| Year |
Citation |
Score |
| 2023 |
Noleto-Dias C, Farag MA, Porzel A, Tavares JF, Wessjohann LA. A multiplex approach of MS, 1D-, and 2D-NMR metabolomics in plant ontogeny: A case study on Clusia minor L. organs (leaf, flower, fruit, and seed). Phytochemical Analysis : Pca. PMID 38069552 DOI: 10.1002/pca.3300 |
0.406 |
|
| 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 |
0.51 |
|
| 2023 |
Nugraha AS, Firli LN, Rani DM, Hidayatiningsih A, Lestari ND, Wongso H, Tarman K, Rahaweman AC, Manurung J, Ariantari NP, Papu A, Putra MY, Pratama ANW, Wessjohann LA, Keller PA. Indonesian marine and its medicinal contribution. Natural Products and Bioprospecting. 13: 38. PMID 37843645 DOI: 10.1007/s13659-023-00403-1 |
0.721 |
|
| 2023 |
Farag MA, Baky MH, Morgan I, Khalifa MR, Rennert R, Mohamed OG, El-Sayed MM, Porzel A, Wessjohann LA, Ramadan NS. Comparison of parts: metabolome providing insights into plant health benefits and valorization purposes as analyzed using multiplex GC-MS, LC-MS, NMR-based metabolomics, and molecular networking. Rsc Advances. 13: 21471-21493. PMID 37485437 DOI: 10.1039/d3ra03141a |
0.467 |
|
| 2023 |
Lam YTH, Hoppe J, Dang QN, Porzel A, Soboleva A, Brandt W, Rennert R, Hussain H, Davari MD, Wessjohann L, Arnold N. Purpurascenines A-C, Azepino-Indole Alkaloids from : Isolation, Biosynthesis, and Activity Studies on the 5-HT Receptor. Journal of Natural Products. 86: 1373-1384. PMID 37306303 DOI: 10.1021/acs.jnatprod.2c00716 |
0.515 |
|
| 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 |
0.538 |
|
| 2023 |
Noleto-Dias C, Picoli EAT, Porzel A, Wessjohann LA, Tavares JF, Farag MA. Metabolomics characterizes early metabolic changes and markers of tolerant Eucalyptus ssp. clones against drought stress. Phytochemistry. 212: 113715. PMID 37156433 DOI: 10.1016/j.phytochem.2023.113715 |
0.425 |
|
| 2023 |
Otify AM, Ibrahim RM, Abib B, Laub A, Wessjohann LA, Jiang Y, Farag MA. Unveiling metabolome heterogeneity and new chemicals in 7 tomato varieties via multiplex approach of UHPLC-MS/MS, GC-MS, and UV-Vis in relation to antioxidant effects as analyzed using molecular networking and chemometrics. Food Chemistry. 417: 135866. PMID 36913868 DOI: 10.1016/j.foodchem.2023.135866 |
0.421 |
|
| 2022 |
Abdel Shakour ZT, El-Akad RH, Elshamy AI, El Gendy AEG, Wessjohann LA, Farag MA. Dissection of Moringa oleifera leaf metabolome in context of its different extracts, origin and in relationship to its biological effects as analysed using molecular networking and chemometrics. Food Chemistry. 399: 133948. PMID 35994855 DOI: 10.1016/j.foodchem.2022.133948 |
0.456 |
|
| 2022 |
Ware I, Franke K, Hussain H, Morgan I, Rennert R, Wessjohann LA. Bioactive Phenolic Compounds from . Molecules (Basel, Switzerland). 27. PMID 35889234 DOI: 10.3390/molecules27144363 |
0.536 |
|
| 2022 |
Krajnović T, Pantelić NĐ, Wolf K, Eichhorn T, Maksimović-Ivanić D, Mijatović S, Wessjohann LA, Kaluđerović GN. Anticancer Potential of Xanthohumol and Isoxanthohumol Loaded into SBA-15 Mesoporous Silica Particles against B16F10 Melanoma Cells. Materials (Basel, Switzerland). 15. PMID 35888494 DOI: 10.3390/ma15145028 |
0.559 |
|
| 2022 |
Farag MA, Abdelwareth A, Zayed A, Eissa TF, Dokalahy E, Frolov A, Wessjohann LA. A Comparative Metabolomics Approach for Egyptian Mango Fruits Classification Based on UV and UPLC/MS and in Relation to Its Antioxidant Effect. Foods (Basel, Switzerland). 11. PMID 35885370 DOI: 10.3390/foods11142127 |
0.446 |
|
| 2022 |
Farag MA, Zayed A, Sallam IE, Abdelwareth A, Wessjohann LA. Metabolomics-Based Approach for Coffee Beverage Improvement in the Context of Processing, Brewing Methods, and Quality Attributes. Foods (Basel, Switzerland). 11. PMID 35327289 DOI: 10.3390/foods11060864 |
0.444 |
|
| 2022 |
El-Hawary EA, Zayed A, Laub A, Modolo LV, Wessjohann L, Farag MA. How Does LC/MS Compare to UV in Coffee Authentication and Determination of Antioxidant Effects? Brazilian and Middle Eastern Coffee as Case Studies. Antioxidants (Basel, Switzerland). 11. PMID 35052637 DOI: 10.3390/antiox11010131 |
0.446 |
|
| 2022 |
Morgan I, Wessjohann LA, Kaluđerović GN. In Vitro Anticancer Screening and Preliminary Mechanistic Study of A-Ring Substituted Anthraquinone Derivatives. Cells. 11. PMID 35011730 DOI: 10.3390/cells11010168 |
0.608 |
|
| 2022 |
Zayed A, Abdelwareth A, Mohamed TA, Fahmy HA, Porzel A, Wessjohann LA, Farag MA. Dissecting coffee seeds metabolome in context of genotype, roasting degree, and blending in the Middle East using NMR and GC/MS techniques. Food Chemistry. 373: 131452. PMID 34731792 DOI: 10.1016/j.foodchem.2021.131452 |
0.453 |
|
| 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 |
0.552 |
|
| 2021 |
Mamadalieva NZ, Youssef FS, Hussain H, Zengin G, Mollica A, Al Musayeib NM, Ashour ML, Westermann B, Wessjohann LA. Validation of the Antioxidant and Enzyme Inhibitory Potential of Selected Triterpenes Using In Vitro and In Silico Studies, and the Evaluation of Their ADMET Properties. Molecules (Basel, Switzerland). 26. PMID 34770739 DOI: 10.3390/molecules26216331 |
0.511 |
|
| 2021 |
Baky MH, Elshahed MS, Wessjohann LA, Farag MA. Interactions between dietary flavonoids and the gut microbiome: A comprehensive review. The British Journal of Nutrition. 1-46. PMID 34511152 DOI: 10.1017/S0007114521003627 |
0.395 |
|
| 2021 |
Agzamova MA, Mamadalieva NZ, Porzel A, Hussain H, Dube M, Franke K, Janibekov A, Wessjohann LA. Lehmanniaside, a new cycloartane triterpene glycoside from . Natural Product Research. 1-6. PMID 34448421 DOI: 10.1080/14786419.2021.1969563 |
0.512 |
|
| 2021 |
Hegazi NM, Khattab AR, Frolov A, Wessjohann LA, Farag MA. Authentication of saffron spice accessions from its common substitutes via a multiplex approach of UV/VIS fingerprints and UPLC/MS using molecular networking and chemometrics. Food Chemistry. 367: 130739. PMID 34371278 DOI: 10.1016/j.foodchem.2021.130739 |
0.425 |
|
| 2021 |
Shakour ZT, Shehab NG, Gomaa AS, Wessjohann LA, Farag MA. Metabolic and biotransformation effects on dietary glucosinolates, their bioavailability, catabolism and biological effects in different organisms. Biotechnology Advances. 107784. PMID 34102260 DOI: 10.1016/j.biotechadv.2021.107784 |
0.399 |
|
| 2021 |
Pantelić NĐ, Božić B, Zmejkovski BB, Banjac NR, Dojčinović B, Wessjohann LA, Kaluđerović GN. In Vitro Evaluation of Antiproliferative Properties of Novel Organotin(IV) Carboxylate Compounds with Propanoic Acid Derivatives on a Panel of Human Cancer Cell Lines. Molecules (Basel, Switzerland). 26. PMID 34071809 DOI: 10.3390/molecules26113199 |
0.62 |
|
| 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 |
0.546 |
|
| 2021 |
Fayek NM, Mekky RH, Dias CN, Kropf M, Heiss AG, Wessjohann LA, Farag MA. UPLC-MS Metabolome-Based Seed Classification of 16 Vicia Species: A Prospect for Phyto-Equivalency and Chemotaxonomy of Different Accessions. Journal of Agricultural and Food Chemistry. 69: 5252-5266. PMID 33877831 DOI: 10.1021/acs.jafc.0c06054 |
0.433 |
|
| 2021 |
Akramov DK, Mamadalieva NZ, Porzel A, Hussain H, Dube M, Akhmedov A, Altyar AE, Ashour ML, Wessjohann LA. Sugar Containing Compounds and Biological Activities of . Molecules (Basel, Switzerland). 26. PMID 33800987 DOI: 10.3390/molecules26061755 |
0.548 |
|
| 2021 |
Farag MA, Sharaf El-Din MG, Selim MA, Owis AI, Abouzid SF, Porzel A, Wessjohann LA, Otify A. Nuclear Magnetic Resonance Metabolomics Approach for the Analysis of Major Legume Sprouts Coupled to Chemometrics. Molecules (Basel, Switzerland). 26. PMID 33540661 DOI: 10.3390/molecules26030761 |
0.44 |
|
| 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 |
0.567 |
|
| 2021 |
Jänicke P, Lennicke C, Meister A, Seliger B, Wessjohann LA, Kaluđerović GN. Fluorescent spherical mesoporous silica nanoparticles loaded with emodin: Synthesis, cellular uptake and anticancer activity. Materials Science & Engineering. C, Materials For Biological Applications. 119: 111619. PMID 33321661 DOI: 10.1016/j.msec.2020.111619 |
0.57 |
|
| 2021 |
Jänicke P, Lennicke C, Meister A, Seliger B, Wessjohann LA, Kaluđerović GN. Fluorescent spherical mesoporous silica nanoparticles loaded with emodin: Synthesis, cellular uptake and anticancer activity Materials Science and Engineering: C. 119: 111619. DOI: 10.1016/j.msec.2020.111619 |
