| Year |
Citation |
Score |
| 2023 |
Muhammad T, Houssen WE, Thomas L, Alexandru-Crivac CN, Gunasekera S, Jaspars M, Göransson U. Exploring the Limits of Cyanobactin Macrocyclase PatGmac: Cyclization of PawS-Derived Peptide Sunflower Trypsin Inhibitor-1 and Cyclotide Kalata B1. Journal of Natural Products. PMID 36917740 DOI: 10.1021/acs.jnatprod.2c01158 |
0.553 |
|
| 2021 |
Oluwabusola ET, Adebisi OO, Reyes F, Acquah KS, De La Cruz M, Mweetwa LL, Rajakulendran JE, Warner DF, Hai D, Ebel R, Jaspars M. Isolation and characterization of new phenolic siderophores with antimicrobial properties from sp. UIAU-6B. Beilstein Journal of Organic Chemistry. 17: 2390-2398. PMID 34621401 DOI: 10.3762/bjoc.17.156 |
0.301 |
|
| 2020 |
Jarmusch SA, Lagos-Susaeta D, Diab E, Salazar O, Asenjo JA, Ebel R, Jaspars M. Iron-meditated fungal starvation by lupine rhizosphere-associated and extremotolerant sp. S29 desferrioxamine production. Molecular Omics. PMID 33185220 DOI: 10.1039/d0mo00084a |
0.717 |
|
| 2020 |
Jarmusch SA, Feldmann I, Blank-Landeshammer B, Cortés-Albayay C, Castro JF, Andrews B, Asenjo JA, Sickmann A, Ebel R, Jaspars M. Cutting the Gordian knot: early and complete amino acid sequence confirmation of class II lasso peptides by HCD fragmentation. The Journal of Antibiotics. 73: 772-779. PMID 32908238 DOI: 10.1038/S41429-020-00369-Z |
0.742 |
|
| 2020 |
Oluwabusola ET, Tabudravu JN, Al Maqbali KS, Annang F, Pérez-Moreno G, Reyes F, Jaspars M. Antiparasitic activity of bromotyrosine alkaloids and new analogues isolated from the Fijian marine Sponge Aplysinella rhax. Chemistry & Biodiversity. PMID 32697400 DOI: 10.1002/Cbdv.202000335 |
0.38 |
|
| 2020 |
Acquah KS, Beukes DR, Warner DF, Meyers PR, Sunassee SN, Maglangit F, Deng H, Jaspars M, Gammon DW. Novel South African Rare Actinomycete Strain SK5: A Prolific Producer of Hydroxamate Siderophores Including New Dehydroxylated Congeners. Molecules (Basel, Switzerland). 25. PMID 32610457 DOI: 10.3390/Molecules25132979 |
0.35 |
|
| 2020 |
Abdel-Mageed WM, Lehri B, Jarmusch SA, Miranda K, Al-Wahaibi LH, Stewart HA, Jamieson AJ, Jaspars M, Karlyshev AV. Whole genome sequencing of four bacterial strains from South Shetland Trench revealing biosynthetic and environmental adaptation gene clusters. Marine Genomics. 100782. PMID 32387528 DOI: 10.1016/J.Margen.2020.100782 |
0.717 |
|
| 2020 |
Abdel-Mageed WM, Juhasz B, Lehri B, Alqahtani AS, Nouioui I, Pech-Puch D, Tabudravu JN, Goodfellow M, Rodríguez J, Jaspars M, Karlyshev AV. Whole Genome Sequence of MT1.1 Isolated from the Challenger Deep of the Mariana Trench Reveals Phenazine Biosynthesis Locus and Environmental Adaptation Factors. Marine Drugs. 18. PMID 32106586 DOI: 10.3390/Md18030131 |
0.383 |
|
| 2020 |
Harbottle JA, Petrie L, Ruhe M, Houssen WE, Jaspars M, Kolb AF. A cell-based assay system for activators of the environmental cell stress response. Analytical Biochemistry. 592: 113583. PMID 31945311 DOI: 10.1016/J.Ab.2020.113583 |
0.323 |
|
| 2020 |
Cortés-Albayay C, Jarmusch SA, Trusch F, Ebel R, Andrews BA, Jaspars M, Asenjo JA. Downsizing Class II Lasso Peptides: Genome Mining-Guided Isolation of Huascopeptin Containing the First Gly1-Asp7 Macrocycle. The Journal of Organic Chemistry. 85: 1661-1667. PMID 31931565 DOI: 10.1021/Acs.Joc.9B02231 |
0.747 |
|
| 2019 |
Gomez-Escribano JP, Castro JF, Razmilic V, Jarmusch SA, Saalbach G, Ebel R, Jaspars M, Andrews B, Asenjo JA, Bibb MJ. Heterologous expression of a cryptic gene cluster from C34 yields a novel lasso peptide, leepeptin. Applied and Environmental Microbiology. PMID 31562169 DOI: 10.1128/Aem.01752-19 |
0.741 |
|
| 2019 |
Martínez KA, Lauritano C, Druka D, Romano G, Grohmann T, Jaspars M, Martín J, Díaz C, Cautain B, de la Cruz M, Ianora A, Reyes F. Amphidinol 22, a New Cytotoxic and Antifungal Amphidinol from the Dinoflagellate . Marine Drugs. 17. PMID 31252576 DOI: 10.3390/Md17070385 |
0.362 |
|
| 2019 |
Abbasov ME, Alvariño R, Chaheine CM, Alonso E, Sánchez JA, Conner ML, Alfonso A, Jaspars M, Botana LM, Romo D. Simplified immunosuppressive and neuroprotective agents based on gracilin A. Nature Chemistry. 11: 342-350. PMID 30903037 DOI: 10.1038/S41557-019-0230-0 |
0.341 |
|
| 2019 |
Tabudravu JN, Pellissier L, Smith AJ, Subko K, Autréau C, Feussner K, Hardy D, Butler D, Kidd R, Milton EJ, Deng H, Ebel R, Salonna M, Gissi C, Montesanto F, ... ... Jaspars M, et al. LC-HRMS-Database Screening Metrics for Rapid Prioritization of Samples to Accelerate the Discovery of Structurally New Natural Products. Journal of Natural Products. PMID 30735391 DOI: 10.1021/Acs.Jnatprod.8B00575 |
0.336 |
|
| 2019 |
Tetevi GM, Kwain S, Mensah T, Camas AS, Camas M, Dofuor AK, Azerigyik FA, Oluwabusola E, Deng H, Jaspars M, Kyeremeh K. Paenidigyamycin G: 1-Acetyl-2,4-dimethyl-3-phenethyl-1H-imidazol-3-ium Molbank. 2019. DOI: 10.3390/M1094 |
