| Year |
Citation |
Score |
| 2023 |
Méndez Y, Vasco AV, Ebensen T, Schulze K, Yousefi M, Davari M, Wessjohann LA, Guzmán CA, Rivera DG, Westermann B. Diversification of a Novel α-Galactosyl Ceramide Hotspot Boosts the Adjuvant Properties in Parenteral and Mucosal Vaccines. Angewandte Chemie (International Ed. in English). e202310983. PMID 37857582 DOI: 10.1002/anie.202310983 |
0.41 |
|
| 2023 |
Vasco Vidal A, Mendez Y, González C, Perez C, Reguera L, Wessjohann L, Rivera DG. Advancing multicomponent strategies to macrobicyclic peptides. Chembiochem : a European Journal of Chemical Biology. e202300229. PMID 37171138 DOI: 10.1002/cbic.202300229 |
0.568 |
|
| 2022 |
Vasco AV, Ricardo MG, Rivera DG, Wessjohann LA. Ligation, Macrocyclization, and Simultaneous Functionalization of Peptides by Multicomponent Reactions (MCR). Methods in Molecular Biology (Clifton, N.J.). 2371: 143-157. PMID 34596847 DOI: 10.1007/978-1-0716-1689-5_8 |
0.571 |
|
| 2021 |
Fernandes VA, Lima RN, Broterson YB, Kawamura MY, Echemendía R, de la Torre AF, Ferreira MAB, Rivera DG, Paixão MW. Direct access to tetrasubstituted cyclopentenyl scaffolds through a diastereoselective isocyanide-based multicomponent reaction. Chemical Science. 12: 15862-15869. PMID 35024110 DOI: 10.1039/d1sc04158d |
0.643 |
|
| 2021 |
Ricardo MG, Vázquéz-Mena Y, Iglesias-Morales Y, Wessjohann LA, Rivera DG. On the scope of the double Ugi multicomponent stapling to produce helical peptides. Bioorganic Chemistry. 113: 104987. PMID 34022444 DOI: 10.1016/j.bioorg.2021.104987 |
0.563 |
|
| 2021 |
Rivera DG, Ricardo MG, Vasco AV, Wessjohann LA, Van der Eycken EV. On-resin multicomponent protocols for biopolymer assembly and derivatization. Nature Protocols. PMID 33473197 DOI: 10.1038/s41596-020-00445-6 |
0.712 |
|
| 2020 |
Reguera L, Cano A, Rodríguez-Hernández J, Rivera DG, Van der Eycken EV, Ramírez-Rosales D, Reguera E. CuCu and Ag-isocyanobenzoates as novel 1D semiconducting coordination oligomers. Dalton Transactions (Cambridge, England : 2003). PMID 32851997 DOI: 10.1039/d0dt02461a |
0.497 |
|
| 2020 |
Ojeda-Carralero GM, Ceballos LG, Coro J, Rivera DG. One Reacts as Two: Applications of N-isocyaniminotriphenylphosphorane in Diversity-Oriented Synthesis. Acs Combinatorial Science. PMID 32631055 DOI: 10.1021/Acscombsci.0C00111 |
0.485 |
|
| 2020 |
Rivera DG, Reguera L. Macrocyclic imino-peptides diversify to better target proteins. Chemmedchem. PMID 32516501 DOI: 10.1002/cmdc.202000261 |
0.362 |
|
| 2020 |
Vasco AV, Moya CG, Gröger S, Brandt W, Balbach J, Pérez CS, Wessjohann LA, Rivera DG. Insights into the secondary structures of lactam N-substituted stapled peptides. Organic & Biomolecular Chemistry. PMID 32400808 DOI: 10.1039/D0Ob00767F |
0.548 |
|
| 2020 |
Rivera DG, Ojeda-Carralero GM, Reguera L, Van der Eycken EV. Peptide macrocyclization by transition metal catalysis. Chemical Society Reviews. PMID 32142086 DOI: 10.1039/c9cs00366e |
0.625 |
|
| 2020 |
Vasco AV, Brode M, Méndez Y, Valdés O, Rivera DG, Wessjohann LA. Synthesis of Lactam-Bridged and Lipidated Cyclo-Peptides as Promising Anti-Phytopathogenic Agents. Molecules (Basel, Switzerland). 25. PMID 32069902 DOI: 10.3390/Molecules25040811 |