0.563 |
|
| 2020 |
Farag MA, Shakour ZT, Lübken T, Frolov A, Wessjohann LA, Mahrous E. Unraveling the metabolome composition and its implication for Salvadora persica L. use as dental brush via a multiplex approach of NMR and LC-MS metabolomics. Journal of Pharmaceutical and Biomedical Analysis. 193: 113727. PMID 33197832 DOI: 10.1016/j.jpba.2020.113727 |
0.462 |
|
| 2020 |
Pantelić NĐ, Zmejkovski BB, Božić B, Dojčinović B, Banjac NR, Wessjohann LA, Kaluđerović GN. Synthesis, characterization and in vitro biological evaluation of novel organotin(IV) compounds with derivatives of 2-(5-arylidene-2,4-dioxothiazolidin-3-yl)propanoic acid. Journal of Inorganic Biochemistry. 211: 111207. PMID 32801055 DOI: 10.1016/J.Jinorgbio.2020.111207 |
0.643 |
|
| 2020 |
de Moura PHB, de Sousa AA, Porzel A, Wessjohann LA, Leal ICR, Martins RCC. Characterization of Antibacterial Proanthocyanidins of Dalbergia monetaria, an Amazonian Medicinal Plant, by UHPLC-HRMS/MS. Planta Medica. PMID 32483774 DOI: 10.1055/A-1170-8016 |
0.302 |
|
| 2020 |
Ramadan NS, Wessjohann LA, Mocan A, Vodnar DC, El-Sayed NH, El-Toumy SA, Mohamed DA, Aziz ZA, Ehrlich A, Farag MA. Nutrient and Sensory Metabolites Profiling of L. (Starfruit) in the Context of Its Origin and Ripening Stage by GC/MS and Chemometric Analysis. Molecules (Basel, Switzerland). 25. PMID 32455938 DOI: 10.3390/Molecules25102423 |
0.511 |
|
| 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 |
0.592 |
|
| 2020 |
Nugraha AS, Untari LF, Laub A, Porzel A, Franke K, Wessjohann LA. Anthelmintic and antimicrobial activities of three new depsides and ten known depsides and phenols from Indonesian lichen: Ach. Natural Product Research. 1-10. PMID 32375511 DOI: 10.1080/14786419.2020.1761361 |
0.754 |
|
| 2020 |
Farag MA, Abdelwareth A, Sallam IE, El Shorbagi M, Jehmlich N, Fritz-Wallace K, Serena Schäpe S, Rolle-Kampczyk U, Ehrlich A, Wessjohann LA, von Bergen M. Metabolomics reveals impact of seven functional foods on metabolic pathways in a gut microbiota model. Journal of Advanced Research. 23: 47-59. PMID 32071791 DOI: 10.1016/J.Jare.2020.01.001 |
0.494 |
|
| 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 |
0.591 |
|
| 2020 |
Laub A, Sendatzki AK, Palfner G, Wessjohann LA, Schmidt J, Arnold N. HPTLC-DESI-HRMS-Based Profiling of Anthraquinones in Complex Mixtures-A Proof-of-Concept Study Using Crude Extracts of Chilean Mushrooms. Foods (Basel, Switzerland). 9. PMID 32041163 DOI: 10.3390/Foods9020156 |
0.31 |
|
| 2020 |
Chalo DM, Kakudidi E, Origa-Oryem H, Namukobe J, Franke K, Yenesew A, Wessjohann LA. Chemical constituents of the roots of Ormocarpum sennoides subsp. zanzibaricum Biochemical Systematics and Ecology. 93: 104142. DOI: 10.1016/J.Bse.2020.104142 |
0.303 |
|
| 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 |
0.588 |
|
| 2019 |
Drača D, Mijatović S, Krajnović T, Kaluđerović GN, Wessjohann LA, Maksimović-Ivanić D. Synthetic Tubulysin Derivative, Tubugi-1, Against Invasive Melanoma Cells: The Cell Death Triangle. Anticancer Research. 39: 5403-5415. PMID 31570435 DOI: 10.21873/Anticanres.13734 |
0.605 |
|
| 2019 |
Farag MA, Otify AM, El-Sayed AM, Michel CG, ElShebiney SA, Ehrlich A, Wessjohann LA. Sensory Metabolite Profiling in a Date Pit Based Coffee Substitute and in Response to Roasting as Analyzed via Mass Spectrometry Based Metabolomics. Molecules (Basel, Switzerland). 24. PMID 31533283 DOI: 10.3390/Molecules24183377 |
0.535 |
|
| 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 |
0.555 |
|
| 2019 |
Francioso A, Franke K, Villani C, Mosca L, D'Erme M, Frischbutter S, Brandt W, Sanchez-Lamar A, Wessjohann L. Insights into the Phytochemistry of the Cuban Endemic Medicinal Plant : Fideloside, a Novel Bioactive 8--glycosyl 2,3-Dihydroflavonol. Molecules (Basel, Switzerland). 24. PMID 31390787 DOI: 10.3390/Molecules24152855 |
0.318 |
|
| 2019 |
Budragchaa T, Westermann B, Wessjohann LA. Multicomponent synthesis of α-acylamino and α-acyloxy amide derivatives of desmycosin and their activity against gram-negative bacteria. Bioorganic & Medicinal Chemistry. 27: 3237-3247. PMID 31229422 DOI: 10.1016/J.Bmc.2019.05.046 |
0.372 |
|
| 2019 |
Sakna ST, Mocan A, Sultani HN, El-Fiky NM, Wessjohann LA, Farag MA. Metabolites profiling of Ziziphus leaf taxa via UHPLC/PDA/ESI-MS in relation to their biological activities. Food Chemistry. 293: 233-246. PMID 31151607 DOI: 10.1016/J.Foodchem.2019.04.097 |
0.5 |
|
| 2019 |
Farag MA, El Senousy AS, El-Ahmady SH, Porzel A, Wessjohann LA. Comparative metabolome-based classification of Senna drugs: a prospect for phyto-equivalency of its different commercial products. Metabolomics : Official Journal of the Metabolomic Society. 15: 80. PMID 31087208 DOI: 10.1007/S11306-019-1538-X |
0.473 |
|
| 2019 |
Drača D, Mijatović S, Krajnović T, Pristov JB, Đukić T, Kaluđerović GN, Wessjohann LA, Maksimović-Ivanić D. The synthetic tubulysin derivative, tubugi-1, improves the innate immune response by macrophage polarization in addition to its direct cytotoxic effects in a murine melanoma model. Experimental Cell Research. 380: 159-170. PMID 31042500 DOI: 10.1016/J.Yexcr.2019.04.028 |
0.609 |
|
| 2019 |
Krajnović T, Drača D, Kaluđerović GN, Dunđerović D, Mirkov I, Wessjohann LA, Maksimović-Ivanić D, Mijatović S. The hop-derived prenylflavonoid isoxanthohumol inhibits the formation of lung metastasis in B16-F10 murine melanoma model. Food and Chemical Toxicology : An International Journal Published For the British Industrial Biological Research Association. 129: 257-268. PMID 31034931 DOI: 10.1016/J.Fct.2019.04.046 |
0.598 |
|
| 2019 |
Dos Santos CHC, de Carvalho MG, Franke K, Wessjohann L. Dammarane-type triterpenoids from the stem of Ziziphus glaziovii Warm. (Rhamnaceae). Phytochemistry. 162: 250-259. PMID 30965192 DOI: 10.1016/J.Phytochem.2019.03.010 |
0.32 |
|
| 2019 |
Farag MA, Tawfike AF, Donia MS, Ehrlich A, Wessjohann LA. Influence of Pickling Process on and Metabolome as Determined Mass Spectrometry-Based Metabolomics. Molecules (Basel, Switzerland). 24. PMID 30866428 DOI: 10.3390/Molecules24050928 |
0.506 |
|
| 2019 |
Farag MA, El-Kersh DM, Ehrlich A, Choucry MA, El-Seedi H, Frolov A, Wessjohann LA. Variation in Ceratonia siliqua pod metabolome in context of its different geographical origin, ripening stage and roasting process. Food Chemistry. 283: 675-687. PMID 30722926 DOI: 10.1016/J.Foodchem.2018.12.118 |
0.487 |
|
| 2019 |
Seixas N, Ravanello BB, Morgan I, Kaluđerović GN, Wessjohann LA. Chlorambucil Conjugated Ugi Dendrimers with PAMAM-NH₂ Core and Evaluation of Their Anticancer Activity. Pharmaceutics. 11. PMID 30717083 DOI: 10.3390/Pharmaceutics11020059 |
0.62 |
|
| 2019 |
Kufka R, Rennert R, Kaluđerović GN, Weber L, Richter W, Wessjohann LA. Synthesis of a tubugi-1-toxin conjugate by a modulizable disulfide linker system with a neuropeptide Y analogue showing selectivity for hY1R-overexpressing tumor cells. Beilstein Journal of Organic Chemistry. 15: 96-105. PMID 30680044 DOI: 10.3762/Bjoc.15.11 |
0.628 |
|
| 2019 |
Nganou BK, Mbaveng AT, Fobofou SAT, Fankam AG, Bitchagno GTM, Simo Mpetga JD, Wessjohann LA, Kuete V, Efferth T, Tane P. Furoquinolines and dihydrooxazole alkaloids with cytotoxic activity from the stem bark of Araliopsis soyauxii. Fitoterapia. 133: 193-199. PMID 30654126 DOI: 10.1016/J.Fitote.2019.01.003 |
0.321 |
|
| 2019 |
Pantelic N, Lerbs M, Wolf K, Wessjohann L, Kaludjerovic G. In vitro anticancer evaluation of novel triphenyltin(IV) compounds with some N-acetyl-S-naphthoquinonylcysteine derivatives Journal of the Serbian Chemical Society. 84: 1119-1127. DOI: 10.2298/Jsc190322032P |
0.309 |
|
| 2019 |
Dippe M, Bauer A, Porzel A, Funke E, Müller AO, Schmidt J, Beier M, Wessjohann LA. Coenzyme A‐Conjugated Cinnamic Acids – Enzymatic Synthesis of a CoA‐Ester Library and Application in Biocatalytic Cascades to Vanillin Derivatives Advanced Synthesis & Catalysis. 361: 5346-5350. DOI: 10.1002/Adsc.201900892 |
0.349 |
|
| 2018 |
Hauck N, Seixas N, Centeno SP, Schlüßler R, Cojoc G, Müller P, Guck J, Wöll D, Wessjohann LA, Thiele J. Droplet-Assisted Microfluidic Fabrication and Characterization of Multifunctional Polysaccharide Microgels Formed by Multicomponent Reactions. Polymers. 10. PMID 30960980 DOI: 10.3390/Polym10101055 |
