Year |
Citation |
Score |
2021 |
Babaee S, Zarei M, Zolfigol MA, Khazalpour S, Hasani M, Rinner U, Schirhagl R, Norouzi N, Rostamnia S. Synthesis of biological based hennotannic acid-based salts over porous bismuth coordination polymer with phosphorous acid tags. Rsc Advances. 11: 2141-2157. PMID 35424185 DOI: 10.1039/d0ra06674e |
0.368 |
|
2021 |
Wicks C, Hudlicky T, Rinner U. Morphine alkaloids: History, biology, and synthesis. The Alkaloids. Chemistry and Biology. 86: 145-342. PMID 34565506 DOI: 10.1016/bs.alkal.2021.04.001 |
0.398 |
|
2019 |
Nowikow C, Fuerst R, Kauderer M, Dank C, Schmid W, Hajduch M, Rehulka J, Gurska S, Mokshyna O, Polishchuk P, Zupkó I, Dzubak P, Rinner U. Synthesis and biological evaluation of cis-restrained carbocyclic combretastatin A-4 analogs: Influence of the ring size and saturation on cytotoxic properties. Bioorganic & Medicinal Chemistry. 115032. PMID 31401010 DOI: 10.1016/J.Bmc.2019.07.048 |
0.4 |
|
2017 |
Rinner U. Galbulimima Alkaloids. The Alkaloids. Chemistry and Biology. 78: 109-166. PMID 28838427 DOI: 10.1016/Bs.Alkal.2017.05.001 |
0.439 |
|
2017 |
Al-Hamdi AM, Rinner U, Sillanpää M. Tin dioxide as a photocatalyst for water treatment: A review Process Safety and Environmental Protection. 107: 190-205. DOI: 10.1016/J.Psep.2017.01.022 |
0.332 |
|
2015 |
Aichinger C, Mulzer J, Rinner U. Synthesis of the C6-C14 Fragment of Euphosalicin Synlett. 26: 1852-1856. DOI: 10.1055/S-0034-1380422 |
0.679 |
|
2015 |
Rinner U. Progress in the preparation of jatrophane diterpenes European Journal of Organic Chemistry. 2015: 3197-3219. DOI: 10.1002/Ejoc.201403598 |
0.397 |
|
2014 |
Fürst R, Lentsch C, Rinner U. Synthetic studies towards an advanced precursor of the jatrophane diterpene Pl-4 Synthesis (Germany). 46: 357-367. DOI: 10.1055/S-0033-1338565 |
0.783 |
|
2014 |
Siengalewicz P, Mulzer J, Rinner U. Synthesis of Esters and Lactones Comprehensive Organic Synthesis: Second Edition. 6: 355-410. DOI: 10.1016/B978-0-08-097742-3.00612-1 |
0.476 |
|
2014 |
Lentsch C, Fürst R, Mulzer J, Rinner U. Jatrophane diterpenes: Preparation of the western fragment of pl-3 European Journal of Organic Chemistry. 2014: 919-923. DOI: 10.1002/Ejoc.201301616 |
0.778 |
|
2013 |
Siengalewicz P, Mulzer J, Rinner U. Lycopodium alkaloids--synthetic highlights and recent developments. The Alkaloids. Chemistry and Biology. 72: 1-151. PMID 24712098 DOI: 10.1016/B978-0-12-407774-4.00001-7 |
0.624 |
|
2013 |
Di Giuro CML, Konstantinovics C, Rinner U, Nowikow C, Leitner E, Straganz GD. Chiral Hydroxylation at the Mononuclear Nonheme Fe(II) Center of 4-(S) Hydroxymandelate Synthase - A Structure-Activity Relationship Analysis Plos One. 8. PMID 23935907 DOI: 10.1371/Journal.Pone.0068932 |
0.402 |
|
2013 |
Fürst R, Rinner U. Synthesis of an advanced intermediate of the jatrophane diterpene Pl-4: A dibromide coupling approach Journal of Organic Chemistry. 78: 8748-8758. PMID 23895274 DOI: 10.1021/Jo401480T |
0.749 |
|
2013 |
Fürst R, Lentsch C, Rinner U. Towards the Total Synthesis of Pl-3: Preparation of the Eastern Fragment through a Diastereoselective SmI2-Mediated Reformatsky Reaction. European Journal of Organic Chemistry. 2013: 2293-2297. PMID 23687456 DOI: 10.1002/Ejoc.201300148 |