0.391 |
|
| 2019 |
Kwain S, Tetevi GM, Mensah T, Camas AS, Camas M, Dofuor AK, Azerigyik FA, Deng H, Jaspars M, Kyeremeh K. Digyaindoleacid A: 2-(1-(4-Hydroxyphenyl)-3-oxobut-1-en-2-yloxy)-3-(1H-indol-3-yl)propanoic Acid, a Novel Indole Alkaloid Molbank. 2019. DOI: 10.3390/M1080 |
0.364 |
|
| 2019 |
Kyeremeh K, Kwain S, Tetevi GM, Camas AS, Camas M, Dofuor AK, Deng H, Jaspars M. α-D-glucopyranosyl-(1→2)-[6-O-(L-tryptophanyl)-β-D-fructofuranoside] Molbank. 2019. DOI: 10.3390/M1066 |
0.325 |
|
| 2019 |
Maglangit F, Tong MH, Jaspars M, Kyeremeh K, Deng H. Legonoxamines A-B, two new hydroxamate siderophores from the soil bacterium, Streptomyces sp. MA37 Tetrahedron Letters. 60: 75-79. DOI: 10.1016/J.Tetlet.2018.11.063 |
0.39 |
|
| 2018 |
Osei E, Kwain S, Mawuli GT, Anang AK, Owusu KB, Camas M, Camas AS, Ohashi M, Alexandru-Crivac CN, Deng H, Jaspars M, Kyeremeh K. Paenidigyamycin A, Potent Antiparasitic Imidazole Alkaloid from the Ghanaian sp. DE2SH. Marine Drugs. 17. PMID 30586918 DOI: 10.3390/Md17010009 |
0.303 |
|
| 2018 |
Tortorella E, Tedesco P, Palma Esposito F, January GG, Fani R, Jaspars M, de Pascale D. Antibiotics from Deep-Sea Microorganisms: Current Discoveries and Perspectives. Marine Drugs. 16. PMID 30274274 DOI: 10.3390/Md16100355 |
0.356 |
|
| 2018 |
Rateb ME, Ebel R, Jaspars M. Natural product diversity of actinobacteria in the Atacama Desert. Antonie Van Leeuwenhoek. 111: 1467-1477. PMID 29445902 DOI: 10.1007/S10482-018-1030-Z |
0.325 |
|
| 2018 |
Abdelkader MSA, Philippon T, Asenjo JA, Bull AT, Goodfellow M, Ebel R, Jaspars M, Rateb ME. Asenjonamides A-C, antibacterial metabolites isolated from Streptomyces asenjonii strain KNN 42.f from an extreme-hyper arid Atacama Desert soil. The Journal of Antibiotics. 71: 425-431. PMID 29362461 DOI: 10.1038/S41429-017-0012-0 |
0.329 |
|
| 2018 |
Oueis E, Stevenson H, Jaspars M, Westwood NJ, Naismith JH. Bypassing the proline/thiazoline requirement of the macrocyclase PatG. Chemical Communications (Cambridge, England). 53: 12274-12277. PMID 29090689 DOI: 10.1039/C7Cc06550G |
0.311 |
|
| 2017 |
Alexandru-Crivac CN, Umeobika C, Leikoski N, Jokela J, Rickaby KA, Grilo AM, Sjö P, Plowright AT, Idress M, Siebs E, Nneoyi-Egbe A, Wahlsten M, Sivonen K, Jaspars M, Trembleau L, et al. Cyclic peptide production using a macrocyclase with enhanced substrate promiscuity and relaxed recognition determinants. Chemical Communications (Cambridge, England). PMID 28905052 DOI: 10.1039/C7Cc05913B |
0.356 |
|
| 2017 |
Wakefield J, Hassan HM, Jaspars M, Ebel R, Rateb ME. Dual Induction of New Microbial Secondary Metabolites by Fungal Bacterial Co-cultivation. Frontiers in Microbiology. 8: 1284. PMID 28744271 DOI: 10.3389/Fmicb.2017.01284 |
0.373 |
|
| 2017 |
Booth J, Alexandru-Crivac CN, Rickaby KA, Nneoyiegbe AF, Umeobika U, McEwan AR, Trembleau L, Jaspars M, Houssen WE, Shalashilin DV. A Blind Test of Computational Technique for Predicting the Likelihood of Peptide Sequences to Cyclize. The Journal of Physical Chemistry Letters. 8: 2310-2315. PMID 28475844 DOI: 10.1021/Acs.Jpclett.7B00848 |
0.31 |
|
| 2017 |
Chervin J, Stierhof M, Tong MH, Peace D, Hansen KØ, Urgast DS, Andersen JH, Yu Y, Ebel R, Kyeremeh K, Paget V, Cimpan G, Wyk AV, Deng H, Jaspars M, et al. Targeted Dereplication of Microbial Natural Products by High-Resolution MS and Predicted LC Retention Time. Journal of Natural Products. PMID 28445069 DOI: 10.1021/Acs.Jnatprod.6B01035 |
0.388 |
|
| 2017 |
Alenezi FN, Rekik I, Chenari Bouket A, Luptakova L, Weitz HJ, Rateb ME, Jaspars M, Woodward S, Belbahri L. Increased Biological Activity of Aneurinibacillus migulanus Strains Correlates with the Production of New Gramicidin Secondary Metabolites. Frontiers in Microbiology. 8: 517. PMID 28439259 DOI: 10.3389/Fmicb.2017.00517 |
0.326 |
|
| 2017 |
Oueis E, Nardone B, Jaspars M, Westwood NJ, Naismith JH. Synthesis of Hybrid Cyclopeptides through Enzymatic Macrocyclization. Chemistryopen. 6: 11-14. PMID 28168143 DOI: 10.1002/Open.201600134 |
0.363 |
|
| 2017 |
Wichner D, Idris H, Houssen WE, McEwan AR, Bull AT, Asenjo JA, Goodfellow M, Jaspars M, Ebel R, Rateb ME. Isolation and anti-HIV-1 integrase activity of lentzeosides A-F from extremotolerant lentzea sp. H45, a strain isolated from a high-altitude Atacama Desert soil. The Journal of Antibiotics. 70: 448-453. PMID 27353167 DOI: 10.1038/Ja.2016.78 |
0.358 |
|
| 2017 |
Sonnenschein EC, Stierhof M, Goralczyk S, Vabre FM, Pellissier L, Hanssen KØ, Cruz Mdl, Díaz C, Witte Pd, Copmans D, Andersen JH, Hansen E, Kristoffersen V, Tormo JR, Ebel R, ... ... Jaspars M, et al. Pseudochelin A, a siderophore of Pseudoalteromonas piscicida S2040 Tetrahedron. 73: 2633-2637. DOI: 10.1016/J.Tet.2017.03.051 |
0.455 |
|
| 2016 |
