Year |
Citation |
Score |
2024 |
Eggert A, Schuppe KT, Fuchs HLS, Brönstrup M, Kalesse M. Total Synthesis of Acanthodoral Using a Rearrangement Strategy. Organic Letters. PMID 38165657 DOI: 10.1021/acs.orglett.3c03717 |
0.32 |
|
2021 |
Lücke D, Kalesse M. Synthesis of Desepoxy-Tedanolide C. Chemistry (Weinheim An Der Bergstrasse, Germany). 27: 7085-7089. PMID 33769622 DOI: 10.1002/chem.202100553 |
0.326 |
|
2020 |
Eggert A, Etling C, Lübken D, Saxarra M, Kalesse M. Contiguous Quaternary Carbons: A Selection of Total Syntheses. Molecules (Basel, Switzerland). 25. PMID 32847075 DOI: 10.3390/Molecules25173841 |
0.373 |
|
2020 |
Geldsetzer J, Kalesse M. Towards the total synthesis of chondrochloren A: synthesis of the ()-enamide fragment. Beilstein Journal of Organic Chemistry. 16: 670-673. PMID 32362944 DOI: 10.3762/Bjoc.16.64 |
0.409 |
|
2020 |
Channar PA, Saeed A, Afzal S, Hussain D, Kalesse M, Shehzadi SA, Iqbal J. Hydrazine clubbed 1,3-thiazoles as potent urease inhibitors: design, synthesis and molecular docking studies. Molecular Diversity. PMID 32095975 DOI: 10.1007/S11030-020-10057-7 |
0.324 |
|
2020 |
Linne Y, Schönwald A, Weißbach S, Kalesse M. Desymmetrization of C -Symmetric Bis(Boronic Esters) by Zweifel Olefinations. Chemistry (Weinheim An Der Bergstrasse, Germany). 26: 7998-8002. PMID 32068298 DOI: 10.1002/Chem.202000599 |
0.421 |
|
2019 |
Cordes M, Kalesse M. Very Recent Advances in Vinylogous Mukaiyama Aldol Reactions and Their Applications to Synthesis. Molecules (Basel, Switzerland). 24. PMID 31443344 DOI: 10.3390/Molecules24173040 |
0.443 |
|
2019 |
Lübken D, Saxarra M, Kalesse M. Tris(acetylacetonato) Iron(III): Recent Developments and Synthetic Applications Synthesis. 51: 161-177. DOI: 10.1055/S-0037-1610393 |
0.327 |
|
2018 |
Hansen TV, Tungen JE, Gerstman L, De Matteis R, Colas RA, Vik A, Chiang N, Serhan CN, Kalesse M, Dalli J. Resolving Inflammation - Synthesis, Configurational Assignment and Biological Evaluations of RvD1n-3 DPA. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30511787 DOI: 10.1002/Chem.201806029 |
0.412 |
|
2018 |
Lücke D, Linne Y, Hempel K, Kalesse M. Total Synthesis of Pericoannosin A. Organic Letters. 20: 4475-4477. PMID 30003789 DOI: 10.1021/Acs.Orglett.8B01768 |
0.417 |
|
2018 |
Stempel E, Kaml RF, Budisa N, Kalesse M. Painting argyrins blue: Negishi cross-coupling for synthesis of deep-blue tryptophan analogue β-(1-azulenyl)-l alanine and its incorporation into argyrin C. Bioorganic & Medicinal Chemistry. 26: 5259-5269. PMID 29729984 DOI: 10.1016/J.Bmc.2018.03.037 |
0.346 |
|
2017 |
Surup F, Kuhnert E, Böhm A, Wiebach V, Solga D, Engler H, Pendzialek T, Berkessel A, Stadler M, Kalesse M. The rickiols, 20-, 22-, and 24-membered macrolides from the ascomycete Hypoxylon rickii. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29168908 DOI: 10.1002/Chem.201704928 |
0.322 |
|
2017 |
Kalesse M, Müller R, Witte SNR, Hug JJ, Géraldy M. Biosynthesis, and Total Synthesis of Pyrronazol B a Secondary Metabolite from Nannocystis pusilla. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28944573 DOI: 10.1002/Chem.201703782 |