0.537 |
|
| 2020 |
Doemling A, Ricardo M, Ali A, Plewka J, Surmiak E, Labuzek B, Neochoritis C, Atmaj J, Skalniak L, Zhang R, Holak T, Groves M, Rivera D. Multicomponent Peptide Stapling as a Diversity-Driven Tool for the Development of Inhibitors of Protein-Protein Interactions. Angewandte Chemie (International Ed. in English). PMID 31944488 DOI: 10.2210/Pdb6T2F/Pdb |
0.445 |
|
| 2019 |
Ricardo MG, Moya CG, Pérez CS, Porzel A, Wessjohann LA, Rivera DG. Improved Stability and Tunable Functionalization of Parallel β-Sheets via Multicomponent N-Alkylation of the Turn Moiety. Angewandte Chemie (International Ed. in English). PMID 31797518 DOI: 10.1002/Anie.201912095 |
0.604 |
|
| 2019 |
Vicente FEM, González-Garcia M, Diaz Pico E, Moreno-Castillo E, Garay HE, Rosi PE, Jimenez AM, Campos-Delgado JA, Rivera DG, Chinea G, Pietro RCLR, Stenger S, Spellerberg B, Kubiczek D, Bodenberger N, et al. Design of a Helical-Stabilized, Cyclic, and Nontoxic Analogue of the Peptide Cm-p5 with Improved Antifungal Activity. Acs Omega. 4: 19081-19095. PMID 31763531 DOI: 10.1021/acsomega.9b02201 |
0.579 |
|
| 2019 |
Ojeda GM, Ranjan P, Fedoseev P, Amable L, Sharma UK, Rivera DG, Van der Eycken EV. Combining the Ugi-azide multicomponent reaction and rhodium(III)-catalyzed annulation for the synthesis of tetrazole-isoquinolone/pyridone hybrids. Beilstein Journal of Organic Chemistry. 15: 2447-2457. PMID 31666879 DOI: 10.3762/bjoc.15.237 |
0.621 |
|
| 2019 |
Ricardo MG, Vasco AV, Rivera DG, Wessjohann LA. Stabilization of Cyclic β-Hairpins by Ugi-Reaction-Derived -Alkylated Peptides: The Quest for Functionalized β-Turns. Organic Letters. PMID 31482710 DOI: 10.1021/Acs.Orglett.9B02592 |
0.505 |
|
| 2019 |
Reguera L, Attorresi CI, Ramírez JA, Rivera DG. Steroid diversification by multicomponent reactions. Beilstein Journal of Organic Chemistry. 15: 1236-1256. PMID 31293671 DOI: 10.3762/bjoc.15.121 |
0.406 |
|
| 2019 |
de la Torre AF, Scatena GS, Valdés O, Rivera DG, Paixão MW. Ugi reaction-derived prolyl peptide catalysts grafted on the renewable polymer polyfurfuryl alcohol for applications in heterogeneous enamine catalysis. Beilstein Journal of Organic Chemistry. 15: 1210-1216. PMID 31293668 DOI: 10.3762/Bjoc.15.118 |
0.591 |
|
| 2019 |
Reguera L, Rivera DG. Multicomponent Reaction Toolbox for Peptide Macrocyclization and Stapling. Chemical Reviews. PMID 30990310 DOI: 10.1021/acs.chemrev.8b00744 |
0.416 |
|
| 2018 |
Ricardo MG, Llanes D, Wessjohann LA, Rivera DG. Introducing the Petasis Reaction for Late-Stage Multicomponent Diversification, Labeling, and Stapling of Peptides. Angewandte Chemie (International Ed. in English). PMID 30589179 DOI: 10.1002/Anie.201812620 |
0.591 |
|
| 2018 |
Vasco AV, Mendez Y, Porzel A, Balbach J, Wessjohann LA, Rivera DG. A Multicomponent Stapling Approach to Exocyclic Functionalized Helical Pep-tides: Adding Lipids, Sugar, PEGs, Labels and Handles to the Lactam Bridge. Bioconjugate Chemistry. PMID 30575393 DOI: 10.1021/Acs.Bioconjchem.8B00906 |
0.598 |
|
| 2018 |