Adaba RI, Mann G, Raab A, Houssen WE, McEwan AR, Thomas L, Tabudravu J, Naismith JH, Jaspars M. Accurate quantification of modified cyclic peptides without the need for authentic standards. Tetrahedron. 72: 8603-8609. PMID 32818002 DOI: 10.1016/J.Tet.2016.11.040 |
0.355 |
|
| 2016 |
Sánchez JA, Alfonso A, Rodriguez I, Alonso E, Cifuentes JM, Bermudez R, Rateb ME, Jaspars M, Houssen WE, Ebel R, Tabudravu J, Botana LM. Spongionella Secondary Metabolites, Promising Modulators of Immune Response through CD147 Receptor Modulation. Frontiers in Immunology. 7: 452. PMID 27822214 DOI: 10.3389/Fimmu.2016.00452 |
0.301 |
|
| 2016 |
Alonso E, Alvariño R, Leirós M, Tabudravu JN, Feussner K, Dam MA, Rateb ME, Jaspars M, Botana LM. Evaluation of the Antioxidant Activity of the Marine Pyrroloiminoquinone Makaluvamines. Marine Drugs. 14. PMID 27801775 DOI: 10.3390/Md14110197 |
0.325 |
|
| 2016 |
Brás NF, Ferreira P, Calixto AR, Jaspars M, Houssen W, Naismith JH, Fernandes PA, Ramos MJ. The Catalytic Mechanism of the Marine-Derived Macrocyclase PatGmac. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27389424 DOI: 10.1002/Chem.201601670 |
0.307 |
|
| 2016 |
Tedesco P, Maida I, Palma Esposito F, Tortorella E, Subko K, Ezeofor CC, Zhang Y, Tabudravu J, Jaspars M, Fani R, de Pascale D. Antimicrobial Activity of Monoramnholipids Produced by Bacterial Strains Isolated from the Ross Sea (Antarctica). Marine Drugs. 14. PMID 27128927 DOI: 10.3390/Md14050083 |
0.377 |
|
| 2016 |
Oueis E, Jaspars M, Westwood NJ, Naismith JH. Enzymatic Macrocyclization of 1,2,3-Triazole Peptide Mimetics. Angewandte Chemie (International Ed. in English). PMID 27059105 DOI: 10.1002/Anie.201601564 |
0.347 |
|
| 2016 |
Sánchez JA, Alfonso A, Leirós M, Alonso E, Rateb ME, Jaspars M, Houssen WE, Ebel R, Tabudravu J, Botana LM. Identification of Spongionella compounds as cyclosporine A mimics. Pharmacological Research. 107: 407-414. PMID 27041481 DOI: 10.1016/J.Phrs.2016.03.029 |
0.347 |
|
| 2016 |
Parajuli A, Kwak DH, Dalponte L, Leikoski N, Galica T, Umeobika U, Trembleau L, Bent A, Sivonen K, Wahlsten M, Wang H, Rizzi E, De Bellis G, Naismith J, Jaspars M, et al. A Unique Tryptophan C-Prenyltransferase from the Kawaguchipeptin Biosynthetic Pathway. Angewandte Chemie (International Ed. in English). PMID 26846478 DOI: 10.1002/Anie.201509920 |
0.341 |
|
| 2016 |
Alenezi FN, Rekik I, Bełka M, Ibrahim AF, Luptakova L, Jaspars M, Woodward S, Belbahri L. Strain-level diversity of secondary metabolism in the biocontrol species Aneurinibacillus migulanus. Microbiological Research. 182: 116-24. PMID 26686620 DOI: 10.1016/J.Micres.2015.10.007 |
0.349 |
|
| 2016 |
Stierhof M, Hansen KØ, Sharma M, Feussner K, Subko K, Díaz-Rullo FF, Isaksson J, Pérez-Victoria I, Clarke D, Hansen E, Jaspars M, Tabudravu JN. New cytotoxic callipeltins from the Solomon Island marine sponge Asteropus sp. Tetrahedron. 72: 6929-6934. DOI: 10.1016/J.Tet.2016.09.016 |
0.343 |
|
| 2015 |
Huang S, Elsayed SS, Lv M, Tabudravu J, Rateb ME, Gyampoh R, Kyeremeh K, Ebel R, Jaspars M, Deng Z, Yu Y, Deng H. Biosynthesis of Neocarazostatin A Reveals the Sequential Carbazole Prenylation and Hydroxylation in the Tailoring Steps. Chemistry & Biology. PMID 26670080 DOI: 10.1016/J.Chembiol.2015.10.012 |
0.324 |
|
| 2015 |
Elsayed SS, Trusch F, Deng H, Raab A, Prokes I, Busarakam K, Asenjo JA, Andrews BA, van West P, Bull AT, Goodfellow M, Yi Y, Ebel R, Jaspars M, Rateb ME. Chaxapeptin, a Lasso Peptide from Extremotolerant Streptomyces leeuwenhoekii Strain C58 from the Hyperarid Atacama Desert. The Journal of Organic Chemistry. PMID 26402731 DOI: 10.1021/Acs.Joc.5B01878 |
0.392 |
|
| 2015 |
Rateb ME, Zhai Y, Ehrner E, Rath CM, Wang X, Tabudravu J, Ebel R, Bibb M, Kyeremeh K, Dorrestein PC, Hong K, Jaspars M, Deng H. Legonaridin, a new member of linaridin RiPP from a Ghanaian Streptomyces isolate. Organic & Biomolecular Chemistry. 13: 9585-92. PMID 26256511 DOI: 10.1039/C5Ob01269D |
0.382 |
|
| 2015 |
Huang S, Tabudravu J, Elsayed SS, Travert J, Peace D, Tong MH, Kyeremeh K, Kelly SM, Trembleau L, Ebel R, Jaspars M, Yu Y, Deng H. Discovery of a Single Monooxygenase that Catalyzes Carbamate Formation and Ring Contraction in the Biosynthesis of the Legonmycins. Angewandte Chemie (International Ed. in English). PMID 26206556 DOI: 10.1002/Anie.201502902 |
0.331 |
|
| 2015 |
Koehnke J, Mann G, Bent AF, Ludewig H, Shirran S, Botting C, Lebl T, Houssen WE, Jaspars M, Naismith JH. Structural analysis of leader peptide binding enables leader-free cyanobactin processing. Nature Chemical Biology. 11: 558-63. PMID 26098679 DOI: 10.1038/Nchembio.1841 |
0.321 |
|
| 2015 |
Hassan MHA, Rateb ME, Hetta M, Abdelaziz TA, Sleim MA, Jaspars M, Mohammed R. Scalarane sesterterpenes from the Egyptian Red Sea sponge Phyllospongia lamellosa Tetrahedron. 71: 577-583. DOI: 10.1016/J.Tet.2014.12.035 |
0.365 |
|
| 2014 |