0.336 |
|
| 2018 |
Farag MA, Maamoun AA, Meyer A, Wessjohann LA. Salicylic acid and its derivatives elicit the production of diterpenes and sterols in corals and their algal symbionts: a metabolomics approach to elicitor SAR. Metabolomics : Official Journal of the Metabolomic Society. 14: 127. PMID 30830394 DOI: 10.1007/S11306-018-1416-Y |
0.519 |
|
| 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 |
0.606 |
|
| 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 |
0.604 |
|
| 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 |
0.588 |
|
| 2018 |
Krajnović T, Maksimović-Ivanić D, Mijatović S, Drača D, Wolf K, Edeler D, Wessjohann LA, Kaluđerović GN. Drug Delivery System for Emodin Based on Mesoporous Silica SBA-15. Nanomaterials (Basel, Switzerland). 8. PMID 29757198 DOI: 10.3390/Nano8050322 |
0.614 |
|
| 2018 |
Farag MA, Meyer A, Ali SE, Salem MA, Giavalisco P, Westphal H, Wessjohann LA. A comparative metabolomics approach detects stress-specific responses during coral bleaching in soft corals. Journal of Proteome Research. PMID 29671321 DOI: 10.1021/Acs.Jproteome.7B00929 |
0.469 |
|
| 2018 |
Farag MA, Khattab AR, Ehrlich A, Kropf M, Heiss AG, Wessjohann LA. GC/MS-based Metabolites Profiling of Nutrients and Anti-nutrients in Eight Lens and Lupinus Seeds (Fabaceae). Journal of Agricultural and Food Chemistry. PMID 29561614 DOI: 10.1021/Acs.Jafc.8B00369 |
0.505 |
|
| 2018 |
da Silva ICV, Kaluderovic G, de Oliveira PF, Guimaraes DO, Quaresma CH, Porzel A, Muzitano MF, Wessjohann LA, Leal ICR. Apoptosis caused by triterpenes and phytosterols and antioxidant activity of an enriched flavonoid extract and from Passiflora mucronata. Anti-Cancer Agents in Medicinal Chemistry. PMID 29542423 DOI: 10.2174/1871520618666180315090949 |
0.601 |
|
| 2018 |
Rasheed DM, Porzel A, Frolov A, El Seedi HR, Wessjohann LA, Farag MA. Comparative analysis of Hibiscus sabdariffa (roselle) hot and cold extracts in respect to their potential for α-glucosidase inhibition. Food Chemistry. 250: 236-244. PMID 29412917 DOI: 10.1016/J.Foodchem.2018.01.020 |
0.511 |
|
| 2018 |
Farag MA, Labib RM, Noleto C, Porzel A, Wessjohann LA. NMR approach for the authentication of 10 cinnamon spice accessions analyzed via chemometric tools Lwt. 90: 491-498. DOI: 10.1016/J.Lwt.2017.12.069 |
0.513 |
|
| 2017 |
Janković-Tomanić M, Todorović D, Stanivuković Z, Perić Mataruga V, Wessjohann LA, Kaluđerović GN. Mesoporous silica nanoparticles SBA-15 loaded with emodin upregulate the antioxidative defense of Euproctis chrysorrhoea (L.) larvae. Turkish Journal of Biology = Turk Biyoloji Dergisi. 41: 935-942. PMID 30814858 DOI: 10.3906/Biy-1705-76 |
0.609 |
|
| 2017 |
Farag MA, Westphal H, Eissa TF, Wessjohann LA, Meyer A. Effect of Oxylipins, Terpenoid Precursors and Wounding on Soft Corals' Secondary Metabolism as Analyzed via UPLC/MS and Chemometrics. Molecules (Basel, Switzerland). 22. PMID 29232862 DOI: 10.3390/Molecules22122195 |
0.49 |
|
| 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 |
0.611 |
|
| 2017 |
Farag MA, Fekry MI, Al-Hammady MA, Khalil MN, El-Seedi HR, Meyer A, Porzel A, Westphal H, Wessjohann LA. Cytotoxic Effects of Sarcophyton sp. Soft Corals-Is There a Correlation to Their NMR Fingerprints? Marine Drugs. 15. PMID 28677625 DOI: 10.3390/Md15070211 |
0.481 |
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| 2017 |
Farag MA, Ali SE, Hodaya RH, El-Seedi HR, Sultani HN, Laub A, Eissa TF, Abou-Zaid FOF, Wessjohann LA. Phytochemical Profiles and Antimicrobial Activities of Allium cepa Red cv. and A. sativum Subjected to Different Drying Methods: A Comparative MS-Based Metabolomics. Molecules (Basel, Switzerland). 22. PMID 28481316 DOI: 10.3390/Molecules22050761 |
0.505 |
|
| 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 |
0.758 |
|
| 2017 |
Farag MA, Al-Mahdy DA, Meyer A, Westphal H, Wessjohann LA. Metabolomics reveals biotic and abiotic elicitor effects on the soft coral Sarcophyton ehrenbergi terpenoid content. Scientific Reports. 7: 648. PMID 28381824 DOI: 10.1038/S41598-017-00527-8 |
0.498 |
|
| 2017 |
Kaluđerović GN, Abbas M, Kautz HC, Wadaan MA, Lennicke C, Seliger B, Wessjohann LA. Methionine and seleno-methionine type peptide and peptoid building blocks synthesized by five-component five-center reactions. Chemical Communications (Cambridge, England). PMID 28304024 DOI: 10.1039/C7Cc00399D |
0.649 |
|
| 2017 |
Natalio F, Wiese S, Brandt W, Wessjohann L. Reconstitution of vanadium haloperoxidase's catalytic activity by boric acid - towards a potential biocatalytic role of boron. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28248430 DOI: 10.1002/Chem.201605230 |
0.314 |
|
| 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 |
0.614 |
|
| 2017 |
Farag MA, Ammar NM, Kholeif TE, Metwally NS, El-Sheikh NM, Wessjohann LA, Abdel-Hamid AZ. Rats' urinary metabolomes reveal the potential roles of functional foods and exercise in obesity management. Food & Function. PMID 28197590 DOI: 10.1039/C6Fo01753C |
0.447 |
|
| 2017 |
Bastos KX, Dias CN, Nascimento YM, da Silva MS, Langassner SM, Wessjohann LA, Tavares JF. Identification of Phenolic Compounds from Hancornia speciosa (Apocynaceae) Leaves by UHPLC Orbitrap-HRMS. Molecules (Basel, Switzerland). 22. PMID 28098848 DOI: 10.3390/Molecules22010143 |
0.322 |
|
| 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 |
0.627 |
|
| 2017 |
Otto A, Porzel A, Westermann B, Brandt W, Wessjohann L, Arnold N. Structural and stereochemical elucidation of new hygrophorones from Hygrophorus abieticola (Basidiomycetes) Tetrahedron. 73: 1682-1690. DOI: 10.1016/J.Tet.2017.02.013 |
0.322 |
|
| 2016 |
Moni L, Banfi L, Basso A, Bozzano A, Spallarossa M, Wessjohann L, Riva R. Passerini Reactions on Biocatalytically Derived Chiral Azetidines. Molecules (Basel, Switzerland). 21. PMID 27589709 DOI: 10.3390/Molecules21091153 |
0.382 |
|
| 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 |
0.619 |
|
| 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 |
0.605 |
|
| 2016 |
Shaaban S, Negm A, Ashmawy AM, Ahmed DM, Wessjohann LA. Combinatorial synthesis, in silico, molecular and biochemical studies of tetrazole-derived organic selenides with increased selectivity against hepatocellular carcinoma. European Journal of Medicinal Chemistry. 122: 55-71. PMID 27343853 DOI: 10.1016/J.Ejmech.2016.06.005 |
0.328 |
|
| 2016 |
Otto A, Laub A, Wendt L, Porzel A, Schmidt J, Palfner G, Becerra J, Krüger D, Stadler M, Wessjohann L, Westermann B, Arnold N. Chilenopeptins A and B, Peptaibols from the Chilean Sepedonium aff. chalcipori KSH 883. Journal of Natural Products. PMID 26953507 DOI: 10.1021/Acs.Jnatprod.5B01018 |
0.3 |
|
| 2016 |
Fobofou SA, Franke K, Porzel A, Brandt W, Wessjohann LA. Tricyclic Acylphloroglucinols from Hypericum lanceolatum and Regioselective Synthesis of Selancins A and B. Journal of Natural Products. 79: 743-53. PMID 26950610 DOI: 10.1021/Acs.Jnatprod.5B00673 |
0.344 |
|
| 2016 |
Farag MA, Porzel A, Al-Hammady MA, Hegazy ME, Meyer A, Mohamed TA, Westphal H, Wessjohann LA. Soft Corals Biodiversity in the Egyptian Red Sea: A Comparative MS and NMR Metabolomics Approach of Wild and Aquarium Grown Species. Journal of Proteome Research. 15: 1274-87. PMID 26892921 DOI: 10.1021/Acs.Jproteome.6B00002 |
0.492 |
|
| 2016 |
Farag MA, Otify A, Porzel A, Michel CG, Elsayed A, Wessjohann LA. Comparative metabolite profiling and fingerprinting of genus Passiflora leaves using a multiplex approach of UPLC-MS and NMR analyzed by chemometric tools. Analytical and Bioanalytical Chemistry. 408: 3125-43. PMID 26883968 DOI: 10.1007/S00216-016-9376-4 |
0.504 |
|
| 2016 |
Fobofou SA, Harmon CR, Lonfouo AH, Franke K, Wright SM, Wessjohann LA. Prenylated phenyl polyketides and acylphloroglucinols from Hypericum peplidifolium. Phytochemistry. 124: 108-13. PMID 26880290 DOI: 10.1016/J.Phytochem.2016.02.003 |
0.325 |
|
| 2016 |
Bilova T, Lukasheva E, Brauch D, Greifenhagen U, Paudel G, Tarakhovskaya E, Frolova N, Mittasch J, Balcke GU, Tissier A, Osmolovskaya N, Vogt T, Wessjohann LA, Birkemeyer C, Milkowski C, et al. A Snapshot of the Plant Glycated Proteome: Structural, Functional and Mechanistic Aspects. The Journal of Biological Chemistry. PMID 26786108 DOI: 10.1074/Jbc.M115.678581 |