0.331 |
|
2017 |
Poock C, Kalesse M. Total Synthesis of Nannocystin Ax. Organic Letters. 19: 4536-4539. PMID 28809579 DOI: 10.1021/Acs.Orglett.7B02112 |
0.436 |
|
2017 |
Werner B, Kalesse M. Pinacol Coupling Strategy for the Construction of the Bicyclo[6.4.1]tridecane Framework of Schiglautone A. Organic Letters. 19: 1524-1526. PMID 28300417 DOI: 10.1021/Acs.Orglett.7B00288 |
0.407 |
|
2017 |
Kalesse M, Li J, Xing J, Lücke D, Lübken D, Millbrodt L, Plentz R. The Structure Elucidation of Haprolid Synthesis. 50: 529-538. DOI: 10.1055/S-0036-1591836 |
0.408 |
|
2017 |
Witte SNR, Hug JJ, Géraldy MNE, Müller R, Kalesse M. Frontispiece: Biosynthesis and Total Synthesis of Pyrronazol B: a Secondary Metabolite from Nannocystis pusilla Chemistry: a European Journal. 23. DOI: 10.1002/Chem.201786364 |
0.352 |
|
2016 |
Kalesse M, Böhm A, Kipper A, Wandelt V. Synthesis of Antibiotics. Current Topics in Microbiology and Immunology. 398: 419-445. PMID 27704271 DOI: 10.1007/82_2016_502 |
0.379 |
|
2016 |
Steinmetz H, Li J, Fu C, Zaburannyi N, Kunze B, Harmrolfs K, Schmitt V, Herrmann J, Reichenbach H, Höfle G, Kalesse M, Müller R. Isolation, Structure Elucidation, and (Bio)Synthesis of Haprolid, a Cell-Type-Specific Myxobacterial Cytotoxin. Angewandte Chemie (International Ed. in English). PMID 27404448 DOI: 10.1002/Anie.201603288 |
0.372 |
|
2016 |
Gerstmann L, Kalesse M. Total Synthesis of Aetheramide A. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 11210-2. PMID 27303862 DOI: 10.1002/Chem.201602682 |
0.422 |
|
2016 |
Tautz T, Hoffmann J, Hoffmann T, Steinmetz H, Washausen P, Kunze B, Huch V, Kitsche A, Reichenbach H, Höfle G, Müller R, Kalesse M. Isolation, Structure Elucidation, Biosynthesis, and Synthesis of Antalid, a Secondary Metabolite from Polyangium species. Organic Letters. PMID 27220069 DOI: 10.1021/Acs.Orglett.6B00810 |
0.372 |
|
2016 |
Parthasarathy G, Eggert U, Kalesse M. Correction to Synthesis of Omphadiol and Pyxidatol C. Organic Letters. 18: 2792. PMID 27187085 DOI: 10.1021/Acs.Orglett.6B01361 |
0.371 |
|
2016 |
Parthasarathy G, Eggert U, Kalesse M. Synthesis of (+)-Omphadiol and (+)-Pyxidatol C. Organic Letters. 18: 2320-2. PMID 27105390 DOI: 10.1021/Acs.Orglett.6B00814 |
0.42 |
|
2015 |
Lu HH, Hinkelmann B, Tautz T, Li J, Sasse F, Franke R, Kalesse M. Paleo-soraphens: chemical total syntheses and biological studies. Organic & Biomolecular Chemistry. PMID 26119264 DOI: 10.1039/C5Ob01249J |
0.745 |
|
2015 |
Naini A, Muthukumar Y, Raja A, Franke R, Harrier I, Smith AB, Lee D, Taylor RE, Sasse F, Kalesse M. The synthesis and biological evaluation of desepoxyisotedanolide and a comparison with desepoxytedanolide. Angewandte Chemie (International Ed. in English). 54: 6935-9. PMID 25914374 DOI: 10.1002/Anie.201501526 |
0.341 |
|
2015 |
Kalesse M. Ekkehard Winterfeldt (1932-2014). Angewandte Chemie (International Ed. in English). 54: 35. PMID 25476468 DOI: 10.1002/Anie.201410838 |
0.332 |
|
2015 |