Quintana J, Bayona LM, Castellanos L, Puyana M, Camargo P, Aristizábal F, Edwards C, Tabudravu JN, Jaspars M, Ramos FA. Almiramide D, cytotoxic peptide from the marine cyanobacterium Oscillatoria nigroviridis. Bioorganic & Medicinal Chemistry. 22: 6789-95. PMID 25468043 DOI: 10.1016/J.Bmc.2014.10.039 |
0.359 |
|
| 2014 |
Koehnke J, Bent AF, Houssen WE, Mann G, Jaspars M, Naismith JH. The structural biology of patellamide biosynthesis. Current Opinion in Structural Biology. 29: 112-21. PMID 25460274 DOI: 10.1016/J.Sbi.2014.10.006 |
0.366 |
|
| 2014 |
Houssen WE, Bent AF, McEwan AR, Pieiller N, Tabudravu J, Koehnke J, Mann G, Adaba RI, Thomas L, Hawas UW, Liu H, Schwarz-Linek U, Smith MC, Naismith JH, Jaspars M. An efficient method for the in vitro production of azol(in)e-based cyclic peptides. Angewandte Chemie (International Ed. in English). 53: 14171-4. PMID 25331823 DOI: 10.1002/Anie.201408082 |
0.363 |
|
| 2014 |
Kyeremeh K, Acquah KS, Camas M, Tabudravu J, Houssen W, Deng H, Jaspars M. Butrepyrazinone, a new pyrazinone with an unusual methylation pattern from a Ghanaian Verrucosispora sp. K51G. Marine Drugs. 12: 5197-208. PMID 25325732 DOI: 10.3390/Md12105197 |
0.36 |
|
| 2014 |
Jaspars M. The origins of cyanobactin chemistry and biology. Chemical Communications (Cambridge, England). 50: 10174-6. PMID 25068542 DOI: 10.1039/C3Cc49252D |
0.353 |
|
| 2014 |
Rateb ME, Hassan HM, Arafa el-SA, Jaspars M, Ebel R. Decorosides A and B, cytotoxic flavonoid glycosides from the leaves of Rhododendron decorum. Natural Product Communications. 9: 473-6. PMID 24868859 DOI: 10.1177/1934578X1400900410 |
0.376 |
|
| 2014 |
Tadesse M, Svenson J, Sepčić K, Trembleau L, Engqvist M, Andersen JH, Jaspars M, Stensvåg K, Haug T. Isolation and synthesis of pulmonarins A and B, acetylcholinesterase inhibitors from the colonial ascidian Synoicum pulmonaria. Journal of Natural Products. 77: 364-9. PMID 24547899 DOI: 10.1021/Np401002S |
0.329 |
|
| 2014 |
Kyeremeh K, Acquah KS, Sazak A, Houssen W, Tabudravu J, Deng H, Jaspars M. Butremycin, the 3-hydroxyl derivative of ikarugamycin and a protonated aromatic tautomer of 5'-methylthioinosine from a Ghanaian Micromonospora sp. K310. Marine Drugs. 12: 999-1012. PMID 24534843 DOI: 10.3390/Md12020999 |
0.389 |
|
| 2014 |
Wagner M, Abdel-Mageed WM, Ebel R, Bull AT, Goodfellow M, Fiedler HP, Jaspars M. Dermacozines H-J isolated from a deep-sea strain of Dermacoccus abyssi from Mariana Trench sediments. Journal of Natural Products. 77: 416-20. PMID 24499261 DOI: 10.1021/Np400952D |
0.365 |
|
| 2014 |
Jaspars M, Challis G. Microbiology: a talented genus. Nature. 506: 38-9. PMID 24476822 DOI: 10.1038/Nature13049 |
0.338 |
|
| 2014 |
Leirós M, Sánchez JA, Alonso E, Rateb ME, Houssen WE, Ebel R, Jaspars M, Alfonso A, Botana LM. Spongionella secondary metabolites protect mitochondrial function in cortical neurons against oxidative stress. Marine Drugs. 12: 700-18. PMID 24473170 DOI: 10.3390/Md12020700 |
0.301 |
|
| 2014 |
Folmer F, Basavaraju U, Jaspars M, Hold G, El-Omar E, Dicato M, Diederich M. Anticancer effects of bioactive berry compounds Phytochemistry Reviews. 13: 295-322. DOI: 10.1007/S11101-013-9319-Z |
0.307 |
|
| 2013 |
Chen C, Liu X, Abdel-Mageed WM, Guo H, Hou W, Jaspars M, Li L, Xie F, Ren B, Wang Q, Dai H, Song F, Zhang L. Nivetetracyclates A and B: novel compounds isolated from Streptomyces niveus. Organic Letters. 15: 5762-5. PMID 24160456 DOI: 10.1021/Ol4027733 |
0.384 |
|
| 2013 |
Bent AF, Koehnke J, Houssen WE, Smith MC, Jaspars M, Naismith JH. Structure of PatF from Prochloron didemni. Acta Crystallographica. Section F, Structural Biology and Crystallization Communications. 69: 618-23. PMID 23722837 DOI: 10.1107/S1744309113012931 |
0.314 |
|
| 2013 |
Arnison PG, Bibb MJ, Bierbaum G, Bowers AA, Bugni TS, Bulaj G, Camarero JA, Campopiano DJ, Challis GL, Clardy J, Cotter PD, Craik DJ, Dawson M, Dittmann E, Donadio S, ... ... Jaspars M, et al. Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature. Natural Product Reports. 30: 108-60. PMID 23165928 DOI: 10.1039/C2Np20085F |
0.606 |
|
| 2013 |
Rateb ME, Hallyburton I, Houssen WE, Bull AT, Goodfellow M, Santhanam R, Jaspars M, Ebel R. Induction of diverse secondary metabolites in Aspergillus fumigatus by microbial co-culture Rsc Advances. 3: 14444-14450. DOI: 10.1039/C3Ra42378F |
0.367 |
|
| 2013 |
Arnison PG, Bibb MJ, Bierbaum G, Bowers AA, Bugni TS, Bulaj G, Camarero JA, Campopiano DJ, Challis GL, Clardy J, Cotter PD, Craik DJ, Dawson M, Dittmann E, Donadio S, ... ... Jaspars M, et al. Erratum: Ribosomally synthesized and post-translationally modified peptide natural products: Overview and recommendations for a universal nomenclature (Natural Product Reports (2013) 30 (108-160) DOI:10.1039/C2NP20085F) Natural Product Reports. 30: 1568-1568. DOI: 10.1039/C3Np90040A |
0.59 |
|
| 2013 |