0.309 |
|
| 2016 |
Krajnović T, Kaluđerović GN, Wessjohann LA, Mijatović S, Maksimović-Ivanić D. Versatile antitumor potential of isoxanthohumol: Enhancement of paclitaxel activity in vivo. Pharmacological Research. 105: 62-73. PMID 26784390 DOI: 10.1016/J.Phrs.2016.01.011 |
0.606 |
|
| 2016 |
Farag MA, Handoussa H, Fekry MI, Wessjohann LA. Metabolite profiling in 18 Saudi date palm fruit cultivars and their antioxidant potential via UPLC-qTOF-MS and multivariate data analyses. Food & Function. 7: 1077-86. PMID 26781334 DOI: 10.1039/C5Fo01570G |
0.515 |
|
| 2016 |
Shaaban S, Negm A, Sobh MA, Wessjohann LA. Expeditious Entry to Functionalized Pseudo-peptidic Organoselenide Redox Modulators via Sequential Ugi/SN Methodology. Anti-Cancer Agents in Medicinal Chemistry. 16: 621-32. PMID 26373394 DOI: 10.2174/1871520615666150916092035 |
0.355 |
|
| 2016 |
El-Sayed MT, Wessjohann L, Porzel A, Hilgeroth A. Diazatruxenes from the Condensation Reaction of Indoles with Ninhydrin Journal of Heterocyclic Chemistry. 54: 1077-1083. DOI: 10.1002/Jhet.2677 |
0.387 |
|
| 2016 |
Wessjohann LA, Wild H, Ferreira LA, Schrekker HS. Synthesis of α-alkenyl-β-hydroxy adducts by α-addition of unprotected 4-bromocrotonic acid and amides with aldehydes and ketones by chromium(II)-mediated reactions Applied Organometallic Chemistry. 30: 674-679. DOI: 10.1002/Aoc.3488 |
0.313 |
|
| 2015 |
Otto A, Porzel A, Schmidt J, Brandt W, Wessjohann L, Arnold N. Structure and Absolute Configuration of Pseudohygrophorones A(12) and B(12), Alkyl Cyclohexenone Derivatives from Hygrophorus abieticola (Basidiomycetes). Journal of Natural Products. PMID 26722697 DOI: 10.1021/Acs.Jnatprod.5B00675 |
0.305 |
|
| 2015 |
Nagel R, Bernholz C, Vranová E, Košuth J, Bergau N, Ludwig S, Wessjohann L, Gershenzon J, Tissier A, Schmidt A. Arabidopsis thaliana isoprenyl diphosphate synthases produce the C25 intermediate, geranylfarnesyl diphosphate. The Plant Journal : For Cell and Molecular Biology. PMID 26505977 DOI: 10.1111/Tpj.13064 |
0.306 |
|
| 2015 |
Farag MA, Sakna ST, El-Fiky NM, Shabana MM, Wessjohann LA. Phytochemical, antioxidant and antidiabetic evaluation of eight Bauhinia L. species from Egypt using UHPLC-PDA-qTOF-MS and chemometrics. Phytochemistry. 119: 41-50. PMID 26410474 DOI: 10.1016/J.Phytochem.2015.09.004 |
0.503 |
|
| 2015 |
Fobofou SA, Franke K, Sanna G, Porzel A, Bullita E, La Colla P, Wessjohann LA. Isolation and anticancer, anthelminthic, and antiviral (HIV) activity of acylphloroglucinols, and regioselective synthesis of empetrifranzinans from Hypericum roeperianum. Bioorganic & Medicinal Chemistry. 23: 6327-34. PMID 26358281 DOI: 10.1016/J.Bmc.2015.08.028 |
0.322 |
|
| 2015 |
Farag MA, Porzel A, Wessjohann LA. Unraveling the active hypoglycemic agent trigonelline in Balanites aegyptiaca date fruit using metabolite fingerprinting by NMR. Journal of Pharmaceutical and Biomedical Analysis. 115: 383-7. PMID 26275727 DOI: 10.1016/J.Jpba.2015.08.003 |
0.497 |
|
| 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 |
0.588 |
|
| 2015 |
Shaaban S, Negm A, Sobh MA, Wessjohann LA. Organoselenocyanates and symmetrical diselenides redox modulators: Design, synthesis and biological evaluation. European Journal of Medicinal Chemistry. 97: 190-201. PMID 25969171 DOI: 10.1016/J.Ejmech.2015.05.002 |
0.329 |
|
| 2015 |
Farag MA, Porzel A, Wessjohann LA. Unequivocal glycyrrhizin isomer determination and comparative in vitro bioactivities of root extracts in four Glycyrrhiza species. Journal of Advanced Research. 6: 99-104. PMID 25685548 DOI: 10.1016/J.Jare.2014.05.001 |
0.477 |
|
| 2015 |
Brauer MC, Neves Filho RA, Westermann B, Heinke R, Wessjohann LA. Synthesis of antibacterial 1,3-diyne-linked peptoids from an Ugi-4CR/Glaser coupling approach. Beilstein Journal of Organic Chemistry. 11: 25-30. PMID 25670988 DOI: 10.3762/Bjoc.11.4 |
0.381 |
|
| 2015 |
Farag MA, Porzel A, Mahrous EA, El-Massry MM, Wessjohann LA. Integrated comparative metabolite profiling via MS and NMR techniques for Senna drug quality control analysis. Analytical and Bioanalytical Chemistry. 407: 1937-49. PMID 25577360 DOI: 10.1007/S00216-014-8432-1 |
0.509 |
|
| 2015 |
Bobach C, Tennstedt S, Palberg K, Denkert A, Brandt W, de Meijere A, Seliger B, Wessjohann LA. Screening of synthetic and natural product databases: Identification of novel androgens and antiandrogens. European Journal of Medicinal Chemistry. 90: 267-79. PMID 25461327 DOI: 10.1016/J.Ejmech.2014.11.026 |
0.526 |
|
| 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 |
0.614 |
|
| 2015 |
Welsch SJ, Umkehrer M, Kalinski C, Ross G, Burdack C, Kolb J, Wild M, Ehrlich A, Wessjohann LA. Synthesis of substituted imidazolines by an Ugi/Staudinger/aza-Wittig sequence Tetrahedron Letters. 56: 1025-1029. DOI: 10.1016/J.Tetlet.2015.01.043 |
0.329 |
|
| 2015 |
Bitchagno GTM, Tankeo SB, Tsopmo A, Mpetga JDS, Tchinda AT, Fobofou SAT, Wessjohann LA, Kuete V, Tane P. Lemairones A and B: Two new antibacterial tetraflavonoids from the leaves of Zanthoxylum lemairei (Rutaceae) Phytochemistry Letters. 14: 1-7. DOI: 10.1016/J.Phytol.2015.08.012 |
0.306 |
|
| 2015 |
Bette E, Otto A, Dräger T, Merzweiler K, Arnold N, Wessjohann L, Westermann B. Isolation and Asymmetric Total Synthesis of Fungal Secondary Metabolite Hygrophorone B12 European Journal of Organic Chemistry. 2015: 2357-2365. DOI: 10.1002/Ejoc.201403455 |
0.338 |
|
| 2014 |
Farag MA, Mohsen M, Heinke R, Wessjohann LA. Metabolomic fingerprints of 21 date palm fruit varieties from Egypt using UPLC/PDA/ESI-qTOF-MS and GC-MS analyzed by chemometrics. Food Research International (Ottawa, Ont.). 64: 218-226. PMID 30011643 DOI: 10.1016/J.Foodres.2014.06.021 |
0.512 |
|
| 2014 |
El Senousy AS, Farag MA, Al-Mahdy DA, Wessjohann LA. Developmental changes in leaf phenolics composition from three artichoke cvs. (Cynara scolymus) as determined via UHPLC-MS and chemometrics. Phytochemistry. 108: 67-76. PMID 25301664 DOI: 10.1016/J.Phytochem.2014.09.004 |
0.499 |
|
| 2014 |
Otto A, Porzel A, Schmidt J, Wessjohann L, Arnold N. Penarines A-F, (nor-)sesquiterpene carboxylic acids from Hygrophorus penarius (Basidiomycetes). Phytochemistry. 108: 229-33. PMID 25269661 DOI: 10.1016/J.Phytochem.2014.09.005 |
0.328 |
|
| 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 |
0.588 |
|
| 2014 |
Barreto Ade F, Vercillo OE, Wessjohann LA, Andrade CK. Consecutive isocyanide-based multicomponent reactions: synthesis of cyclic pentadepsipeptoids. Beilstein Journal of Organic Chemistry. 10: 1017-22. PMID 24991252 DOI: 10.3762/Bjoc.10.101 |
0.794 |
|
| 2014 |
Farag MA, Abdelfattah MS, Badr SE, Wessjohann LA. Profiling the chemical content of Ficus lyrata extracts via UPLC-PDA-qTOF-MS and chemometrics. Natural Product Research. 28: 1549-56. PMID 24934244 DOI: 10.1080/14786419.2014.926353 |
0.512 |
|
| 2014 |
Tanemossu SA, Franke K, Arnold N, Schmidt J, Wabo HK, Tane P, Wessjohann LA. Rare biscoumarin derivatives and flavonoids from Hypericum riparium. Phytochemistry. 105: 171-7. PMID 24930002 DOI: 10.1016/J.Phytochem.2014.05.008 |
0.363 |
|
| 2014 |
Rampon DS, Wessjohann LA, Schneider PH. Palladium-catalyzed direct arylation of selenophene. The Journal of Organic Chemistry. 79: 5987-92. PMID 24893620 DOI: 10.1021/Jo500094T |
0.645 |
|
| 2014 |
Farag MA, Gad HA, Heiss AG, Wessjohann LA. Metabolomics driven analysis of six Nigella species seeds via UPLC-qTOF-MS and GC-MS coupled to chemometrics Food Chemistry. 151: 333-342. PMID 24423541 DOI: 10.1016/J.Foodchem.2013.11.032 |
0.478 |
|
| 2014 |
Wessjohann LA, Dessoy MA. An efficient method for the preparation of silyl esters of diphosphoric, phosphoric, and phosphorous acid Polyhedron. 70: 133-137. DOI: 10.1016/J.Poly.2013.12.024 |
0.346 |
|
| 2013 |
Farag MA, Wessjohann LA. Cytotoxic effect of commercial Humulus lupulus L. (hop) preparations - In comparison to its metabolomic fingerprint. Journal of Advanced Research. 4: 417-21. PMID 25685448 DOI: 10.1016/J.Jare.2012.07.006 |
0.507 |
|
| 2013 |
Farag MA, Weigend M, Luebert F, Brokamp G, Wessjohann LA. Phytochemical, phylogenetic, and anti-inflammatory evaluation of 43 Urtica accessions (stinging nettle) based on UPLC-Q-TOF-MS metabolomic profiles. Phytochemistry. 96: 170-83. PMID 24169378 DOI: 10.1016/J.Phytochem.2013.09.016 |
