adv; 2018 Oct; 8(62):35587-35593. PubMed ID: 35547897 [TBL] [Abstract][Full Text] [Related]
4. Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines through Azomethine Ylide Cycloaddition Reaction. Haddad S; Boudriga S; Porzio F; Soldera A; Askri M; Knorr M; Rousselin Y; Kubicki MM; Golz C; Strohmann C J Org Chem; 2015 Sep; 80(18):9064-75. PubMed ID: 26291879 [TBL] [Abstract][Full Text] [Related]
5. A Facile One-Pot Construction of Succinimide-Fused Spiro[Pyrrolidine-2,3'-Oxindoles] via 1,3-Dipolar Cycloaddition Involving 3-Amino Oxindoles and Maleimides. Jin L; Liang F Molecules; 2018 Mar; 23(3):. PubMed ID: 29510590 [TBL] [Abstract][Full Text] [Related]
6. 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides with Carbonyl Dipolarophiles Yielding Oxazolidine Derivatives. Meyer AG; Ryan JH Molecules; 2016 Jul; 21(8):. PubMed ID: 27455230 [TBL] [Abstract][Full Text] [Related]
7. Azomethine ylide cycloaddition: a versatile tool for preparing novel pyrrolizidino-spiro-oxindolo hybrids of the doubly conjugated alkamide piperine. Singh M; Amrutha Krishnan AV; Mandal R; Samanta J; Ravichandiran V; Natarajan R; Bharitkar YP; Hazra A Mol Divers; 2020 Aug; 24(3):627-639. PubMed ID: 31183672 [TBL] [Abstract][Full Text] [Related]
8. Theoretical Study of the Mechanism of the Formation of Azomethine Ylide from Isatine and Sarcosine and Its Reactivity in 1,3-Dipolar Cycloaddition Reaction with 7-Oxabenzonorbornadiene. Antol I; Štrbac P; Murata Y; Margetić D Int J Mol Sci; 2024 Jun; 25(12):. PubMed ID: 38928235 [TBL] [Abstract][Full Text] [Related]
9. Diastereoselective synthesis of indolenine-based spiro[pyrazolone-4,2'-pyrrolidine] scaffolds via 1,3-dipolar cycloaddition of 4-aminopyrazolones, aldehydes, and indolenines. Nawaz S; Wei S; Huang Y; Wang W; Qu J; Wang B Org Biomol Chem; 2021 Aug; 19(32):6964-6968. PubMed ID: 34333584 [TBL] [Abstract][Full Text] [Related]
10. Catalytic enantioselective 1,3-dipolar cycloadditions of azomethine ylides for biology-oriented synthesis. Narayan R; Potowski M; Jia ZJ; Antonchick AP; Waldmann H Acc Chem Res; 2014 Apr; 47(4):1296-310. PubMed ID: 24730692 [TBL] [Abstract][Full Text] [Related]
11. 1,3-Dipolar cycloaddition reactions of isatin-derived azomethine ylides for the synthesis of spirooxindole and indole-derived scaffolds: recent developments. Miankooshki FR; Bayat M; Nasri S; Samet NH Mol Divers; 2023 Oct; 27(5):2365-2397. PubMed ID: 35925529 [TBL] [Abstract][Full Text] [Related]
12. The [3 + 3]-cycloaddition alternative for heterocycle syntheses: catalytically generated metalloenolcarbenes as dipolar adducts. Xu X; Doyle MP Acc Chem Res; 2014 Apr; 47(4):1396-405. PubMed ID: 24650430 [TBL] [Abstract][Full Text] [Related]
13. A facile synthesis of functionalized dispirooxindole derivatives via a three-component 1,3-dipolar cycloaddition reaction. He J; Ouyang G; Yuan Z; Tong R; Shi J; Ouyang L Molecules; 2013 May; 18(5):5142-54. PubMed ID: 23644979 [TBL] [Abstract][Full Text] [Related]
14. Graphene Oxide Catalyzed Synthesis of Fused Chromeno Spiro Pyrrolidine Oxindoles Singh V; Lakshmi SR; Chowhan LR Front Chem; 2021; 9():759436. PubMed ID: 35087791 [TBL] [Abstract][Full Text] [Related]
15. Decarboxylative 1,3-dipolar cycloaddition of amino acids for the synthesis of heterocyclic compounds. Zhang X; Ma X; Zhang W Beilstein J Org Chem; 2023; 19():1677-1693. PubMed ID: 38025085 [TBL] [Abstract][Full Text] [Related]
16. [Bmim]Br Accelerated One-Pot Three-Component Cascade Protocol for the Construction of Spirooxindole-Pyrrolidine Heterocyclic Hybrids. Kumar RS; M Al-Thamili D; Almansour AI; Arumugam N; Dege N Molecules; 2020 Oct; 25(20):. PubMed ID: 33080968 [TBL] [Abstract][Full Text] [Related]
17. An Expedient Regio- and Diastereoselective Synthesis of Hybrid Frameworks with Embedded Spiro[9,10]dihydroanthracene [9,3']-pyrrolidine and Spiro[oxindole-3,2'-pyrrolidine] Motifs via an Ionic Liquid-Mediated Multicomponent Reaction. Arumugam N; Almansour AI; Kumar RS; Menéndez JC; Sultan MA; Karama U; Ghabbour HA; Fun HK Molecules; 2015 Sep; 20(9):16142-53. PubMed ID: 26404224 [TBL] [Abstract][Full Text] [Related]
18. Engaging Isatins and Amino Acids in Multicomponent One-Pot 1,3-Dipolar Cycloaddition Reactions-Easy Access to Structural Diversity. Zhao H; Zhao Y Molecules; 2023 Sep; 28(18):. PubMed ID: 37764264 [TBL] [Abstract][Full Text] [Related]
19. Synthesis of pyrrolo(spiro-[2.3']-oxindole)-spiro-[4.3"]-oxindole via 1,3-dipolar cycloaddition of azomethine ylides with 3-acetonylideneoxindole. Xiao JA; Zhang HG; Liang S; Ren JW; Yang H; Chen XQ J Org Chem; 2013 Nov; 78(22):11577-83. PubMed ID: 24111532 [TBL] [Abstract][Full Text] [Related]
20. Dipolarophile-Controlled Regioselective 1,3-Dipolar Cycloaddition: A Switchable Divergent Access to Functionalized Wang Y; Yan L; Yan Y; Li S; Lu H; Liu J; Dong J Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36835183 [No Abstract] [Full Text] [Related] [Next] [New Search]