Bluhm N, Kalesse M. Synthesis of a C20-Deoxygenated Spirangien Derivative for Target Identification Synlett. 26: 797-801. DOI: 10.1055/S-0034-1379980 |
0.45 |
|
2015 |
Naini A, Fohrer J, Kalesse M. The Synthesis of Desepoxy-Isotedanolide - A Potential Biosynthetic Precursor of Tedanolide European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201500568 |
0.401 |
|
2015 |
Bruns N, Collisi W, Bernecker S, Stadler M, Richter C, Schwalbe H, Kalesse M. Spirangien Derivatives from the Myxobacterium Sorangium cellulosum: Isolation, Structure Elucidation, and Biological Activity European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201403353 |
0.33 |
|
2014 |
Hartmann O, Kalesse M. The structure elucidation and total synthesis of β-lipomycin. Angewandte Chemie (International Ed. in English). 53: 7335-8. PMID 24850084 DOI: 10.1002/Anie.201402259 |
0.403 |
|
2014 |
Kalesse M, Cordes M, Symkenberg G, Lu HH. The vinylogous Mukaiyama aldol reaction (VMAR) in natural product synthesis. Natural Product Reports. 31: 563-94. PMID 24595879 DOI: 10.1039/C3Np70102F |
0.776 |
|
2014 |
Symkenberg G, Kalesse M. Structure elucidation and total synthesis of kulkenon. Angewandte Chemie (International Ed. in English). 53: 1795-8. PMID 24420412 DOI: 10.1002/Anie.201309386 |
0.447 |
|
2014 |
Gieseler MT, Kalesse M. Synthesis of angiolam A. Organic Letters. 16: 548-51. PMID 24341445 DOI: 10.1021/Ol403423R |
0.448 |
|
2014 |
Carreira EM, Joliton A, Gieseler MT, Kalesse M. Total Synthesis of (–)-Angiolam A Synfacts. 10: 226-226. DOI: 10.1055/S-0033-1340712 |
0.402 |
|
2013 |
Lu HH, Raja A, Franke R, Landsberg D, Sasse F, Kalesse M. Synthesis and biological evaluation of paleo-soraphens. Angewandte Chemie (International Ed. in English). 52: 13549-52. PMID 24346938 DOI: 10.1002/Anie.201305331 |
0.755 |
|
2013 |
Rentsch A, Landsberg D, Brodmann T, Bülow L, Girbig AK, Kalesse M. Synthesis and pharmacology of proteasome inhibitors. Angewandte Chemie (International Ed. in English). 52: 5450-88. PMID 23526565 DOI: 10.1002/Anie.201207900 |
0.406 |
|
2013 |
Kalesse M, Landsberg D, Hartmann O, Eggert U. Diastereodivergent Vinylogous Mukaiyama Aldol Reaction Synlett. 24: 1105-1108. DOI: 10.1055/S-0033-1338933 |
0.417 |
|
2013 |
Lu H, Raja A, Franke R, Landsberg D, Sasse F, Kalesse M. Die Synthese und biologische Evaluierung von Paläo‐Soraphenen Angewandte Chemie. 125: 13791-13795. DOI: 10.1002/Ange.201305331 |
0.334 |
|
2012 |
Rentsch A, Kalesse M. The total synthesis of corallopyronin A and myxopyronin B. Angewandte Chemie (International Ed. in English). 51: 11381-4. PMID 23042599 DOI: 10.1002/Anie.201206560 |
0.4 |
|
2012 |
Hartmann O, Kalesse M. The total synthesis of (-)-aurafuron A. Organic Letters. 14: 3064-7. PMID 22632656 DOI: 10.1021/Ol3011387 |
0.451 |
|
2012 |
Jahns C, Hoffmann T, Müller S, Gerth K, Washausen P, Höfle G, Reichenbach H, Kalesse M, Müller R. Pellasoren: structure elucidation, biosynthesis, and total synthesis of a cytotoxic secondary metabolite from Sorangium cellulosum. Angewandte Chemie (International Ed. in English). 51: 5239-43. PMID 22488911 DOI: 10.1002/Anie.201200327 |