Ricardo MG, Marrero JF, Valdes O, Rivera DG, Wessjohann LA. A Peptide Backbone Stapling Strategy Enabled by the Multicomponent Incorporation of Amide N-Substituents. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30412333 DOI: 10.1002/Chem.201805318 |
0.617 |
|
| 2018 |
Echemendía R, da Silva GP, Kawamura MY, de la Torre AF, Corrêa AG, Ferreira MAB, Rivera DG, Paixão MW. A stereoselective sequential organocascade and multicomponent approach for the preparation of tetrahydropyridines and chimeric derivatives. Chemical Communications (Cambridge, England). PMID 30411110 DOI: 10.1039/C8Cc06871B |
0.647 |
|
| 2018 |
Ravanello BB, Seixas N, Rodrigues OED, da Silva RS, Villetti MA, Frolov A, Rivera DG, Westermann B. Diversity Driven Decoration and Ligation of Fullerene by Ugi and Passerini Multicomponent Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29882608 DOI: 10.1002/chem.201802414 |
0.402 |
|
| 2018 |
Reguera L, Méndez Y, Humpierre AR, Valdés O, Rivera DG. Multicomponent Reactions in Ligation and Bioconjugation Chemistry. Accounts of Chemical Research. PMID 29799718 DOI: 10.1021/acs.accounts.8b00126 |
0.394 |
|
| 2018 |
Méndez Y, Chang J, Humpierre AR, Zanuy A, Garrido R, Vasco AV, Pedroso J, Santana D, Rodríguez LM, García-Rivera D, Valdés Y, Vérez-Bencomo V, Rivera DG. Multicomponent polysaccharide-protein bioconjugation in the development of antibacterial glycoconjugate vaccine candidates. Chemical Science. 9: 2581-2588. PMID 29719713 DOI: 10.1039/C7Sc05467J |
0.304 |
|
| 2017 |
Puentes AR, Morejón MC, Rivera DG, Wessjohann LA. Peptide Macrocyclization Assisted by Traceless Turn Inducers Derived from Ugi Peptide Ligation with Cleavable and Resin-Linked Amines. Organic Letters. PMID 28704057 DOI: 10.1021/Acs.Orglett.7B01761 |
0.591 |
|
| 2017 |
Morejón MC, Laub A, Kaluđerović GN, Puentes AR, Hmedat AN, Otero-González AJ, Rivera DG, Wessjohann LA. A multicomponent macrocyclization strategy to natural product-like cyclic lipopeptides: synthesis and anticancer evaluation of surfactin and mycosubtilin analogues. Organic & Biomolecular Chemistry. PMID 28406518 DOI: 10.1039/C7Ob00459A |
0.592 |
|
| 2017 |
Wessjohann LA, Kreye O, Rivera DG. One-Pot Assembly of Amino Acid Bridged Hybrid Macromulticyclic Cages through Multiple Multicomponent Macrocyclizations. Angewandte Chemie (International Ed. in English). PMID 28211208 DOI: 10.1002/Anie.201610801 |
0.616 |
|
| 2017 |
Rivera D, Wessjohann L, Puentes A, Neves Filho R. Total Synthesis of Cordyheptapeptide A Synlett. 28: 1971-1974. DOI: 10.1055/S-0036-1588433 |
0.625 |
|
| 2017 |
Jorge EYC, Lima TdM, Lima CGS, Marchini L, Castelblanco WN, Rivera DG, Urquieta-González EA, Varma RS, Paixão MW. Metal-exchanged magnetic β-zeolites: valorization of lignocellulosic biomass-derived compounds to platform chemicals Green Chemistry. 19: 3856-3868. DOI: 10.1039/C7Gc01178D |
0.574 |
|
| 2017 |
Echemendía R, Fernández O, Coro J, Suárez M, Rivera DG. A versatile approach to hybrid thiadiazine-based molecules by the Ugi four-component reaction Tetrahedron Letters. 58: 1784-1787. DOI: 10.1016/J.Tetlet.2017.03.075 |
0.48 |
|
| 2016 |
