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.
152 related articles for article (PubMed ID: 39076293)
21. Synthesis of a novel category of pseudo-peptides using an Ugi three-component reaction of levulinic acid as bifunctional substrate, amines, and amino acid-based isocyanides. Khalesi M; Ziyaei Halimehjani A; Martens J Beilstein J Org Chem; 2019; 15():852-857. PubMed ID: 31019577 [TBL] [Abstract][Full Text] [Related]
22. Formation of 1,1'-iminodicarboxylic acid derivatives, 2,6-diketo-piperazine and dibenzodiazocine-2,6-dione by variations of multicomponent reactions. Ugi IK; Ebert B; Hörl W Chemosphere; 2001 Apr; 43(1):75-81. PubMed ID: 11233828 [TBL] [Abstract][Full Text] [Related]
23. Multicomponent Ugi Reaction of Indole- N-carboxylic Acids: Expeditious Access to Indole Carboxamide Amino Amides. Zeng L; Sajiki H; Cui S Org Lett; 2019 Jul; 21(13):5269-5272. PubMed ID: 31247803 [TBL] [Abstract][Full Text] [Related]
24. Total Synthesis of Plusbacin A Katsuyama A; Yakushiji F; Ichikawa S J Org Chem; 2018 Jul; 83(13):7085-7101. PubMed ID: 29457732 [TBL] [Abstract][Full Text] [Related]
25. Applications of Convertible Isonitriles in the Ligation and Macrocyclization of Multicomponent Reaction-Derived Peptides and Depsipeptides. Wessjohann LA; Morejón MC; Ojeda GM; Rhoden CR; Rivera DG J Org Chem; 2016 Aug; 81(15):6535-45. PubMed ID: 27390908 [TBL] [Abstract][Full Text] [Related]
26. Synthesis of highly functionalized organic compounds through Ugi post-transformations started from propiolic acids. Mohammadi-Khanaposhtani M; Jalalimanesh N; Saeedi M; Larijani B; Mahdavi M Mol Divers; 2020 Aug; 24(3):855-887. PubMed ID: 31325081 [TBL] [Abstract][Full Text] [Related]
27. Cyclic Imines in Ugi and Ugi-Type Reactions. Nazeri MT; Farhid H; Mohammadian R; Shaabani A ACS Comb Sci; 2020 Aug; 22(8):361-400. PubMed ID: 32574488 [TBL] [Abstract][Full Text] [Related]
28. Ammonia-Promoted One-Pot Tetrazolopiperidinone Synthesis by Ugi Reaction. Patil P; Kurpiewska K; Kalinowska-Tłuścik J; Dömling A ACS Comb Sci; 2017 May; 19(5):343-350. PubMed ID: 28240545 [TBL] [Abstract][Full Text] [Related]
29. The new synthesis of pyrrole-fused dibenzo[ Nazeri MT; Ahmadi M; Ghasemi M; Shaabani A; Notash B Org Biomol Chem; 2023 May; 21(19):4095-4108. PubMed ID: 37128973 [TBL] [Abstract][Full Text] [Related]
30. Multicomponent synthesis of novel amino acid-nucleobase chimeras: a versatile approach to PNA-monomers. Maison W; Schlemminger I; Westerhoff O; Martens J Bioorg Med Chem; 2000 Jun; 8(6):1343-60. PubMed ID: 10896112 [TBL] [Abstract][Full Text] [Related]
31. An efficient and practical approach for the synthesis of indoloquinolines and indolo/pyrroloquinoxalines Iranfar S; Shiri M; Nosood YL; Keley ZA; Tanbakouchian Z; Amini Z; Al-Harrasi A; Hussain FHS RSC Adv; 2024 Jun; 14(26):18271-18276. PubMed ID: 38854840 [TBL] [Abstract][Full Text] [Related]
37. Recent Advances in the Synthesis of Peptidomimetics via Ugi Reactions. Liu C; Voskressensky LG; Van der Eycken EV Chemistry; 2024 Mar; 30(14):e202303597. PubMed ID: 38123521 [TBL] [Abstract][Full Text] [Related]
38. Using Triazolobenzodiazepine as the Cyclic Imine in Various Types of Joullié-Ugi Reactions. Nazeri MT; Ghasemi M; Ahmadi M; Shaabani A; Notash B J Org Chem; 2023 Oct; 88(19):13504-13519. PubMed ID: 37696794 [TBL] [Abstract][Full Text] [Related]
39. Asymmetric Ugi 3CR on isatin-derived ketimine: synthesis of chiral 3,3-disubstituted 3-aminooxindole derivatives. Lesma G; Meneghetti F; Sacchetti A; Stucchi M; Silvani A Beilstein J Org Chem; 2014; 10():1383-9. PubMed ID: 24991292 [TBL] [Abstract][Full Text] [Related]
40. A ligand-free Pd-catalyzed cascade reaction: an access to the highly diverse isoquinolin-1(2H)-one derivatives via isocyanide and Ugi-MCR synthesized amide precursors. Tyagi V; Khan S; Giri A; Gauniyal HM; Sridhar B; Chauhan PM Org Lett; 2012 Jun; 14(12):3126-9. PubMed ID: 22625424 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]