0.504 |
|
| 2013 |
Wessjohann LA, Scheid GO, Eichelberger U, Umbreen S. Total synthesis of epothilone D: the nerol/macroaldolization approach. The Journal of Organic Chemistry. 78: 10588-95. PMID 24079664 DOI: 10.1021/Jo401355R |
0.312 |
|
| 2013 |
Farag MA, El-Ahmady SH, Elian FS, Wessjohann LA. Metabolomics driven analysis of artichoke leaf and its commercial products via UHPLC-q-TOF-MS and chemometrics. Phytochemistry. 95: 177-87. PMID 23902683 DOI: 10.1016/J.Phytochem.2013.07.003 |
0.522 |
|
| 2013 |
Wessjohann LA, Schneider A, Kaluđerović GN, Brandt W. Solid-phase synthesis of reduced selenocysteine tetrapeptides and their oxidized analogs containing selenenylsulfide eight-membered rings. Molecular Diversity. 17: 537-45. PMID 23729025 DOI: 10.1007/S11030-013-9454-X |
0.656 |
|
| 2013 |
Schmidts V, Fredersdorf M, Lübken T, Porzel A, Arnold N, Wessjohann L, Thiele CM. RDC-based determination of the relative configuration of the fungicidal cyclopentenone 4,6-diacetylhygrophorone A12.. Journal of Natural Products. 76: 839-44. PMID 23659349 DOI: 10.1021/Np300728B |
0.302 |
|
| 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 |
0.598 |
|
| 2013 |
Westermann B, Wessjohann L, Gulyas-Fekete G, Boluda C. Anti-Friedel-Crafts-Type Substitution To Form Biaryl Linkages Synthesis. 45: 3038-3043. DOI: 10.1055/S-0033-1339682 |
0.322 |
|
| 2013 |
Lüdtke D, Wouters A, Bessa A, Sachini M, Wessjohann L. Boron-Zinc Exchange in The Diastereoselective Arylation of Sugar-Based Aldehydes: Stereoselective Synthesis of (+)-7-epi-Goniofufurone and Analogues Synthesis. 45: 2222-2233. DOI: 10.1055/S-0033-1339285 |
0.376 |
|
| 2013 |
Simas NK, Dellamora EdCL, Schripsema J, Lage CLS, Filho AMdO, Wessjohann L, Porzel A, Kuster RM. Acetylenic 2-phenylethylamides and new isobutylamides from Acmella oleracea (L.) R. K. Jansen, a Brazilian spice with larvicidal activity on Aedes aegypti Phytochemistry Letters. 6: 67-72. DOI: 10.1016/J.Phytol.2012.10.016 |
0.333 |
|
| 2013 |
Porzel A, Farag MA, Mülbradt J, Wessjohann LA. Metabolite profiling and fingerprinting of Hypericum species: a comparison of MS and NMR metabolomics Metabolomics. 10: 574-588. DOI: 10.1007/S11306-013-0609-7 |
0.472 |
|
| 2013 |
Farag MA, Mahrous EA, Lübken T, Porzel A, Wessjohann L. Classification of commercial cultivars of Humulus lupulus L. (hop) by chemometric pixel analysis of two dimensional nuclear magnetic resonance spectra Metabolomics. 10: 21-32. DOI: 10.1007/S11306-013-0547-4 |
0.504 |
|
| 2012 |
Neves Filho RA, Stark S, Westermann B, Wessjohann LA. The multicomponent approach to N-methyl peptides: total synthesis of antibacterial (-)-viridic acid and analogues. Beilstein Journal of Organic Chemistry. 8: 2085-90. PMID 23209543 DOI: 10.3762/Bjoc.8.234 |
0.401 |
|
| 2012 |
Farag MA, Wessjohann LA. Volatiles profiling in medicinal licorice roots using steam distillation and solid-phase microextraction (SPME) coupled to chemometrics. Journal of Food Science. 77: C1179-84. PMID 23126623 DOI: 10.1111/J.1750-3841.2012.02927.X |
0.461 |
|
| 2012 |
Abbas M, Wessjohann LA. Direct synthesis of sensitive selenocysteine peptides by the Ugi reaction. Organic & Biomolecular Chemistry. 10: 9330-3. PMID 23114693 DOI: 10.1039/C2Ob26552D |
0.356 |
|
| 2012 |
Béres T, Gemrotová M, Tarkowski P, Ganzera M, Maier V, Friedecký D, Dessoy MA, Wessjohann LA, Spíchal L, Strnad M, Doležal K. Analysis of cytokinin nucleotides by capillary zone electrophoresis with diode array and mass spectrometric detection in a recombinant enzyme in vitro reaction. Analytica Chimica Acta. 751: 176-81. PMID 23084068 DOI: 10.1016/J.Aca.2012.08.049 |
0.317 |
|
| 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 |
0.639 |
|
| 2012 |
Farag MA, Porzel A, Wessjohann LA. Comparative metabolite profiling and fingerprinting of medicinal licorice roots using a multiplex approach of GC-MS, LC-MS and 1D NMR techniques. Phytochemistry. 76: 60-72. PMID 22336263 DOI: 10.1016/J.Phytochem.2011.12.010 |
0.504 |
|
| 2012 |
Farag MA, Wessjohann LA. Metabolome classification of commercial Hypericum perforatum (St. John's Wort) preparations via UPLC-qTOF-MS and chemometrics. Planta Medica. 78: 488-96. PMID 22271082 DOI: 10.1055/S-0031-1298170 |
0.517 |
|
| 2012 |
Gatica-Arias A, Farag MA, Stanke M, Matoušek J, Wessjohann L, Weber G. Flavonoid production in transgenic hop (Humulus lupulus L.) altered by PAP1/MYB75 from Arabidopsis thaliana L. Plant Cell Reports. 31: 111-119. PMID 21912858 DOI: 10.1007/S00299-011-1144-5 |
0.471 |
|
| 2012 |
Neves Filho RA, Stark S, Morejon MC, Westermann B, Wessjohann LA. 4-Isocyanopermethylbutane-1,1,3-triol (IPB): a convertible isonitrile for multicomponent reactions Tetrahedron Letters. 53: 5360-5363. DOI: 10.1016/J.Tetlet.2012.07.064 |
0.378 |
|
| 2012 |
Welsch SJ, Kalinski C, Umkehrer M, Ross G, Kolb J, Burdack C, Wessjohann LA. Palladium and copper catalyzed cyclizations of hydrazine derived Ugi products: facile synthesis of substituted indazolones and hydroxytriazafluorendiones Tetrahedron Letters. 53: 2298-2301. DOI: 10.1016/J.Tetlet.2012.02.095 |
0.347 |
|
| 2012 |
Tarman K, Palm GJ, Porzel A, Merzweiler K, Arnold N, Wessjohann LA, Unterseher M, Lindequist U. Helicascolide C, a new lactone from an Indonesian marine algicolous strain of Daldinia eschscholzii (Xylariaceae, Ascomycota) Phytochemistry Letters. 5: 83-86. DOI: 10.1016/J.Phytol.2011.10.006 |
0.307 |
|
| 2011 |
Neves Filho RA, Westermann B, Wessjohann LA. Synthesis of (-)-julocrotine and a diversity oriented Ugi-approach to analogues and probes. Beilstein Journal of Organic Chemistry. 7: 1504-7. PMID 22238524 DOI: 10.3762/Bjoc.7.175 |
0.389 |
|
| 2011 |
Barreto Ade F, Vercillo OE, Birkett MA, Caulfield JC, Wessjohann LA, Andrade CK. Fast and efficient microwave-assisted synthesis of functionalized peptoids via Ugi reactions. Organic & Biomolecular Chemistry. 9: 5024-7. PMID 21637883 DOI: 10.1039/C1Ob05471F |
0.793 |
|
| 2011 |
Tarman K, Lindequist U, Wende K, Porzel A, Arnold N, Wessjohann LA. Isolation of a new natural product and cytotoxic and antimicrobial activities of extracts from fungi of Indonesian marine habitats. Marine Drugs. 9: 294-306. PMID 21556160 DOI: 10.3390/Md9030294 |
0.771 |
|
| 2011 |
Pando O, Stark S, Denkert A, Porzel A, Preusentanz R, Wessjohann LA. The multiple multicomponent approach to natural product mimics: tubugis, N-substituted anticancer peptides with picomolar activity. Journal of the American Chemical Society. 133: 7692-5. PMID 21528905 DOI: 10.1021/Ja2022027 |
0.41 |
|
| 2011 |
Rodríguez-Díaz M, Delporte C, Cartagena C, Cassels BK, González P, Silva X, León F, Wessjohann LA. Topical anti-inflammatory activity of quillaic acid from Quillaja saponaria Mol. and some derivatives. The Journal of Pharmacy and Pharmacology. 63: 718-24. PMID 21492174 DOI: 10.1111/J.2042-7158.2011.01263.X |
0.309 |
|
| 2011 |
Rashan LJ, Franke K, Khine MM, Kelter G, Fiebig HH, Neumann J, Wessjohann LA. Characterization of the anticancer properties of monoglycosidic cardenolides isolated from Nerium oleander and Streptocaulon tomentosum. Journal of Ethnopharmacology. 134: 781-8. PMID 21291990 DOI: 10.1016/J.Jep.2011.01.038 |
0.763 |
|
| 2011 |
Brandt W, Haupt VJ, Wessjohann LA. Chemoinformatic analysis of biologically active macrocycles. Current Topics in Medicinal Chemistry. 10: 1361-79. PMID 20536415 DOI: 10.2174/156802610792232060 |
0.3 |
|
| 2011 |
Welsch SJ, Umkehrer M, Ross G, Kolb J, Burdack C, Wessjohann LA. PdII/IV catalyzed oxidative cyclization of 1,6-enynes derived by Ugi-4-component reaction Tetrahedron Letters. 52: 6295-6297. DOI: 10.1016/J.Tetlet.2011.09.094 |
0.334 |
|
| 2011 |
Farag MA, Porzel A, Schmidt J, Wessjohann LA. Metabolite profiling and fingerprinting of commercial cultivars of Humulus lupulus L. (hop): a comparison of MS and NMR methods in metabolomics Metabolomics. 8: 492-507. DOI: 10.1007/S11306-011-0335-Y |
0.508 |
|
| 2010 |
Haack M, Löwinger M, Lippmann D, Kipp A, Pagnotta E, Iori R, Monien BH, Glatt H, Brauer MN, Wessjohann LA, Brigelius-Flohé R. Breakdown products of neoglucobrassicin inhibit activation of Nrf2 target genes mediated by myrosinase-derived glucoraphanin hydrolysis products. Biological Chemistry. 391: 1281-93. PMID 20868228 DOI: 10.1515/Bc.2010.134 |