0.392 |
|
2012 |
Zander W, Irschik H, Augustiniak H, Herrmann M, Jansen R, Steinmetz H, Gerth K, Kessler W, Kalesse M, Höfle G, Müller R. Sulfangolids, macrolide sulfate esters from Sorangium cellulosum Chemistry - a European Journal. 18: 6264-6271. PMID 22488821 DOI: 10.1002/Chem.201100851 |
0.308 |
|
2012 |
Symkenberg G, Kalesse M. Syn-selective vinylogous Kobayashi aldol reaction. Organic Letters. 14: 1608-11. PMID 22400997 DOI: 10.1021/Ol300353W |
0.412 |
|
2012 |
Diaz N, Zhu M, Ehrlich G, Eggert U, Muthukumar Y, Sasse F, Kalesse M. An improved route to (+)-tedanolide and analysis of its subtle effects controlling conformation and biological behaviour. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 4946-52. PMID 22392854 DOI: 10.1002/Chem.201103038 |
0.433 |
|
2012 |
Diaz N, Naini A, Muthukumar Y, Sasse F, Kalesse M. Synthesis of Simplified Tedanolide Analogues-Connecting Tedanolide to Myriaporone and Gephyronic Acid Chemmedchem. 7: 771-775. PMID 22383258 DOI: 10.1002/Cmdc.201100576 |
0.341 |
|
2012 |
Kalesse M. Biomimetic Organic Synthesis. Edited by Erwan Poupon and Bastien Nay. Angewandte Chemie. 51: 583-583. DOI: 10.1002/Anie.201107291 |
0.341 |
|
2012 |
Kalesse M. Biomimetic Organic Synthesis. Herausgegeben von Erwan Poupon und Bastien Nay. Angewandte Chemie. 124: 603-603. DOI: 10.1002/Ange.201107291 |
0.345 |
|
2011 |
Bülow L, Naini A, Fohrer J, Kalesse M. A kiyooka aldol approach for the synthesis of the C(14)-C(23) segment of the diastereomeric analog of tedanolide C Organic Letters. 13: 6038-6041. PMID 22026452 DOI: 10.1021/Ol202515X |
0.354 |
|
2011 |
Gieseler MT, Kalesse M. Asymmetric vinylogous Mukaiyama aldol reaction of aldehyde-derived dienolates. Organic Letters. 13: 2430-2. PMID 21473644 DOI: 10.1021/Ol2006727 |
0.436 |
|
2010 |
Kena Diba A, Noll C, Richter M, Gieseler MT, Kalesse M. Intramolecular stereoselective protonation of aldehyde-derived enolates. Angewandte Chemie (International Ed. in English). 49: 8367-9. PMID 20878962 DOI: 10.1002/Anie.201004619 |
0.347 |
|
2010 |
Brodmann T, Janssen D, Kalesse M. Total synthesis of chivosazole F. Journal of the American Chemical Society. 132: 13610-1. PMID 20836495 DOI: 10.1021/Ja107290S |
0.383 |
|
2010 |
Bülow L, Nickeleit I, Girbig AK, Brodmann T, Rentsch A, Eggert U, Sasse F, Steinmetz H, Frank R, Carlomagno T, Malek NP, Kalesse M. Synthesis and biological characterization of argyrin F. Chemmedchem. 5: 832-6. PMID 20358576 DOI: 10.1002/Cmdc.201000080 |
0.315 |
|
2010 |
Schäckel R, Hinkelmann B, Sasse F, Kalesse M. The synthesis of novel disorazoles. Angewandte Chemie (International Ed. in English). 49: 1619-22. PMID 20099286 DOI: 10.1002/Anie.200906450 |
0.446 |
|
2010 |
Rand K, Noll C, Schiebel HM, Kemken D, Dülcks T, Kalesse M, Heinz DW, Layer G. The oxygen-independent coproporphyrinogen III oxidase HemN utilizes harderoporphyrinogen as a reaction intermediate during conversion of coproporphyrinogen III to protoporphyrinogen IX. Biological Chemistry. 391: 55-63. PMID 19919179 DOI: 10.1515/Bc.2010.006 |