Wang X, Tabudravu JN, Jaspars M, Deng H. Tianchimycins A–B, 16-membered macrolides from the rare actinomycete Saccharothrix xinjiangensis Tetrahedron. 69: 6060-6064. DOI: 10.1016/J.Tet.2013.05.094 |
0.383 |
|
| 2012 |
Houssen WE, Koehnke J, Zollman D, Vendome J, Raab A, Smith MC, Naismith JH, Jaspars M. The discovery of new cyanobactins from Cyanothece PCC 7425 defines a new signature for processing of patellamides. Chembiochem : a European Journal of Chemical Biology. 13: 2683-9. PMID 23169461 DOI: 10.1002/Cbic.201200661 |
0.374 |
|
| 2012 |
Koehnke J, Bent A, Houssen WE, Zollman D, Morawitz F, Shirran S, Vendome J, Nneoyiegbe AF, Trembleau L, Botting CH, Smith MC, Jaspars M, Naismith JH. The mechanism of patellamide macrocyclization revealed by the characterization of the PatG macrocyclase domain. Nature Structural & Molecular Biology. 19: 767-72. PMID 22796963 DOI: 10.1038/Nsmb.2340 |
0.374 |
|
| 2012 |
Qin Z, McNee D, Gleisner H, Raab A, Kyeremeh K, Jaspars M, Krupp E, Deng H, Feldmann J. Fluorine speciation analysis using reverse phase liquid chromatography coupled off-line to continuum source molecular absorption spectrometry (CS-MAS): identification and quantification of novel fluorinated organic compounds in environmental and biological samples. Analytical Chemistry. 84: 6213-9. PMID 22686502 DOI: 10.1021/Ac301201Y |
0.32 |
|
| 2012 |
Houssen WE, Jaspars M. Isolation of marine natural products. Methods in Molecular Biology (Clifton, N.J.). 864: 367-92. PMID 22367904 DOI: 10.1007/978-1-61779-624-1_14 |
0.363 |
|
| 2012 |
Ibraheim ZZ, Abdel-Mageed WM, Dai H, Guo H, Zhang L, Jaspars M. Antimicrobial antioxidant daucane sesquiterpenes from Ferula hermonis Boiss. Phytotherapy Research : Ptr. 26: 579-86. PMID 21953875 DOI: 10.1002/Ptr.3609 |
0.381 |
|
| 2012 |
Schumacher M, Wilson N, Tabudravu JN, Edwards C, Lawton LA, Motti C, Wright AD, Diederich M, Jaspars M. New nodulopeptins from Nodularia spumigena KAC 66 Tetrahedron. 68: 1622-1628. DOI: 10.1016/J.Tet.2011.11.056 |
0.381 |
|
| 2012 |
Zovko A, Gabrič MV, Sepčić K, Pohleven F, Jaklič D, Gunde-Cimerman N, Lu Z, Edrada-Ebel R, Houssen WE, Mancini I, Defant A, Jaspars M, Turk T. Antifungal and antibacterial activity of 3-alkylpyridinium polymeric analogs of marine toxins International Biodeterioration & Biodegradation. 68: 71-77. DOI: 10.1016/J.Ibiod.2011.10.014 |
0.341 |
|
| 2011 |
Rateb ME, Houssen WE, Harrison WT, Deng H, Okoro CK, Asenjo JA, Andrews BA, Bull AT, Goodfellow M, Ebel R, Jaspars M. Diverse metabolic profiles of a Streptomyces strain isolated from a hyper-arid environment. Journal of Natural Products. 74: 1965-71. PMID 21879726 DOI: 10.1021/Np200470U |
0.369 |
|
| 2011 |
Rateb ME, Houssen WE, Arnold M, Abdelrahman MH, Deng H, Harrison WT, Okoro CK, Asenjo JA, Andrews BA, Ferguson G, Bull AT, Goodfellow M, Ebel R, Jaspars M. Chaxamycins A-D, bioactive ansamycins from a hyper-arid desert Streptomyces sp. Journal of Natural Products. 74: 1491-9. PMID 21553813 DOI: 10.1021/Np200320U |
0.38 |
|
| 2011 |
Tadesse M, Tabudravu JN, Jaspars M, Strøm MB, Hansen E, Andersen JH, Kristiansen PE, Haug T. The antibacterial ent-eusynstyelamide B and eusynstyelamides D, E, and F from the Arctic bryozoan Tegella cf. spitzbergensis. Journal of Natural Products. 74: 837-41. PMID 21370896 DOI: 10.1021/Np100499C |
0.323 |
|
| 2011 |
Tadesse M, Svenson J, Jaspars M, Strøm MB, Abdelrahman MH, Andersen JH, Hansen E, Kristiansen PE, Stensvåg K, Haug T. Synoxazolidinone C; a bicyclic member of the synoxazolidinone family with antibacterial and anticancer activities Tetrahedron Letters. 52: 1804-1806. DOI: 10.1016/J.Tetlet.2011.02.027 |
0.353 |
|
| 2010 |
Houssen WE, Lu Z, Edrada-Ebel R, Chatzi C, Tucker SJ, Sepčić K, Turk T, Zovko A, Shen S, Mancini I, Scott RH, Jaspars M. Chemical synthesis and biological activities of 3-alkyl pyridinium polymeric analogues of marine toxins. Journal of Chemical Biology. 3: 113-25. PMID 21326630 DOI: 10.1007/S12154-010-0036-4 |
0.301 |
|
| 2010 |
Tadesse M, Strøm MB, Svenson J, Jaspars M, Milne BF, Tørfoss V, Andersen JH, Hansen E, Stensvåg K, Haug T. Synoxazolidinones A and B: novel bioactive alkaloids from the ascidian Synoicum pulmonaria. Organic Letters. 12: 4752-5. PMID 20883040 DOI: 10.1021/Ol101707U |
0.386 |
|
| 2010 |
Gross L, Mohn F, Moll N, Meyer G, Ebel R, Abdel-Mageed WM, Jaspars M. Organic structure determination using atomic-resolution scanning probe microscopy. Nature Chemistry. 2: 821-5. PMID 20861896 DOI: 10.1038/Nchem.765 |
0.311 |
|
| 2010 |
Folmer F, Jaspars M, Schumacher M, Dicato M, Diederich M. Marine natural products targeting phospholipases A2. Biochemical Pharmacology. 80: 1793-800. PMID 20833149 DOI: 10.1016/J.Bcp.2010.08.024 |
0.319 |
|
| 2010 |
Houssen WE, Wright SH, Kalverda AP, Thompson GS, Kelly SM, Jaspars M. Solution structure of the leader sequence of the patellamide precursor peptide, PatE1-34. Chembiochem : a European Journal of Chemical Biology. 11: 1867-73. PMID 20715266 DOI: 10.1002/Cbic.201000305 |