0.302 |
|
| 2010 |
Quang DN, Schmidt J, Porzel A, Wessjohann L, Haid M, Arnold N. Ampullosine, a new isoquinoline alkaloid from Sepedonium ampullosporum (Ascomycetes). Natural Product Communications. 5: 869-72. PMID 20614812 |
0.616 |
|
| 2010 |
Brandt W, Kufka J, Schulze D, Schulze E, Rausch F, Wessjohann L. The membrane bound aromatic p-hydroxybenzoic acid oligoprenyltransferase (UbiA) - how iterative improvements lead to a realistic structure that offers new insights into functional aspects of prenyl transferases and terpene synthases Journal of Cheminformatics. 2. DOI: 10.1186/1758-2946-2-S1-O20 |
0.328 |
|
| 2010 |
Quang DN, Schmidt J, Porzel A, Wessjohann L, Haid M, Arnold N. Ampullosine, a new Isoquinoline Alkaloid from Sepedonium ampullosporum (Ascomycetes) Natural Product Communications. 5: 1934578X1000500. DOI: 10.1177/1934578X1000500609 |
0.648 |
|
| 2010 |
Braga AL, Wessjohann LA, Taube PS, Galetto FZ, De Andrade FM. Straightforward method for the synthesis of selenocysteine and selenocystine derivatives from L-serine methyl ester Synthesis. 3131-3137. DOI: 10.1055/S-0030-1258188 |
0.626 |
|
| 2010 |
Westermann B, Henze M, Kreye O, Brauch S, Nitsche C, Naumann K, Wessjohann L. Photoaffinity-Labeled Peptoids and Depsipeptides by Multicomponent Reactions Synthesis. 2010: 2997-3003. DOI: 10.1055/S-0030-1258182 |
0.353 |
|
| 2010 |
Braga AL, Appelt HR, Schneider PH, Rodrigues OED, Silveira CC, Wessjohann LA. ChemInform Abstract: New C2-Symmetric Chiral Disulfide Ligands Derived from (R)-Cysteine. Cheminform. 32: no-no. DOI: 10.1002/chin.200130036 |
0.572 |
|
| 2010 |
Braga AL, Appelt HR, Schneider PH, Silveira CC, Wessjohann LA. ChemInform Abstract: A New Functionalized, Chiral Disulfide Derived from L-Cysteine: (R,R)-Bis[(3-benzyloxazolan-4-yl)methane] Disulfide as a Catalyst in the Diethylzinc Addition to Aldehydes. Cheminform. 30: no-no. DOI: 10.1002/chin.199942037 |
0.575 |
|
| 2010 |
Braga AL, Dornelles L, Silveira CC, Wessjohann LA. ChemInform Abstract: Lewis Acid Mediated Selective Chalcogenalkylation of Silyl Enol Ethers with [O,S]-Acetals. Cheminform. 30: no-no. DOI: 10.1002/chin.199932064 |
0.623 |
|
| 2010 |
WENDER PA, WESSJOHANN LA, PESCHKE B, RAWLINS DB. ChemInform Abstract: The Pinene Path to Taxol: Readily Accessible A-Ring Building Blocks Based on Novel Alkyl- and Alkenyllithium Reagents with Internal Carbonyl Groups. Cheminform. 27: no-no. DOI: 10.1002/chin.199603197 |
0.433 |
|
| 2010 |
BRAGA AL, SILVEIRA CC, DORNELLES L, ZENI G, GALARZA FAD, WESSJOHANN LA. ChemInform Abstract: Catalyst-Dependent Selective Synthesis of O/S- and S/S-Acetals from Enol Ethers. Cheminform. 26: no-no. DOI: 10.1002/chin.199551079 |
0.618 |
|
| 2009 |
Pando O, Dörner S, Preusentanz R, Denkert A, Porzel A, Richter W, Wessjohann L. First total synthesis of tubulysin B. Organic Letters. 11: 5567-9. PMID 19919080 DOI: 10.1021/Ol902320W |
0.324 |
|
| 2009 |
Brandt W, Bräuer L, Günnewich N, Kufka J, Rausch F, Schulze D, Schulze E, Weber R, Zakharova S, Wessjohann L. Molecular and structural basis of metabolic diversity mediated by prenyldiphosphate converting enzymes. Phytochemistry. 70: 1758-75. PMID 19878958 DOI: 10.1016/J.Phytochem.2009.09.001 |
0.654 |
|
| 2009 |
Mecklenburg S, Shaaban S, Ba LA, Burkholz T, Schneider T, Diesel B, Kiemer AK, Röseler A, Becker K, Reichrath J, Stark A, Tilgen W, Abbas M, Wessjohann LA, Sasse F, et al. Exploring synthetic avenues for the effective synthesis of selenium- and tellurium-containing multifunctional redox agents. Organic & Biomolecular Chemistry. 7: 4753-62. PMID 19865713 DOI: 10.1039/B907831B |
0.353 |
|
| 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 |
0.64 |
|
| 2009 |
Shabaan S, Ba LA, Abbas M, Burkholz T, Denkert A, Gohr A, Wessjohann LA, Sasse F, Weber W, Jacob C. Multicomponent reactions for the synthesis of multifunctional agents with activity against cancer cells. Chemical Communications (Cambridge, England). 4702-4. PMID 19641815 DOI: 10.1039/B823149D |
0.794 |
|
| 2009 |
Leal IC, dos Santos KR, Júnior II, Antunes OA, Porzel A, Wessjohann L, Kuster RM. Ceanothane and lupane type triterpenes from Zizyphus joazeiro - an anti-staphylococcal evaluation. Planta Medica. 76: 47-52. PMID 19639538 DOI: 10.1055/S-0029-1185947 |
0.308 |
|
| 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 |
0.614 |
|
| 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 |
0.785 |
|
| 2009 |
Wessjohann L, Zakharova S, Schulze D, Kufka J, Weber R, Brauer L, Brandt W. Enzymatic C-C-coupling prenylation: Bioinformatics-modelling-mechanism- protein-redesign-biocatalytic application Chimia. 63: 340-344. DOI: 10.2533/Chimia.2009.340 |
0.646 |
|
| 2008 |
Quang DN, Spiteller P, Porzel A, Schmidt J, Geissler T, Arnold N, Wessjohann L. Alkaloids from the mushroom Pseudobaeospora pyrifera, pyriferines A-C. Journal of Natural Products. 71: 1620-2. PMID 18771319 DOI: 10.1021/Np800365F |
0.651 |
|
| 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 |
0.624 |
|
| 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 |
0.79 |
|
| 2008 |
Teichert A, Schmidt J, Porzel A, Arnold N, Wessjohann L. (Iso)-quinoline alkaloids from fungal fruiting bodies of Cortinarius subtortus Journal of Natural Products. 71: 1092-1094. PMID 18447384 DOI: 10.1021/Np8000859 |
0.316 |
|
| 2008 |
Wessjohann LA, Schneider A. Synthesis of selenocysteine and its derivatives with an emphasis on selenenylsulfide (-Se-S-) formation. Chemistry & Biodiversity. 5: 375-88. PMID 18357547 DOI: 10.1002/Cbdv.200890038 |
0.385 |
|
| 2008 |
Bräuer L, Brandt W, Schulze D, Zakharova S, Wessjohann L. A structural model of the membrane-bound aromatic prenyltransferase UbiA from E. coli. Chembiochem : a European Journal of Chemical Biology. 9: 982-92. PMID 18338424 DOI: 10.1002/Cbic.200700575 |
0.638 |
|
| 2008 |
Dumri K, Seipold L, Schmidt J, Gerlach G, Dötterl S, Ellis AG, Wessjohann LA. Non-volatile floral oils of Diascia spp. (Scrophulariaceae). Phytochemistry. 69: 1372-83. PMID 18329058 DOI: 10.1016/J.Phytochem.2007.12.012 |
0.759 |
|
| 2008 |
Braga AL, Paixão MW, Westermann B, Schneider PH, Wessjohann LA. Acceleration of arylzinc formation and its enantioselective addition to aldehydes by microwave irradiation and aziridine-2-methanol catalysts. The Journal of Organic Chemistry. 73: 2879-82. PMID 18315002 DOI: 10.1021/Jo702413N |
0.795 |
|
| 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 |
0.61 |
|
| 2008 |
Vercillo OE, Andrade CK, Wessjohann LA. Design and synthesis of cyclic RGD pentapeptoids by consecutive Ugi reactions. Organic Letters. 10: 205-8. PMID 18088132 DOI: 10.1021/Ol702521G |
0.796 |
|
| 2008 |
Rhoden CRB, Westermann B, Wessjohann LA. One-pot multicomponent synthesis of N-substituted tryptophan-derived diketopiperazines Synthesis. 2077-2082. DOI: 10.1055/S-2008-1067112 |
0.366 |
|
| 2008 |
Wessjohann LA, Schmidt G, Schrekker HS. Reaction of secondary and tertiary aliphatic halides with aromatic aldehydes mediated by chromium(II): a selective cross-coupling of alkyl and ketyl radicals Tetrahedron. 64: 2134-2142. DOI: 10.1016/J.Tet.2007.12.039 |
0.344 |
|
| 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 |
0.507 |
|
| 2008 |
Braga AL, Paixao MW, Westermann B, Schneider PH, Wessjohann LA. ChemInform Abstract: Acceleration of Arylzinc Formation and Its Enantioselective Addition to Aldehydes by Microwave Irradiation and Aziridine-2-methanol Catalysts. Cheminform. 39. DOI: 10.1002/CHIN.200833102 |
0.573 |
|
| 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 |
0.622 |
|
| 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 |
0.598 |
|
| 2007 |
Anderle C, Hennig S, Kammerer B, Li SM, Wessjohann L, Gust B, Heide L. Improved mutasynthetic approaches for the production of modified aminocoumarin antibiotics. Chemistry & Biology. 14: 955-67. PMID 17719494 DOI: 10.1016/J.Chembiol.2007.07.014 |
0.338 |
|
| 2007 |
Giacomelli SR, Maldaner G, Stücker C, Marasciulo C, Schmidt J, Wessjohann L, Dalcol II, Morel AF. Triterpenoids from Gouania ulmifolia. Planta Medica. 73: 499-501. PMID 17566152 DOI: 10.1055/S-2007-967166 |
0.322 |
|
| 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 |
0.616 |
|
| 2007 |