Morejón MC, Laub A, Westermann B, Rivera DG, Wessjohann LA. Solution- and Solid-Phase Macrocyclization of Peptides by the Ugi-Smiles Multicomponent Reaction: Synthesis of N-Aryl-Bridged Cyclic Lipopeptides. Organic Letters. PMID 27505031 DOI: 10.1021/Acs.Orglett.6B02001 |
0.646 |
|
| 2016 |
Wessjohann LA, Morejón MC, Ojeda Carralero GM, Bohn-Rhoden CR, Rivera DG. Applications of Convertible Isonitriles in the Ligation and Macrocyclization of Multicomponent Reaction-Derived Peptides and Depsipeptides. The Journal of Organic Chemistry. PMID 27390908 DOI: 10.1021/Acs.Joc.6B01150 |
0.628 |
|
| 2016 |
de la Torre AF, Rivera DG, Concepción O, Echemendia R, Correa AG, Paixão MW. Multicomponent Synthesis of Cyclic Depsipeptide Mimics by Ugi Reaction Including Cyclic Hemiacetals Derived from Asymmetric Organocatalysis. The Journal of Organic Chemistry. 81: 803-9. PMID 26720907 DOI: 10.1021/Acs.Joc.5B02158 |
0.693 |
|
| 2016 |
De La Torre AF, Rivera DG, Concepción O, Echemendia R, Correa AG, Paixão MW. Multicomponent synthesis of cyclic depsipeptide mimics by Ugi reaction including cyclic hemiacetals derived from asymmetric organocatalysis Journal of Organic Chemistry. 81: 803-809. DOI: 10.1021/acs.joc.5b02158 |
0.41 |
|
| 2015 |
Vasco AV, Pérez CS, Morales FE, Garay HE, Vasilev D, Gavín JA, Wessjohann LA, Rivera DG. Macrocyclization of Peptide Side Chains by the Ugi Reaction: Achieving Peptide Folding and Exocyclic N-Functionalization in One Shot. The Journal of Organic Chemistry. 80: 6697-707. PMID 26030840 DOI: 10.1021/Acs.Joc.5B00858 |
0.615 |
|
| 2015 |
Morales FE, Garay HE, Muñoz DF, Augusto YE, Otero-González AJ, Reyes Acosta O, Rivera DG. Aminocatalysis-Mediated on-Resin Ugi Reactions: Application in the Solid-Phase Synthesis of N-Substituted and Tetrazolo Lipopeptides and Peptidosteroids. Organic Letters. 17: 2728-31. PMID 25994574 DOI: 10.1021/Acs.Orglett.5B01147 |
0.491 |
|
| 2015 |
Echemendía R, De La Torre AF, Monteiro JL, Pila M, Corrêa AG, Westermann B, Rivera DG, Paixão MW. Highly stereoselective synthesis of natural-product-like hybrids by an organocatalytic/multicomponent reaction sequence Angewandte Chemie - International Edition. 54: 7621-7625. PMID 25967546 DOI: 10.1002/Anie.201412074 |
0.699 |
|
| 2015 |
Ricardo MG, Morales FE, Garay H, Reyes O, Vasilev D, Wessjohann LA, Rivera DG. Bidirectional macrocyclization of peptides by double multicomponent reactions. Organic & Biomolecular Chemistry. 13: 438-46. PMID 25371987 DOI: 10.1039/C4Ob01915F |
0.653 |
|
| 2014 |
Rivera DG, Vasco AV, Echemendía R, Concepción O, Pérez CS, Gavín JA, Wessjohann LA. A multicomponent conjugation strategy to unique N-steroidal peptides: first evidence of the steroidal nucleus as a β-turn inducer in acyclic peptides. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 13150-61. PMID 25212273 DOI: 10.1002/Chem.201403773 |
0.613 |
|
| 2014 |
Méndez Y, Pérez-Labrada K, González-Bacerio J, Valdés G, de los Chávez MÁ, Osuna J, Charli JL, Pascual I, Rivera DG. Combinatorial multicomponent access to natural-products-inspired peptidomimetics: discovery of selective inhibitors of microbial metallo-aminopeptidases. Chemmedchem. 9: 2351-9. PMID 24989844 DOI: 10.1002/Cmdc.201402140 |