0.35 |
|
2010 |
Landsberg D, Kalesse M. Synthesis of Symmetrical Ureasby (Diacetoxyiodo)benzene-Induced Hofmann Rearrangement Synlett. 2010: 1104-1106. DOI: 10.1055/S-0029-1219566 |
0.357 |
|
2010 |
Brodmann T, Janssen D, Sasse F, Irschik H, Jansen R, Müller R, Kalesse M. Isolation and synthesis of chivotriene, a chivosazole shunt product from Sorangium cellulosum European Journal of Organic Chemistry. 5155-5159. DOI: 10.1002/Ejoc.201000781 |
0.403 |
|
2010 |
Kalesse M, Quitschalle M, Khandavalli CP, Saeed A. ChemInform Abstract: Total Synthesis of (-)-Callystatin A. Cheminform. 33: no-no. DOI: 10.1002/chin.200205218 |
0.324 |
|
2009 |
Lorenz M, Bluhm N, Kalesse M. Studies on the C22-C23 Aldol Coupling of Spirangien Synthesis. 2009: 3061-3066. DOI: 10.1055/S-0029-1216918 |
0.445 |
|
2009 |
Brodmann T, Lorenz M, Schäckel R, Simsek S, Kalesse M. Highly Stereoselective AldolReactions in the Total Syntheses of Complex Natural Products Synlett. 2009: 174-192. DOI: 10.1055/S-0028-1087520 |
0.472 |
|
2009 |
Simsek S, Kalesse M. Enantioselective synthesis of polyketide segments through vinylogous Mukaiyama aldol reactions Tetrahedron Letters. 50: 3485-3488. DOI: 10.1016/J.Tetlet.2009.03.013 |
0.409 |
|
2008 |
Roy M, Kalesse M. Syntheses of the tedanolides. Natural Product Reports. 25: 862-70. PMID 18820755 DOI: 10.1039/B719607E |
0.347 |
|
2008 |
Lorenz M, Kalesse M. Synthesis of the C10-C32 core structure of spirangien A. Organic Letters. 10: 4371-4. PMID 18754592 DOI: 10.1021/Ol8018105 |
0.414 |
|
2008 |
Eggert U, Diestel R, Sasse F, Jansen R, Kunze B, Kalesse M. Chondramide C: synthesis, configurational assignment, and structure-activity relationship studies. Angewandte Chemie (International Ed. in English). 47: 6478-82. PMID 18624309 DOI: 10.1002/Anie.200801156 |
0.373 |
|
2008 |
Ehrlich G, Hassfeld J, Eggert U, Kalesse M. The total synthesis of (+)-tedanolide--A macrocyclic polyketide from marine sponge Tedania ignis Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 2232-2247. PMID 18165955 DOI: 10.1002/Chem.200701529 |
0.441 |
|
2008 |
Rahn N, Kalesse M. The total synthesis of chlorotonil A. Angewandte Chemie (International Ed. in English). 47: 597-9. PMID 18041801 DOI: 10.1002/Anie.200703930 |
0.444 |
|
2008 |
Rahn N, Kalesse M. Synthesis of Chlorotonil A Synfacts. 2008: 557-557. DOI: 10.1055/S-2008-1072600 |
0.449 |
|
2008 |
Schübel N, Roy M, Kalesse M. Syntheses of the tedanolides and myriaporones Comptes Rendus Chimie. 11: 1419-1446. DOI: 10.1016/J.Crci.2008.05.013 |
0.355 |
|
2007 |
Simsek S, Horzella M, Kalesse M. Oxazaborolidinone-promoted vinylogous Mukaiyama aldol reactions. Organic Letters. 9: 5637-9. PMID 18052187 DOI: 10.1021/Ol702640W |
0.341 |
|
2007 |
Janssen D, Kalesse M. Synthesis of the C15-C35 Segment of Chivosazole A Synlett. 2007: 2667-2670. DOI: 10.1055/S-2007-991049 |
0.328 |
|
2007 |
Lorenz M, Kalesse M. Synthesis of the C23–C32 fragment of spirangien Tetrahedron Letters. 48: 2905-2907. DOI: 10.1016/J.Tetlet.2007.02.081 |
0.443 |
|