0.307 |
|
| 2010 |
Houssen WE, Jaspars M. Azole-based cyclic peptides from the sea squirt Lissoclinum patella: old scaffolds, new avenues. Chembiochem : a European Journal of Chemical Biology. 11: 1803-15. PMID 20632432 DOI: 10.1002/Cbic.201000230 |
0.327 |
|
| 2010 |
Abdel-Mageed WM, Milne BF, Wagner M, Schumacher M, Sandor P, Pathom-aree W, Goodfellow M, Bull AT, Horikoshi K, Ebel R, Diederich M, Fiedler HP, Jaspars M. Dermacozines, a new phenazine family from deep-sea dermacocci isolated from a Mariana Trench sediment. Organic & Biomolecular Chemistry. 8: 2352-62. PMID 20448892 DOI: 10.1039/C001445A |
0.366 |
|
| 2010 |
Abdel-Mageed WM, Ebel R, Valeriote FA, Jaspars M. Laurefurenynes A–F, new Cyclic Ether Acetogenins from a Marine Red Alga, Laurencia sp. Tetrahedron. 66: 2855-2862. DOI: 10.1016/J.Tet.2010.02.041 |
0.39 |
|
| 2010 |
Folmer F, Jaspars M, Dicato M, Diederich M. Photosynthetic marine organisms as a source of anticancer compounds Phytochemistry Reviews. 9: 557-579. DOI: 10.1007/S11101-010-9200-2 |
0.353 |
|
| 2010 |
DAVIS AP, JASPARS M. ChemInform Abstract: Super-Acid Catalysed Addition of Allylsilanes to Carbonyl Compounds; Synthetic and Mechanistic Aspects. Cheminform. 23: no-no. DOI: 10.1002/chin.199248075 |
0.476 |
|
| 2010 |
DAVIS AP, JASPARS M. ChemInform Abstract: Catalysis of the Addition of Allyltrimethylsilane to Aldehydes by Silylating Agents. Me3SiB(OTf)4, a New “Supersilylating” Reagent. Cheminform. 23: no-no. DOI: 10.1002/chin.199230061 |
0.427 |
|
| 2010 |
DAVIS AP, JASPARS M. ChemInform Abstract: Superacid Catalysis of the Addition of Allylsilanes to Carbonyl Compounds. Cheminform. 22: no-no. DOI: 10.1002/chin.199106132 |
0.474 |
|
| 2010 |
Houssen WE, Jaspars M. Inside Cover: Azole-Based Cyclic Peptides from the Sea Squirt Lissoclinum Patella: Old Scaffolds, New Avenues (ChemBioChem 13/2010) Chembiochem. 11: 1790-1790. DOI: 10.1002/Cbic.201090062 |
0.326 |
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| 2009 |
Rateb ME, Houssen WE, Schumacher M, Harrison WT, Diederich M, Ebel R, Jaspars M. Bioactive diterpene derivatives from the marine sponge Spongionella sp. Journal of Natural Products. 72: 1471-6. PMID 19601607 DOI: 10.1021/Np900233C |
0.381 |
|
| 2009 |
Solano G, Motti CA, Jaspars M. New iodotyramine derivatives from Didemnum rubeum Tetrahedron. 65: 7482-7486. DOI: 10.1016/J.Tet.2009.07.002 |
0.361 |
|
| 2008 |
El-Gendy MM, Hawas UW, Jaspars M. Novel bioactive metabolites from a marine derived bacterium Nocardia sp. ALAA 2000. The Journal of Antibiotics. 61: 379-86. PMID 18667786 DOI: 10.1038/Ja.2008.53 |
0.413 |
|
| 2008 |
Folmer F, Harrison WT, Tabudravu JN, Jaspars M, Aalbersberg W, Feussner K, Wright AD, Dicato M, Diederich M. NF-kappaB-inhibiting naphthopyrones from the Fijian echinoderm Comanthus parvicirrus. Journal of Natural Products. 71: 106-11. PMID 18088098 DOI: 10.1021/Np070290Y |
0.311 |
|
| 2008 |
Abdel-Mageed MW, Jaspars M, Goodfellow M, Bull A, Horikoshi K, Milne BF. New heteroatomatic compounds from the deep Planta Medica. 74. DOI: 10.1055/S-0028-1084504 |
0.343 |
|
| 2007 |
Dunlap WC, Battershill CN, Liptrot CH, Cobb RE, Bourne DG, Jaspars M, Long PF, Newman DJ. Biomedicinals from the phytosymbionts of marine invertebrates: a molecular approach. Methods (San Diego, Calif.). 42: 358-76. PMID 17560324 DOI: 10.1016/J.Ymeth.2007.03.001 |
0.374 |
|
| 2007 |
Starcevic A, Jaspars M, Cullum J, Hranueli D, Long PF. Predicting the nature and timing of epimerisation on a modular polyketide synthase. Chembiochem : a European Journal of Chemical Biology. 8: 28-31. PMID 17133646 DOI: 10.1002/Cbic.200600399 |
0.314 |
|
| 2007 |
Shoeb M, MacManus SM, Jaspars M, Kong-Thoo-Lin P, Nahar L, Celik S, Sarker SD. Bioactivity of two Turkish endemic Centaurea species, and their major constituents Revista Brasileira De Farmacognosia-Brazilian Journal of Pharmacognosy. 17: 155-159. DOI: 10.1590/S0102-695X2007000200003 |
0.313 |
|
| 2007 |
Hawas UW, El-Gendy MM, Jaspars M. Novel bioactive bacterial metabolites from a marine derived bacterium Nocardia Sp. Merv 21695 Planta Medica. 73. DOI: 10.1055/S-2007-986976 |
0.327 |
|
| 2007 |
Shoeb M, Jaspars M, MacManus SM, Celik S, Nahar L, Kong-Thoo-Lin P, Sarker SD. Anti-colon cancer potential of phenolic compounds from the aerial parts of Centaurea gigantea (Asteraceae) Journal of Natural Medicines. 61: 164-169. DOI: 10.1007/S11418-006-0117-4 |
0.347 |
|
| 2006 |
Shoeb M, MacManus SM, Kumarasamy Y, Jaspars M, Nahar L, Thoo-Lin PK, Nazemiyeh H, Sarker SD. Americanin, a bioactive dibenzylbutyrolactone lignan, from the seeds of Centaurea americana. Phytochemistry. 67: 2370-2375. PMID 16996096 DOI: 10.1016/J.Phytochem.2006.08.012 |
0.367 |
|
| 2006 |