0.333 |
|
| 2014 |
Pérez‐Labrada K, Brouard I, Méndez I, Pérez CS, Gavín JA, Rivera DG. Combined Ugi‐4CR/CuAAC Approach to Triazole‐Based Neoglycolipids European Journal of Organic Chemistry. 2014: 3671-3683. DOI: 10.1002/Ejoc.201402117 |
0.445 |
|
| 2014 |
Scatena GS, De La Torre AF, Cass QB, Rivera DG, Paixão MW. Multicomponent approach to silica-grafted peptide catalysts: A 3D continuous-flow organocatalytic system with on-line monitoring of conversion and stereoselectivity Chemcatchem. 6: 3208-3214. DOI: 10.1002/Cctc.201402501 |
0.648 |
|
| 2013 |
de la Torre AF, Rivera DG, Ferreira MA, Corrêa AG, Paixão MW. Multicomponent combinatorial development and conformational analysis of prolyl peptide-peptoid hybrid catalysts: application in the direct asymmetric Michael addition. The Journal of Organic Chemistry. 78: 10221-32. PMID 24053491 DOI: 10.1021/Jo401609Z |
0.656 |
|
| 2013 |
Pérez-Labrada K, Méndez Y, Brouard I, Rivera DG. Multicomponent ligation of steroids: creating diversity at the linkage moiety of bis-spirostanic conjugates by Ugi reactions. Acs Combinatorial Science. 15: 320-30. PMID 23573787 DOI: 10.1021/Co400028E |
0.525 |
|
| 2013 |
Rivera DG, León F, Concepción O, Morales FE, Wessjohann LA. A multiple multicomponent approach to chimeric peptide-peptoid podands. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 6417-28. PMID 23512744 DOI: 10.1002/Chem.201201591 |
0.631 |
|
| 2013 |
Pérez-Labrada K, Morera C, Brouard I, Llerena R, Rivera DG. Synthesis and conformational study of triazole-linked bis-spirostanic conjugates Tetrahedron Letters. 54: 1602-1606. DOI: 10.1016/J.Tetlet.2013.01.058 |
0.484 |
|
| 2013 |
Narayanaperumal S, Rivera DG, Silva RC, Paixão MW. Terpene-Derived Bifunctional Thioureas in Asymmetric Organocatalysis Chemcatchem. 5: 2756-2773. DOI: 10.1002/Cctc.201200936 |
0.637 |
|
| 2012 |
Rivera DG, Pérez-Labrada K, Lambert L, Dörner S, Westermann B, Wessjohann LA. Carbohydrate-steroid conjugation by Ugi reaction: one-pot synthesis of triple sugar/pseudo-peptide/spirostane hybrids. Carbohydrate Research. 359: 102-10. PMID 22925772 DOI: 10.1016/J.Carres.2012.05.003 |
0.666 |
|
| 2012 |
Deobald AM, Corrêa AG, Rivera DG, Paixão MW. Organocatalytic asymmetric epoxidation and tandem epoxidation/Passerini reaction under eco-friendly reaction conditions. Organic & Biomolecular Chemistry. 10: 7681-4. PMID 22918441 DOI: 10.1039/C2Ob26247A |
0.664 |
|
| 2012 |
Pérez-Labrada K, Brouard I, Estévez S, Marrero MT, Estévez F, Rivera DG. Effect of C-ring modifications on the cytotoxicity of spirostan saponins and related glycosides. Bioorganic & Medicinal Chemistry. 20: 4522-31. PMID 22682921 DOI: 10.1016/J.Bmc.2012.05.018 |
0.321 |
|
| 2012 |
Pérez-Labrada K, Brouard I, Méndez I, Rivera DG. Multicomponent synthesis of Ugi-type ceramide analogues and neoglycolipids from lipidic isocyanides. The Journal of Organic Chemistry. 77: 4660-70. PMID 22533639 DOI: 10.1021/Jo300462M |
0.414 |
|
| 2012 |
Pérez-Labrada K, Brouard I, Estévez S, Marrero MT, Estévez F, Bermejo J, Rivera DG. New insights into the structure-cytotoxicity relationship of spirostan saponins and related glycosides. Bioorganic & Medicinal Chemistry. 20: 2690-700. PMID 22405922 DOI: 10.1016/J.Bmc.2012.02.026 |