Wessjohann L, Kreye O, Westermann B. A Stable, Convertible Isonitrile as a Formic Acid Carbanion [-COOH] Equivalent and Its Application in Multicomponent Reactions Synlett. 2007: e3-e3. DOI: 10.1055/S-2007-990912 |
0.381 |
|
| 2007 |
Braga AL, Paixao MW, Westermann B, Schneider PH, Wessjohann LA. Aziridine-modified amino alcohols as efficient modular catalysts for highly enantioselective alkenylzinc additions to aldehydes Synlett. 917-920. DOI: 10.1055/S-2007-973879 |
0.791 |
|
| 2007 |
Braga AL, Paixao MW, Westermann B, Schneider PH, Wessjohann LA. Highly Enantioselective Alkenylzinc Additions to Aldehydes Synfacts. 2007: 603-603. DOI: 10.1055/S-2007-968553 |
0.367 |
|
| 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 |
0.613 |
|
| 2007 |
Wessjohann LA, Schrekker HS. Takai–Utimoto reactions of oxoalkylhalides catalytic in chromium and cobalt Tetrahedron Letters. 48: 4323-4325. DOI: 10.1016/J.Tetlet.2007.04.119 |
0.311 |
|
| 2007 |
Paixao MW, de Godoi M, Rhoden CRB, Westermann B, Wessjohann LA, Lüdtke DS, Braga AL. The application of chiral, non-racemic N-alkylephedrine and N,N-dialkylnorephedrine as ligands for the enantioselective aryl transfer reaction to aldehydes Journal of Molecular Catalysis a: Chemical. 261: 120-124. DOI: 10.1016/J.Molcata.2006.07.076 |
0.741 |
|
| 2007 |
Michalik D, Schaks A, Wessjohann LA. One-Step Synthesis of Natural Product-Inspired Biaryl Ether-Cyclopeptoid Macrocycles by Double Ugi Multiple-Component Reactions of Bifunctional Building Blocks European Journal of Organic Chemistry. 2007: 149-157. DOI: 10.1002/Ejoc.200600354 |
0.378 |
|
| 2007 |
Braga AL, Paixao MW, Westermann B, Schneider PH, Wessjohann LA. Aziridine-Modified Amino Alcohols as Efficient Modular Catalysts for Highly Enantioselective Alkenylzinc Additions to Aldehydes. Cheminform. 38. DOI: 10.1002/CHIN.200732025 |
0.577 |
|
| 2007 |
Zanatta N, Schneider JMFM, Schneider PH, Wouters AD, Bonacorso HG, Martins MAP, Wessjohann LA. Regiospecific Synthesis of 4-Alkoxy and 4-Amino Substituted 2-Trifluoromethyl Pyrroles. Cheminform. 38. DOI: 10.1002/CHIN.200701113 |
0.611 |
|
| 2006 |
Zanatta N, Schneider JM, Schneider PH, Wouters AD, Bonacorso HG, Martins MA, Wessjohann LA. Regiospecific synthesis of 4-alkoxy and 4-amino substituted 2-trifluoromethyl pyrroles. The Journal of Organic Chemistry. 71: 6996-8. PMID 16930054 DOI: 10.1021/Jo061058K |
0.658 |
|
| 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 |
0.602 |
|
| 2006 |
Abbas M, Bethke J, Wessjohann LA. One pot synthesis of selenocysteine containing peptoid libraries by Ugi multicomponent reactions in water. Chemical Communications (Cambridge, England). 541-3. PMID 16432576 DOI: 10.1039/B514597J |
0.343 |
|
| 2006 |
Odman P, Wessjohann LA, Bornscheuer UT. Chemoenzymatic dynamic kinetic resolution of acyloins. The Journal of Organic Chemistry. 70: 9551-5. PMID 16268632 DOI: 10.1021/Jo051661N |
0.367 |
|
| 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 |
0.604 |
|
| 2006 |
Zanatta N, Schneider J, Schneider P, Wouters A, Bonacorso H, Martins M, Wessjohann L. Synthesis of Trifluoromethyl Pyrroles Synfacts. 2006: 1216-1216. DOI: 10.1055/S-2006-955564 |
0.631 |
|
| 2006 |
De Greef M, Abeln S, Belkasmi K, Dömling A, Orru RVA, Wessjohann LA. Rapid combinatorial access to macrocyclic ansapeptoids and ansapeptides with natural-product-like core structures Synthesis. 3997-4004. DOI: 10.1055/S-2006-950335 |
0.402 |
|
| 2006 |
Schneider A, Rodrigues OED, Paixão MW, Appelt HR, Braga AL, Wessjohann LA. Stereoselective synthesis of Boc-protected L-seleno- and tellurolanthionine, L-seleno- and tellurocystine and derivatives Tetrahedron Letters. 47: 1019-1021. DOI: 10.1016/J.Tetlet.2005.11.101 |
0.702 |
|
| 2006 |
Wilhelm H, Wessjohann LA. An efficient synthesis of the phytoestrogen 8-prenylnaringenin from xanthohumol by a novel demethylation process Tetrahedron. 62: 6961-6966. DOI: 10.1016/J.Tet.2006.04.060 |
0.325 |
|
| 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 |
0.574 |
|
| 2006 |
Braga AL, Vargas F, Sehnem JA, Wessjohann LA. Microwave-mediated palladium-catalyzed asymmetric allylic alkylation using chiral β-seleno amides European Journal of Organic Chemistry. 4993-4997. DOI: 10.1002/Ejoc.200600707 |
0.626 |
|
| 2006 |
Braga AL, Luedtke DS, Schneider PH, Vargas F, Schneider A, Wessjohann LA, Paixao MW. Catalytic Enantioselective Aryl Transfer: Asymmetric Addition of Boronic Acids to Aldehydes Using Pyrrolidinylmethanols as Ligands. Cheminform. 37. DOI: 10.1002/CHIN.200607099 |
0.598 |
|
| 2005 |
Wessjohann LA, Ruijter E, Garcia-Rivera D, Brandt W. What can a chemist learn from nature's macrocycles?--a brief, conceptual view. Molecular Diversity. 9: 171-86. PMID 15789564 DOI: 10.1007/S11030-005-1314-X |
0.624 |
|
| 2005 |
Wessjohann LA, Ruijter E. Macrocycles rapidly produced by multiple multicomponent reactions including bifunctional building blocks (MiBs). Molecular Diversity. 9: 159-69. PMID 15789563 DOI: 10.1007/S11030-005-1313-Y |
0.662 |
|
| 2005 |
Ruijter E, Schültingkemper H, Wessjohann LA. Highly substituted tetrahydropyrones from hetero-Diels-Alder reactions of 2-alkenals with stereochemical induction from chiral dienes. The Journal of Organic Chemistry. 70: 2820-3. PMID 15787578 DOI: 10.1021/Jo0488311 |
0.647 |
|
| 2005 |
Zhu M, Ruijter E, Wessjohann LA. New scavenger resin for the reversible linking and monoprotection of functionalized aromatic aldehydes. Organic Letters. 6: 3921-4. PMID 15496064 DOI: 10.1021/Ol048610H |
0.62 |
|
| 2005 |
Braga AL, Alves EF, Silveira CC, Zeni G, Appelt HR, Wessjohann LA. A new cysteine-derived ligand as catalyst for the addition of diethylzinc to aldehydes: The importance of a 'free' sulfide site for enantioselectivity Synthesis. 588-594. DOI: 10.1055/S-2005-861801 |
0.629 |
|
| 2005 |
Braga AL, Lüdtke DS, Schneider PH, Vargas F, Schneider A, Wessjohann LA, Paixão MW. Catalytic enantioselective aryl transfer: Asymmetric addition of boronic acids to aldehydes using pyrrolidinylmethanols as ligands Tetrahedron Letters. 46: 7827-7830. DOI: 10.1016/J.Tetlet.2005.09.026 |
0.806 |
|
| 2005 |
Braga AL, Silveira CC, De Bolster MWG, Schrekker HS, Wessjohann LA, Schneider PH. Microwave-accelerated asymmetric allylations using cysteine derived oxazolidine and thiazolidine palladium complexes Journal of Molecular Catalysis a: Chemical. 239: 235-238. DOI: 10.1016/J.Molcata.2005.06.008 |
0.742 |
|
| 2005 |
Braga AL, Lüdtke DS, Wessjohann LA, Paixão MW, Schneider PH. A chiral disulfide derived from (R)-cysteine in the enantioselective addition of diethylzinc to aldehydes: loading effect and asymmetric amplification Journal of Molecular Catalysis a: Chemical. 229: 47-50. DOI: 10.1016/J.Molcata.2004.11.004 |
0.782 |
|
| 2005 |
Wessjohann LA, Ruijter E. Strategies for Total and Diversity-Oriented Synthesis of Natural Product(-like) Macrocycles Cheminform. 36. DOI: 10.1007/B96883 |
0.653 |
|
| 2004 |
Bräuer L, Brandt W, Wessjohann LA. Modeling the E. coli 4-hydroxybenzoic acid oligoprenyltransferase ( ubiA transferase) and characterization of potential active sites. Journal of Molecular Modeling. 10: 317-27. PMID 15597200 DOI: 10.1007/S00894-004-0197-6 |
0.639 |
|
| 2004 |
Galm U, Dessoy MA, Schmidt J, Wessjohann LA, Heide L. In vitro and in vivo production of new aminocoumarins by a combined biochemical, genetic, and synthetic approach. Chemistry & Biology. 11: 173-83. PMID 15123279 DOI: 10.1016/J.Chembiol.2004.01.012 |
0.347 |
|
| 2004 |
Brandt W, Dessoy MA, Fulhorst M, Gao W, Zenk MH, Wessjohann LA. A proposed mechanism for the reductive ring opening of the cyclodiphosphate MEcPP, a crucial transformation in the new DXP/MEP pathway to isoprenoids based on modeling studies and feeding experiments Chembiochem. 5: 311-323. PMID 14997523 DOI: 10.1002/Cbic.200300743 |
0.311 |
|
| 2004 |
Zakharova S, Fulhorst M, Luczak L, Wessjohann L. Synthesis, inhibitory and activation properties of prenyldiphosphate mimics for aromatic prenylations with ubiA-prenyl transferase Arkivoc. 2004: 79-96. DOI: 10.3998/Ark.5550190.0005.D10 |
0.351 |
|
| 2004 |
Wessjohann LA, Wild H, Schrekker HS. Chromium-mediated aldol and homoaldol reactions on solid support directed towards an iterative polyol strategy Tetrahedron Letters. 45: 9073-9078. DOI: 10.1016/J.Tetlet.2004.10.038 |
