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.
251 related articles for article (PubMed ID: 15754384)
1. Multicomponent domino processes based on the organocatalytic generation of conjugated acetylides: efficient synthetic manifolds for diversity-oriented molecular construction. Tejedor D; González-Cruz D; Santos-Expósito A; Marrero-Tellado JJ; de Armas P; García-Tellado F Chemistry; 2005 Jun; 11(12):3502-10. PubMed ID: 15754384 [TBL] [Abstract][Full Text] [Related]
2. Efficient domino process based on the catalytic generation of non-metalated, conjugated acetylides in the presence of aldehydes or activated ketones. Tejedor D; García-Tellado F; Marrero-Tellado JJ; de Armas P Chemistry; 2003 Jul; 9(13):3122-31. PubMed ID: 12833294 [TBL] [Abstract][Full Text] [Related]
3. A diversity-oriented strategy for the construction of tetrasubstituted pyrroles via coupled domino processes. Tejedor D; González-Cruz D; García-Tellado F; Marrero-Tellado JJ; Rodríguez ML J Am Chem Soc; 2004 Jul; 126(27):8390-1. PubMed ID: 15237991 [TBL] [Abstract][Full Text] [Related]
4. Acetylides from alkyl propiolates as building blocks for C3 homologation. Tejedor D; López-Tosco S; Cruz-Acosta F; Méndez-Abt G; García-Tellado F Angew Chem Int Ed Engl; 2009; 48(12):2090-8. PubMed ID: 19145618 [TBL] [Abstract][Full Text] [Related]
5. The development of catalytic nucleophilic additions of terminal alkynes in water. Li CJ Acc Chem Res; 2010 Apr; 43(4):581-90. PubMed ID: 20095650 [TBL] [Abstract][Full Text] [Related]
6. A substrate-based folding process incorporating chemodifferentiating ABB' three-component reactions of terminal alkynoates and 1,2-dicarbonyl compounds: a skeletal-diversity-oriented synthetic manifold. Tejedor D; Sántos-Expósito A; García-Tellado F Chemistry; 2007; 13(4):1201-9. PubMed ID: 17075926 [TBL] [Abstract][Full Text] [Related]
7. Propargyl Vinyl Ethers and Tertiary Skipped Diynes: Two Pluripotent Molecular Platforms for Diversity-Oriented Synthesis. Tejedor D; López-Tosco S; Méndez-Abt G; Cotos L; García-Tellado F Acc Chem Res; 2016 Apr; 49(4):703-13. PubMed ID: 27050293 [TBL] [Abstract][Full Text] [Related]
8. Metal-organic cooperative catalysis in C-H and C-C bond activation and its concurrent recovery. Park YJ; Park JW; Jun CH Acc Chem Res; 2008 Feb; 41(2):222-34. PubMed ID: 18247521 [TBL] [Abstract][Full Text] [Related]
11. Enantioselective reductive coupling of 1,3-enynes to heterocyclic aromatic aldehydes and ketones via rhodium-catalyzed asymmetric hydrogenation: mechanistic insight into the role of Brønsted acid additives. Komanduri V; Krische MJ J Am Chem Soc; 2006 Dec; 128(51):16448-9. PubMed ID: 17177363 [TBL] [Abstract][Full Text] [Related]
12. Catalytic metallonitrene/alkyne metathesis: a powerful cascade process for the synthesis of nitrogen-containing molecules. Thornton AR; Blakey SB J Am Chem Soc; 2008 Apr; 130(15):5020-1. PubMed ID: 18355007 [TBL] [Abstract][Full Text] [Related]
13. One-pot formation of chiral polysubstituted 3,4-dihydropyrans via a novel organocatalytic domino sequence involving alkynal self-condensation. Dong LJ; Fan TT; Wang C; Sun J Org Lett; 2013 Jan; 15(1):204-7. PubMed ID: 23259735 [TBL] [Abstract][Full Text] [Related]
14. Primary 1,2-diamine catalysis III: an unexpected domino reaction for the synthesis of multisubstituted cyclohexa-1,3-dienamines. Wang J; Li Q; Qi C; Liu Y; Ge Z; Li R Org Biomol Chem; 2010 Oct; 8(19):4240-2. PubMed ID: 20694251 [TBL] [Abstract][Full Text] [Related]
15. Organocatalytic sequential one-pot double cascade asymmetric synthesis of Wieland-Miescher ketone analogues from a Knoevenagel/hydrogenation/Robinson annulation sequence: scope and applications of organocatalytic biomimetic reductions. Ramachary DB; Kishor M J Org Chem; 2007 Jul; 72(14):5056-68. PubMed ID: 17552564 [TBL] [Abstract][Full Text] [Related]
16. Addition of alkynes to aldehydes and activated ketones catalyzed by rhodium-phosphine complexes. Dhondi PK; Carberry P; Choi LB; Chisholm JD J Org Chem; 2007 Dec; 72(25):9590-6. PubMed ID: 17999525 [TBL] [Abstract][Full Text] [Related]
17. Exploiting domino enyne metathesis mechanisms for skeletal diversity generation. Spandl RJ; Rudyk H; Spring DR Chem Commun (Camb); 2008 Jul; (26):3001-3. PubMed ID: 18688328 [TBL] [Abstract][Full Text] [Related]