0.337 |
|
| 2011 |
Pérez-Labrada K, Flórez-López E, Paz-Morales E, Miranda LD, Rivera DG. A two-step practical synthesis of dehydroalanine derivatives Tetrahedron Letters. 52: 1635-1638. DOI: 10.1016/J.Tetlet.2011.01.122 |
0.426 |
|
| 2011 |
Pérez-Labrada K, Brouard I, Morera C, Estévez F, Bermejo J, Rivera DG. 'Click' synthesis of triazole-based spirostan saponin analogs Tetrahedron. 67: 7713-7727. DOI: 10.1016/J.Tet.2011.08.003 |
0.437 |
|
| 2009 |
Rhoden CR, Rivera DG, Kreye O, Bauer AK, Westermann B, Wessjohann LA. Rapid access to N-substituted diketopiperazines by one-pot Ugi-4CR/deprotection+activation/cyclization (UDAC). Journal of Combinatorial Chemistry. 11: 1078-82. PMID 19795905 DOI: 10.1021/Cc900106U |
0.623 |
|
| 2009 |
Rivera DG, Wessjohann LA. Architectural chemistry: Synthesis of topologically diverse macromulticycles by sequential multiple multicomponent macrocyclizations Journal of the American Chemical Society. 131: 3721-3732. PMID 19275261 DOI: 10.1021/Ja809005K |
0.608 |
|
| 2009 |
Wessjohann LA, Rivera DG, Vercillo OE. Multiple multicomponent macrocyclizations (MiBs): a strategic development toward macrocycle diversity. Chemical Reviews. 109: 796-814. PMID 19166290 DOI: 10.1021/Cr8003407 |
0.741 |
|
| 2009 |
Coro J, RodrÃguez H, Rivera DG, Suárez M, Molero D, Herranz MÃ, MartÃnez-Ãlvarez R, Filippone S, MartÃn N. Functional Chimeras: New BingelâHirsch-Type SteroidâFullerene Hybrids European Journal of Organic Chemistry. 2009: 4810-4817. DOI: 10.1002/Ejoc.200900583 |
0.368 |
|
| 2008 |
Rivera DG, Pando O, Bosch R, Wessjohann LA. A biomimetic approach for polyfunctional secocholanes: tuning flexibility and functionality on peptidic and macrocyclic scaffolds derived from bile acids. The Journal of Organic Chemistry. 73: 6229-38. PMID 18642868 DOI: 10.1021/Jo800708M |
0.631 |
|
| 2008 |
Rivera DG, Vercillo OE, Wessjohann LA. Rapid generation of macrocycles with natural-product-like side chains by multiple multicomponent macrocyclizations (MiBs). Organic & Biomolecular Chemistry. 6: 1787-95. PMID 18452014 DOI: 10.1039/B715393G |
0.741 |
|
| 2008 |
Leon F, Rivera DG, Wessjohann LA. Multiple multicomponent macrocyclizations including bifunctional building blocks (MiBs) based on Staudinger and Passerini three-component reactions. The Journal of Organic Chemistry. 73: 1762-7. PMID 18247489 DOI: 10.1021/Jo7022125 |
0.556 |
|
| 2008 |
Rivera DG, Concepción O, Pérez-Labrada K, Coll F. Synthesis of diamino-furostan sapogenins and their use as scaffolds for positioning peptides in a preorganized form Tetrahedron. 64: 5298-5305. DOI: 10.1016/J.Tet.2008.03.023 |
0.512 |
|
| 2008 |
Wessjohann LA, Andrade CKZ, Vercillo OE, Rivera DG. ChemInform Abstract: Macrocyclic Peptoids: N-Alkylated Cyclopeptides and Depsipeptides Cheminform. 39. DOI: 10.1002/CHIN.200834259 |
0.42 |
|
| 2007 |
Rivera DG, Wessjohann LA. Synthesis of novel steroid-peptoid hybrid macrocycles by multiple multicomponent macrocyclizations including bifunctional building blocks (MiBs) Molecules. 12: 1890-1899. PMID 17960094 DOI: 10.3390/12081890 |