Dunlap WC, Jaspars M, Hranueli D, Battershill CN, Peri?-Concha N, Zucko J, Wright SH, Long PF. New methods for medicinal chemistry--universal gene cloning and expression systems for production of marine bioactive metabolites. Current Medicinal Chemistry. 13: 697-710. PMID 16529560 DOI: 10.2174/092986706776055643 |
0.318 |
|
| 2006 |
Milne BF, Long PF, Starcevic A, Hranueli D, Jaspars M. Spontaneity in the patellamide biosynthetic pathway. Organic & Biomolecular Chemistry. 4: 631-8. PMID 16467937 DOI: 10.1039/B515938E |
0.351 |
|
| 2006 |
Kumarasamy Y, Cox PJ, Jaspars M, Nahar L, Sarker SD. Bioactivity of Hirsutanolol, Oregonin and Genkwanin, Isolated from the Seeds of Alnus Glutinosa (Betulaceae): Natural Product Communications. 1. DOI: 10.1177/1934578X0600100808 |
0.314 |
|
| 2006 |
Shoeb M, MacManus SM, Jaspars M, Trevidu JN, Nahar L, Kong-Thoo-Lin P, Sarker SD. Montamine, a unique dimeric indole alkaloid, from the seeds of Centaurea montana (Asteraceae), and its in vitro cytotoxic activity against the CaCo2 colon cancer cells Tetrahedron. 62: 11172-11177. DOI: 10.1016/J.Tet.2006.09.020 |
0.322 |
|
| 2006 |
Kyeremeh K, Baddeley TC, Stein BK, Jaspars M. A homologous series of eunicellin-based diterpenes from Acalycigorgia sp. characterised by tandem mass spectrometry Tetrahedron. 62: 8770-8778. DOI: 10.1016/J.Tet.2006.06.102 |
0.313 |
|
| 2005 |
Houssen WE, Jaspars M. 4-Hydroxybenzoyl derivative from the aqueous extract of the hydroid Campanularia sp. Journal of Natural Products. 68: 453-455. PMID 15787459 DOI: 10.1021/Np049666N |
0.38 |
|
| 2005 |
Tabudravu JN, Jaspars M. Anticancer activities of constituents of kava (Piper methysticum) The South Pacific Journal of Natural and Applied Sciences. 23: 26-29. DOI: 10.1071/Sp05005 |
0.346 |
|
| 2005 |
Shoeb M, Celik S, Jaspars M, Kumarasamy Y, MacManus SM, Nahar L, Thoo-Lin PK, Sarker SD. Isolation, structure elucidation and bioactivity of schischkiniin, a unique indole alkaloid from the seeds of Centaurea schischkinii Tetrahedron. 61: 9001-9006. DOI: 10.1016/J.Tet.2005.07.047 |
0.374 |
|
| 2004 |
Hansen HR, Raab A, Jaspars M, Milne BF, Feldmann J. Sulfur-containing arsenical mistaken for dimethylarsinous acid [DMA(III)] and identified as a natural metabolite in urine: major implications for studies on arsenic metabolism and toxicity. Chemical Research in Toxicology. 17: 1086-91. PMID 15310240 DOI: 10.1021/Tx049978Q |
0.309 |
|
| 2004 |
Hansen HR, Pickford R, Thomas-Oates J, Jaspars M, Feldmann J. 2-Dimethylarsinothioyl acetic acid identified in a biological sample: the first occurrence of a mammalian arsinothioyl metabolite. Angewandte Chemie. 43: 337-340. PMID 14705091 DOI: 10.1002/Anie.200352740 |
0.353 |
|
| 2004 |
Dzeha T, Jaspars M, Tabudravu JN. Clionasterol, a triterpenoid from the Kenyan marine green macroalga halimeda macroloba Western Indian Ocean Journal of Marine Science. 2: 157-161. DOI: 10.4314/Wiojms.V2I2.28436 |
0.377 |
|
| 2004 |
Kumarasamy Y, Byres M, Cox PJ, Delazar A, Jaspars M, Nahar L, Shoeb M, Sarker SD. Isolation, structure elucidation, and biological activity of flavone 6-C-glycosides from Alliaria petiolata Chemistry of Natural Compounds. 40: 122-128. DOI: 10.1023/B:Conc.0000033926.72396.41 |
0.325 |
|
| 2003 |
Shoeb M, Jaspars M. Chlorinated C12 fatty acid metabolites from the red alga Gracilaria verrucosa. Journal of Natural Products. 66: 1509-1511. PMID 14640530 DOI: 10.1021/Np0302246 |
0.344 |
|
| 2003 |
Kumarasamy Y, Nahar L, Cox PJ, Jaspars M, Sarker SD. Bioactivity of secoiridoid glycosides from Centaurium erythraea Phytomedicine. 10: 344-347. PMID 12809366 DOI: 10.1078/094471103322004857 |
0.374 |
|
| 2003 |
Kumarasamy Y, Cox PJ, Jaspars M, Nahar L, Sarker SD. Cyanogenic glycosids from Prunus spinosa (Rosaceae) Biochemical Systematics and Ecology. 31: 1063-1065. DOI: 10.1016/S0305-1978(03)00063-2 |
0.314 |
|
| 2003 |
Kumarasamy Y, Cox PJ, Jaspars M, Nahar L, Sarker SD. Isolation, structure elucidation and biological activity of hederacine A and B, two unique alkaloids from Glechoma hederaceae Tetrahedron. 59: 6403-6407. DOI: 10.1016/S0040-4020(03)01093-7 |
0.367 |
|
| 2002 |
Tabudravu JN, Jaspars M. Purealidin S and purpuramine J, bromotyrosine alkaloids from the Fijian marine sponge Druinella sp. Journal of Natural Products. 65: 1798-1801. PMID 12502317 DOI: 10.1021/Np020275N |
0.376 |
|
| 2002 |
Tabudravu JN, Eijsink VGH, Gooday GW, Jaspars M, Komander D, Legg M, Synstad B, Aalten DMFv. Psammaplin A, a chitinase inhibitor isolated from the fijian marine sponge Aplysinella rhax Bioorganic & Medicinal Chemistry. 10: 1123-1128. PMID 11836123 DOI: 10.1016/S0968-0896(01)00372-8 |
0.36 |
|
| 2002 |
Tabudravu JN, Morris LA, Bosch JJKd, Jaspars M. Axinellin C, a proline-rich cyclic octapeptide isolated from the Fijian marine sponge Stylotella aurantium Tetrahedron. 58: 7863-7868. DOI: 10.1016/S0040-4020(02)00898-0 |