0.8 |
|
2013 |
Lentsch C, Fürst R, Rinner U. Enyne metathesis approach towards the cyclopentane motif of jatrophane diterpenes Synlett. 24: 2665-2670. DOI: 10.1055/S-0033-1339923 |
0.789 |
|
2013 |
Fürst R, Lentsch C, Rinner U. Towards the total synthesis of Pl-3: Preparation of the eastern fragment through a diastereoselective SmI2-mediated reformatsky reaction European Journal of Organic Chemistry. 2293-2297. DOI: 10.1002/ejoc.201300148 |
0.794 |
|
2012 |
Rinner U, Hudlicky T. Synthesis of morphine alkaloids and derivatives. Topics in Current Chemistry. 309: 33-66. PMID 21547687 DOI: 10.1007/128_2011_133 |
0.575 |
|
2012 |
Siengalewicz P, Mulzer J, Rinner U. 2.15 Selected Diastereoselective Reactions: Substrate Controlled Stereoselective Conjugate Addition Reactions with Organocopper Reagents Comprehensive Chirality. 2: 441-471. DOI: 10.1016/B978-0-08-095167-6.00225-1 |
0.342 |
|
2012 |
Rinner U. 2.9 Chiral Pool Synthesis: Chiral Pool Syntheses from cis-Cyclohexadiene Diols Comprehensive Chirality. 2: 240-267. DOI: 10.1016/B978-0-08-095167-6.00219-6 |
0.305 |
|
2011 |
Adams DR, Aichinger C, Rinner U, Hudlicky T. Chemoenzymatic synthesis of idesolide from benzoic acid Synlett. 725-729. DOI: 10.1055/S-0030-1259694 |
0.504 |
|
2011 |
Siengalewicz P, Mulzer J, Rinner U. Synthesis of protoilludanes and related sesquiterpenes European Journal of Organic Chemistry. 7041-7055. DOI: 10.1002/Ejoc.201101220 |
0.648 |
|
2010 |
Collins J, Rinner U, Moser M, Hudlicky T, Ghiviriga I, Romero AE, Kornienko A, Ma D, Griffin C, Pandey S. Chemoenzymatic synthesis of Amaryllidaceae constituents and biological evaluation of their C-1 analogues. The next generation synthesis of 7-deoxypancratistatin and trans-dihydrolycoricidine. The Journal of Organic Chemistry. 75: 3069-84. PMID 20373760 DOI: 10.1021/Jo1003136 |
0.607 |
|
2010 |
Rinner U, Lentsch C, Aichinger C. Syntheses of Galbulimima alkaloids Synthesis. 3763-3784. DOI: 10.1055/S-0030-1258251 |
0.777 |
|
2009 |
Fürst R, Zupkó I, Berényi A, Ecker GF, Rinner U. Synthesis and antitumor-evaluation of cyclopropyl-containing combretastatin analogs. Bioorganic & Medicinal Chemistry Letters. 19: 6948-51. PMID 19879758 DOI: 10.1016/J.Bmcl.2009.10.064 |
0.412 |
|
2009 |
Lentsch C, Rinner U. General synthesis of highly functionalized cyclopentane segments for the preparation of jatrophane diterpenes Organic Letters. 11: 5326-5328. PMID 19856927 DOI: 10.1021/Ol902221Y |
0.787 |
|
2009 |
Rinner U, Mulzer J. Elements of Synthesis Planning. By R. W. Hoffmann. Angewandte Chemie. 48: 9590-9591. DOI: 10.1002/Anie.200905457 |
0.525 |
|
2008 |
Siengalewicz P, Rinner U, Mulzer J. Recent progress in the total synthesis of naphthyridinomycin and lemonomycin tetrahydroisoquinoline antitumor antibiotics (TAAs). Chemical Society Reviews. 37: 2676-90. PMID 19020681 DOI: 10.1039/B804167A |
0.616 |
|
2008 |
Collins J, Drouin M, Sun X, Rinner U, Hudlicky T. Total synthesis of 7-deoxypancratistatin-1-carboxaldehyde and carboxylic acid via solvent-free intramolecular aziridine opening: phenanthrene to phenanthridone cyclization strategy. Organic Letters. 10: 361-4. PMID 18163635 DOI: 10.1021/Ol702440F |