0.614 |
|
| 2007 |
Wessjohann LA, Rivera DG, León F. Freezing imine exchange in dynamic combinatorial libraries with Ugi reactions: versatile access to templated macrocycles. Organic Letters. 9: 4733-6. PMID 17924638 DOI: 10.1021/Ol7021033 |
0.566 |
|
| 2007 |
Rivera DG, Pando O, Suardiaz R, Coll F. Studies on the regioselectivity of the Baeyer-Villiger reaction of 3-keto steroids: conformational effects determine the migration aptitude. Steroids. 72: 466-73. PMID 17412379 DOI: 10.1016/J.Steroids.2007.01.002 |
0.34 |
|
| 2007 |
Wessjohann LA, Rivera DG, Coll F. Synthesis of steroid-biaryl ether hybrid macrocycles with high skeletal and side chain variability by multiple multicomponent macrocyclization including bifunctional building blocks. The Journal of Organic Chemistry. 71: 7521-6. PMID 16995654 DOI: 10.1021/Jo0608570 |
0.606 |
|
| 2007 |
Wessjohann L, Rivera D, Vercillo O. Combinatorial Synthesis of Macrocycles by Multiple Multicomponent Macrocyclization Including Bifunctional Building Blocks (MiB) Synlett. 2007: 0308-0312. DOI: 10.1055/S-2007-968006 |
0.58 |
|
| 2006 |
Rivera DG, Wessjohann LA. Supramolecular compounds from multiple ugi multicomponent macrocyclizations: Peptoid-based cryptands, cages, and cryptophanes Journal of the American Chemical Society. 128: 7122-7123. PMID 16734440 DOI: 10.1021/Ja060720R |
0.573 |
|
| 2006 |
Wessjohann LA, Voigt B, Rivera DG. Diversity oriented one-pot synthesis of complex macrocycles: very large steroid-peptoid hybrids from multiple multicomponent reactions including bifunctional building blocks. Angewandte Chemie (International Ed. in English). 44: 4785-90. PMID 15988773 DOI: 10.1002/Anie.200500019 |
0.57 |
|
| 2006 |
Perez C, Leliebre-Lara V, Concepcion O, Coll F, Rivera D, Pando O. Synthesis and Biological Evaluation of Spirostanes Including Butyrolactone Moieties Letters in Organic Chemistry. 3: 519-522. DOI: 10.2174/157017806778341870 |
0.369 |
|
| 2006 |
Rivera DG, Pando O, Coll F. Synthesis of peptidomimetic-spirostane hybrids via Ugi reaction: a versatile approach for the formation of peptide–steroid conjugates Tetrahedron. 62: 8327-8334. DOI: 10.1016/J.Tet.2006.06.050 |
0.493 |
|
| 2006 |
Kreye O, Westermann B, Rivera DG, Johnson DV, Orru RVA, Wessjohann LA. Dye-modified and photoswitchable macrocycles by multiple multicomponent macrocyclizations including bifunctional building blocks (MiBs) Qsar and Combinatorial Science. 25: 461-464. DOI: 10.1002/Qsar.200540217 |
0.529 |
|
| 2005 |
Rivera DG, Coll F. Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds Canadian Journal of Chemistry. 83: 1084-1092. DOI: 10.1139/V05-051 |
0.352 |
|
| 2004 |
Rivera DG, Pando O, Leliebre-Lara V, Coll D, Leon F, Coll F. Synthesis of Spirostanic Analogues of Brassinosteroids via Homogeneous Permanganate Dihydroxylation. Cheminform. 35. DOI: 10.3184/030823404323000783 |
0.341 |
|
| 2003 |
Rivera D, Peseke K, Jomarrón I, Montero A, Molina R, Coll F. Synthesis of New Pyrazole and Pyrimidine Steroidal Derivatives Molecules. 8: 444-452. DOI: 10.3390/80500444 |
0.34 |
|
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