0.36 |
|
| 2001 |
Sarker SD, Laird A, Nahar L, Kumarasamy Y, Jaspars M. Indole alkaloids from the seeds of Centaurea cyanus (Asteraceae). Phytochemistry. 57: 1273-1276. PMID 11454358 DOI: 10.1016/S0031-9422(01)00084-X |
0.357 |
|
| 2001 |
Tabudravu JN, Jaspars M. Stelliferin riboside, a triterpene monosaccharide isolated from the Fijian sponge Geodia globostellifera. Journal of Natural Products. 64: 813-815. PMID 11421753 DOI: 10.1021/Np010019V |
0.327 |
|
| 2001 |
Tabudravu JN, Morris LA, Bosch JJKd, Jaspars M. Wainunuamide, a histidine-containing proline-rich cyclic heptapeptide isolated from the Fijian marine sponge Stylotella aurantium Tetrahedron Letters. 42: 9273-9276. DOI: 10.1016/S0040-4039(01)01993-1 |
0.366 |
|
| 2000 |
McLaggan D, Rufino H, Jaspars M, Booth IR. Glutathione-dependent conversion of N-ethylmaleimide to the maleamic acid by Escherichia coli: an intracellular detoxification process. Applied and Environmental Microbiology. 66: 1393-1399. PMID 10742217 DOI: 10.1128/Aem.66.4.1393-1399.2000 |
0.309 |
|
| 2000 |
Morris LA, Bosch JJKvd, Versluis K, Thompson GS, Jaspars M. Structure determination and MSn analysis of two new lissoclinamides isolated from the Indo-Pacific ascidian Lissoclinum patella: NOE restrained molecular dynamics confirms the absolute stereochemistry derived by degradative methods Tetrahedron. 56: 8345-8353. DOI: 10.1016/S0040-4020(00)00746-8 |
0.351 |
|
| 1999 |
Lawton LA, Morris LA, Jaspars M. A Bioactive Modified Peptide, Aeruginosamide, Isolated From The Cyanobacterium Microcystis Aeruginosa Journal of Organic Chemistry. 64: 5329-5332. DOI: 10.1021/Jo990247I |
0.35 |
|
| 1999 |
Lawton LA, Robertson PKJ, Cornish BJPA, Jaspars M. Detoxification of microcystins (cyanobacterial hepatotoxins) using TiO2 photocatalytic oxidation Environmental Science & Technology. 33: 771-775. DOI: 10.1021/Es9806682 |
0.318 |
|
| 1998 |
Morris LA, Christie EM, Jaspars M, Ofwegen LPV. A Bioactive Secosterol with an Unusual A- and B-Ring Oxygenation Pattern Isolated from an Indonesian Soft Coral Lobophytum sp. Journal of Natural Products. 61: 538-541. PMID 9584407 DOI: 10.1021/Np9705118 |
0.338 |
|
| 1998 |
Morris LA, Jaspars M, Adamson K, Woods S, Wallace HM. The capnellenes revisited: New structures and new biological activity Tetrahedron. 54: 12953-12958. DOI: 10.1016/S0040-4020(98)00784-4 |
0.371 |
|
| 1997 |
Jaspars M, Jackson E, Lobkovsky E, Clardy J, Diaz MC, Crews P. Using scalarane sesterterpenes to examine a sponge taxonomic anomaly. Journal of Natural Products. 60: 556-61. PMID 9214728 DOI: 10.1021/np960147x |
0.477 |
|
| 1995 |
Jaspars M, Horton PA, Madrid LH, Crews P. The cyclorenierins, sesquiterpenoid quinols from the sponge Haliclona sp. collected in Vanuatu. Journal of Natural Products. 58: 609-12. PMID 7623039 DOI: 10.1021/Np50118A023 |
0.534 |
|
| 1994 |
Alvi KA, Jaspars M, Crews P, Strulovici B, Oto E. Penazetidine A, an alkaloid inhibitor of protein kinase C Bioorganic and Medicinal Chemistry Letters. 4: 2447-2450. DOI: 10.1016/S0960-894X(01)80407-8 |
0.526 |
|
| 1994 |
Jaspars M, Crews P. A triterpene tetrasaccharide, formoside, from the Caribbean Choristida sponge Erylus formosus Tetrahedron Letters. 35: 7501-7504. DOI: 10.1016/S0040-4039(00)78328-6 |
0.522 |
|
| 1994 |
Jaspars M, Rali T, Laney M, Schatzman RC, Diaz MC, Schmitz FJ, Pordesimo EO, Crews P. The search for inosine 5′-Phosphate dehydrogenase (IMPDH) inhibitors from marine sponges. Evaluation of the bastadin alkaloids Tetrahedron. 50: 7367-7374. DOI: 10.1016/S0040-4020(01)90467-3 |
0.57 |
|
| 1994 |
Crews P, Cheng XC, Adamczeski M, Rodríguez J, Jaspars M, Schmitz FJ, Traeger SC, Pordesimo EO. 1,2,3,4-tetrahydro-8-hydroxymanzamines, alkaloids from two different haplosclerid sponges Tetrahedron. 50: 13567-13574. DOI: 10.1016/S0040-4020(01)85671-4 |
0.55 |
|
| 1992 |
Davis AP, Jaspars M. Super-acid catalysed addition of allylsilanes to carbonyl compounds; synthetic and mechanistic aspects Journal of the Chemical Society-Perkin Transactions 1. 2111-2118. DOI: 10.1039/P19920002111 |
0.511 |
|
| 1992 |
Davis AP, Jaspars M. Catalysis of the Addition of Allyltrimethylsilane to Aldehydes by Silylating Agents. Me3SiB(OTf)4, a New,‘Supersilylating’ Reagent Angewandte Chemie International Edition in English. 31: 470-471. DOI: 10.1002/Anie.199204701 |
0.487 |
|
| 1992 |
Davis AP, Jaspars M. Silylierungsmittel-katalysierte Addition von Allyltrimethylsilan an Aldehyde: Me3SiB(OTf)4, ein äußerst wirksames Silylierungsreagens Angewandte Chemie. 104: 475-477. DOI: 10.1002/Ange.19921040427 |
0.472 |
|
| 1990 |
Davis AP, Jaspars M. Superacid catalysis of the addition of allysilanes to carbonyl compounds Journal of the Chemical Society, Chemical Communications. 1176-1178. DOI: 10.1039/C39900001176 |
0.487 |
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