0.58 |
|
2008 |
Rinner U, Mulzer J. The Way of Synthesis. Evolution of Design and Methods for Natural Products. Von Tomáš Hudlický und Josephine W. Reed. Angewandte Chemie. 120: 32-32. DOI: 10.1002/Ange.200785550 |
0.577 |
|
2006 |
Hudlicky T, Moser M, Banfield SC, Rinner U, Chapuis JC, Pettit GR. Cyclotrimerization approach to unnatural structural modifications of pancratistatin and other amaryllidaceae constituents - Synthesis and biological evaluation Canadian Journal of Chemistry. 84: 1313-1337. DOI: 10.1139/V06-078 |
0.586 |
|
2005 |
Hudlicky T, Rinner U, Finn KJ, Ghiviriga I. Reactions of indole derivatives with oxiranes and aziridines on silica. Synthesis of beta-carbolin-1-one mimic of pancratistatin. The Journal of Organic Chemistry. 70: 3490-9. PMID 15844982 DOI: 10.1021/Jo040292C |
0.781 |
|
2005 |
Rinner U, Hudlicky T. Synthesis of amaryllidaceae constituents - An update Synlett. 365-387. DOI: 10.1055/S-2005-862382 |
0.571 |
|
2005 |
Hudlicky T, Rinner U, Finn KJ, Ghiviriga I. Reactions of Indole Derivatives with Oxiranes and Aziridines on Silica. Synthesis of a β-Carbolin-1-one Mimic (XIII) of Pancratistatin. Cheminform. 36. DOI: 10.1002/chin.200538124 |
0.507 |
|
2004 |
Rinner U, Hudlicky T, Gordon H, Pettit GR. A beta-carboline-1-one mimic of the anticancer Amaryllidaceae constituent pancratistatin: synthesis and biological evaluation. Angewandte Chemie (International Ed. in English). 43: 5342-6. PMID 15468184 DOI: 10.1002/Anie.200460218 |
0.457 |
|
2004 |
Rinner U, Hillebrenner HL, Adams DR, Hudlicky T, Pettit GR. Synthesis and biological activity of some structural modifications of pancratistatin. Bioorganic & Medicinal Chemistry Letters. 14: 2911-5. PMID 15125958 DOI: 10.1016/J.Bmcl.2004.03.032 |
0.51 |
|
2003 |
Rinner U, Adams DR, Dos Santos ML, Abboud KA, Hudlicky T. New application of Burgess reagent in its reaction with epoxides Synlett. 1247-1252. DOI: 10.1055/S-2003-40356 |
0.562 |
|
2002 |
Hudlicky T, Rinner U, Gonzalez D, Akgun H, Schilling S, Siengalewicz P, Martinot TA, Pettit GR. Total synthesis and biological evaluation of Amaryllidaceae alkaloids: narciclasine, ent-7-deoxypancratistatin, regioisomer of 7-deoxypancratistatin, 10b-epi-deoxypancratistatin, and truncated derivatives. The Journal of Organic Chemistry. 67: 8726-43. PMID 12467383 DOI: 10.1021/Jo020129M |
0.782 |
|
2002 |
Rinner U, Siengalewicz P, Hudlicky T. Total synthesis of epi-7-deoxypancratistatin via aza-Payne rearrangement and intramolecular cyclization. Organic Letters. 4: 115-7. PMID 11772104 DOI: 10.1021/Ol0169877 |
0.597 |
|
2002 |
Rinner U, Siengalewicz P, Hudlicky T. Total synthesis of epi-7-deoxypancratistatin via aza-payne rearrangement and intramolecular cyclization Organic Letters. 4: 115-117. DOI: 10.1021/ol0169877 |
0.616 |
|
2001 |
Schilling S, Rinner U, Chan C, Ghiviriga I, Hudlicky T. Structure assignment of aminoconduritols by 15N NMR correlation spectroscopy; synthesis of a positional isomer of 7-deoxypancratistatin Canadian Journal of Chemistry. 79: 1659-1667. DOI: 10.1139/Cjc-79-11-1659 |
0.661 |
|
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