0.312 |
|
| 2004 |
Scheid G, Ruijter E, Konarzycka-Bessler M, Bornscheuer UT, Wessjohann LA. Synthesis and resolution of a key building block for epothilones: a comparison of asymmetric synthesis, chemical and enzymatic resolution Tetrahedron: Asymmetry. 15: 2861-2869. DOI: 10.1016/J.Tetasy.2004.06.048 |
0.625 |
|
| 2004 |
Micskei K, Hajdu C, Wessjohann LA, Mercs L, Kiss-Szikszai A, Patonay T. Enantioselective reduction of prochiral ketones by chromium(II) amino acid complexes Tetrahedron: Asymmetry. 15: 1735-1744. DOI: 10.1016/J.Tetasy.2004.04.017 |
0.303 |
|
| 2004 |
Schneider P, Schrekker H, Silveira C, Wessjohann L, Braga A. First Generation Cysteine- and Methionine-Derived Oxazolidine and Thiazolidine Ligands for Palladium-Catalyzed Asymmetric Allylations European Journal of Organic Chemistry. 2004: 2715-2722. DOI: 10.1002/Ejoc.200300675 |
0.757 |
|
| 2004 |
Scheid G, Kuit W, Ruijter E, Orru RVA, Henke E, Bornscheuer U, Wessjohann LA. A new route to protected acyloins and their enzymatic resolution with lipases European Journal of Organic Chemistry. 1063-1074. DOI: 10.1002/Ejoc.200300338 |
0.619 |
|
| 2004 |
Schneider PH, Schrekker HS, Silveira CC, Wessjohann LA, Braga AL. First Generation Cysteine- and Methionine-Derived Oxazolidine and Thiazolidine Ligands for Palladium-Catalyzed Asymmetric Allylations. Cheminform. 35. DOI: 10.1002/chin.200441037 |
0.59 |
|
| 2004 |
Schrekker H, Micskei K, Hajdu C, Patonay T, de Bolster M, Wessjohann L. Involvement of an Oxidation-Reduction Equilibrium in Chromium-Mediated Enantioselective Nozaki–Hiyama Reactions Advanced Synthesis & Catalysis. 346: 731-736. DOI: 10.1002/Adsc.200404021 |
0.324 |
|
| 2003 |
Hoang Anh NT, Van Sung T, Porzel A, Franke K, Wessjohann LA. Homoisoflavonoids from Ophiopogon japonicus Ker-Gawler. Phytochemistry. 62: 1153-8. PMID 12591271 DOI: 10.1016/S0031-9422(02)00515-0 |
0.318 |
|
| 2003 |
Bethke J, Karaghiosoff K, Wessjohann LA. Synthesis of N,N-disubstituted selenoamides by O/Se-exchange with selenium–Lawesson's reagent Tetrahedron Letters. 44: 6911-6913. DOI: 10.1016/S0040-4039(03)01690-3 |
0.307 |
|
| 2003 |
Braga AL, Rubim RM, Schrekker HS, Wessjohann LA, de Bolster MW, Zeni G, Sehnem JA. The facile synthesis of chiral oxazoline catalysts for the diethylzinc addition to aldehydes Tetrahedron: Asymmetry. 14: 3291-3295. DOI: 10.1016/J.Tetasy.2003.08.029 |
0.635 |
|
| 2003 |
Braga AL, Appelt HR, Silveira CC, Wessjohann LA, Schneider PH. Facile and Practical Enantioselective Synthesis of Propargylic Alcohols by Direct Addition of Alkynes to Aldehydes Catalyzed by Chiral Disulfide—Oxazolidine Ligands. Cheminform. 34. DOI: 10.1002/chin.200319054 |
0.593 |
|
| 2003 |
Wessjohann LA, Scheid G. Chapter 35. Synthetic Access to Epothilones-Natural Products with Extraordinary Anticancer Activity Organic Synthesis Set. 251-267. DOI: 10.1002/9783527620784.Ch35C |
0.301 |
|
| 2002 |
Schrekker HS, de Bolster MW, Orru RV, Wessjohann LA. In situ formation of allyl ketones via Hiyama-Nozaki reactions followed by a chromium-mediated Oppenauer oxidation. The Journal of Organic Chemistry. 67: 1975-81. PMID 11925200 DOI: 10.1021/Jo001750U |
0.787 |
|
| 2002 |
Braga AL, Silva SJ, Lüdtke DS, Drekener RL, Silveira CC, Rocha JB, Wessjohann LA. Chiral diselenide ligands for the asymmetric copper-catalyzed conjugate addition of Grignard reagents to enones Tetrahedron Letters. 43: 7329-7331. DOI: 10.1016/S0040-4039(02)01713-6 |
0.617 |
|
| 2002 |
Braga AL, Appelt HR, Silveira CC, Wessjohann LA, Schneider PH. Facile and practical enantioselective synthesis of propargylic alcohols by direct addition of alkynes to aldehydes catalyzed by chiral disulfide–oxazolidine ligands Tetrahedron. 58: 10413-10416. DOI: 10.1016/S0040-4020(02)01420-5 |
0.742 |
|
| 2001 |
Braga AL, Appelt HR, Schneider PH, Rodrigues OE, Silveira CC, Wessjohann LA. New C 2 -symmetric chiral disulfide ligands derived from ( R )-cysteine Tetrahedron. 57: 3291-3295. DOI: 10.1016/S0040-4020(01)00199-5 |
0.738 |
|
| 2000 |
Wessjohann LA. Synthesis of natural-product-based compound libraries. Current Opinion in Chemical Biology. 4: 303-9. PMID 10826981 DOI: 10.1016/S1367-5931(00)00093-4 |
0.325 |
|
| 2000 |
Schulz Lang E, Burrow RA, Braga AL, Appelt HR, Schneider PH, Silveira CC, Wessjohann LA. R,R-(+)-Bis[(3-benzyloxazolan-4-yl)methyl] disulfide Acta Crystallographica Section E Structure Reports Online. 57: o41-o42. DOI: 10.1107/S160053680001878X |
0.716 |
|
| 1999 |
Braga AL, Dornelles L, Silveira CC, Wessjohann LA. Lewis Acid Mediated Selective Chalcogenalkylation of Silyl Enol Ethers with [O,S]-Acetals Synthesis. 1999: 562-564. DOI: 10.1055/S-1999-3429 |
0.742 |
|
| 1999 |
Braga AL, Appelt HR, Schneider PH, Silveira CC, Wessjohann LA. A new functionalized, chiral disulfide derived from l-cysteine: (R,R)-bis[(3-benzyloxazolan-4-yl)-methane] disulfide as a catalyst in the diethylzinc addition to aldehydes Tetrahedron: Asymmetry. 10: 1733-1738. DOI: 10.1016/S0957-4166(99)00145-7 |
0.744 |
|
| 1998 |
Morel AF, Machado EC, Moreira JJ, Menezes AS, Mostardeiro MA, Zanatta N, Wessjohann LA. Cyclopeptide alkaloids of Scutia buxifolia Phytochemistry. 47: 125-129. DOI: 10.1016/S0031-9422(97)00491-3 |
0.346 |
|
| 1998 |
Wessjohann LA, Sinks U. Benzeneselenenyl Reagents in Organic Synthesis Journal F�R Praktische Chemie/Chemiker-Zeitung. 340: 189-203. DOI: 10.1002/Prac.19983400302 |
0.347 |
|
| 1997 |
Wessjohann L, Gabriel T. Chromium(II)-Mediated Reformatsky Reactions of Carboxylic Esters with Aldehydes The Journal of Organic Chemistry. 62: 3772-3774. DOI: 10.1021/Jo961910V |
0.306 |
|
| 1997 |
Gabriel T, Wessjohann L. The chromium-Reformatsky reaction: anti-selective Evans-type aldol reactions with excellent inverse induction at ambient temperature Tetrahedron Letters. 38: 4387-4388. DOI: 10.1016/S0040-4039(97)00952-0 |
0.333 |
|
| 1997 |
Gabriel T, Wessjohann L. The chromium—Reformatsky reaction: Asymmetric synthesis of the aldol fragment of the cytotoxic epothilons from 3-(2-bromoacyl)-2-oxazolidinones Tetrahedron Letters. 38: 1363-1366. DOI: 10.1016/S0040-4039(96)02494-X |
0.374 |
|
| 1997 |
Mostardeiro MA, Ethur EM, Morel AF, Wessjohann LA. Synthesis of Tripeptide Fragments of 14-Membered Cyclopeptide Alkaloids Journal FüR Praktische Chemie/Chemiker-Zeitung. 339: 467-472. DOI: 10.1002/Prac.19973390183 |
0.332 |
|
| 1996 |
Wessjohann L, Sontag B. Prenylation of Benzoic Acid Derivatives Catalyzed by a Transferase fromEscherichia coli Overproduction: Method Development and Substrate Specificity Angewandte Chemie International Edition in English. 35: 1697-1699. DOI: 10.1002/Anie.199616971 |
0.317 |
|
| 1995 |
Braga AL, Silveira CC, Dornelles L, Zeni G, Galarza FAD, Wessjohann LA. Catalyst-Dependent Selective Synthesis of O/S- and S/S-Acetals from Enol Ethers Synthetic Communications. 25: 3155-3162. DOI: 10.1080/00397919508015466 |
0.665 |
|
| 1995 |
Wender PA, Wessjohann LA, Peschke B, Rawlins DB. The pinene path to taxol: Readily accessible a-ring building blocks based on novel alkyl- and alkenyllithium reagents with internal carbonyl groups Tetrahedron Letters. 36: 7181-7184. DOI: 10.1016/0040-4039(95)01491-Y |
0.516 |
|
| 1994 |
Wessjohann L. The First Total Syntheses of Taxol Angewandte Chemie International Edition in English. 33: 959-961. DOI: 10.1002/Anie.199409591 |
0.311 |
|
| 1993 |
Wessjohann L, Giller K, Zuck B, Skatteboel L, de Meijere A. Cyclopropyl building blocks for organic synthesis. Part 22. Facile synthesis of stable analogs of 2-oxocyclobutanecarboxylates: 2-[(diphenylmethylene)amino]cyclobutenecarboxylates, derivatives and reactions The Journal of Organic Chemistry. 58: 6442-6450. DOI: 10.1021/Jo00075A047 |
0.348 |
|
| 1992 |
Wessjohann L, Krass N, Yu D, Meijere AD. A New Versatile Synthesis of Ring‐Substituted 2‐Cyclopropylglycines and Related Amino Acids Chemische Berichte. 125: 867-882. DOI: 10.1002/Cber.19921250418 |
0.386 |
|
| 1989 |
Wessjohann L, Mcgaffin G, de Meijere A. 1,4-Addition of (Diphenylmethylene)amine to Acceptor Substituted Olefins. A Versatile Synthesis of Protected β-Amino Acids, Nitriles, and Ketones Synthesis. 1989: 359-363. DOI: 10.1055/S-1989-27252 |
0.348 |
|
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