2006 |
Ehrlich G, Hassfeld J, Eggert U, Kalesse M. The total synthesis of (+)-tedanolide. Journal of the American Chemical Society. 128: 14038-9. PMID 17061881 DOI: 10.1021/Ja0659572 |
0.444 |
|
2006 |
Stelmakh A, Stellfeld T, Kalesse M. Tandem intramolecular Michael-aldol reaction as a tool for the construction of the C-ring of hexacyclinic acid. Organic Letters. 8: 3485-8. PMID 16869641 DOI: 10.1021/Ol061096Q |
0.412 |
|
2006 |
Liesener FP, Jannsen U, Kalesse M. Synthesis of the Northern Hemisphere of Amphidinolide H2 Synthesis. 2006: 2590-2602. DOI: 10.1055/S-2006-942459 |
0.462 |
|
2005 |
Hassfeld J, Kalesse M, Stellfeld T, Christmann M. Asymmetric total synthesis of complex marine natural products. Advances in Biochemical Engineering/Biotechnology. 97: 133-203. PMID 16261808 DOI: 10.1007/B135825 |
0.657 |
|
2005 |
Liesener FP, Kalesse M. Synthesis of the C19-C26 Segment of Amphidinolide H2 Synlett. 2005: 2236-2238. DOI: 10.1055/S-2005-872236 |
0.365 |
|
2005 |
Hassfeld J, Eggert U, Kalesse M. Synthesis of the C1-C17 Macrolactone of Tedanolide Synthesis. 2005: 1183-1199. DOI: 10.1055/S-2005-865302 |
0.404 |
|
2005 |
Rahn N, Kalesse M. A one-pot non-aldol-aldol vinylogous Mukaiyama aldol tandem sequence for the rapid construction of polyketide frameworks Synlett. 2005: 863-865. DOI: 10.1055/S-2005-863743 |
0.422 |
|
2005 |
Ehrlich G, Kalesse M. Synthesis of the C13-C23 segment of tedanolide Synlett. 655-657. DOI: 10.1055/S-2005-862391 |
0.366 |
|
2005 |
Hassfeld J, Eggert U, Kalesse M. Synthesis of the C1—C17 Macrolactone of Tedanolide (I). Cheminform. 36. DOI: 10.1002/chin.200543223 |
0.343 |
|
2004 |
Stellfeld T, Bhatt U, Kalesse M. Synthesis of the A,B,C-ring system of hexacyclinic acid Organic Letters. 6: 3889-3892. PMID 15496056 DOI: 10.1021/Ol048720O |
0.413 |
|
2004 |
Kirschning A, Chen GW, Jaunzems J, Jesberger M, Kalesse M, Lindner M. Synthesis of extended spacer-linked neooligodeoxysaccharides by metathesis olefination and evaluation of their RNA-binding properties Tetrahedron. 60: 3505-3521. DOI: 10.1016/J.Tet.2004.02.013 |
0.36 |
|
2004 |
Kalesse M. Pflichtlektüre für Synthesechemiker: Classics in Total Synthesis II. Von K. C. Nicolaou, S. A. Snyder, Wiley-VCH, Weinheim 2003.639 Seiten, brosch. 69,-Euro. ISBN 3-527-30684-6 Nachrichten Aus Der Chemie. 52: 472-472. DOI: 10.1002/Nadc.20040520433 |
0.304 |
|
2003 |
Kalesse M, Chary KP, Quitschalle M, Burzlaff A, Kasper C, Scheper T. The total synthesis of (-)-callystatin A. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 1129-36. PMID 12596149 DOI: 10.1002/CHIN.200324200 |
0.508 |
|
2002 |
Hassfeld J, Kalesse M. Synthesis of the C1-C11 segment of tedanolide via vinylogous Mukaiyama aldol reaction Synlett. 2002: 2007-2010. DOI: 10.1055/S-2002-35582 |
0.474 |
|
2002 |
Kalesse M, Christmann M. The chemistry and biology of the leptomycin family Synthesis. 2002: 981-1003. DOI: 10.1055/S-2002-31946 |
0.592 |
|
2002 |
Hassfeld J, Kalesse M. Advances in the vinylogous Mukaiyama aldol reaction and its application to the synthesis of the C1-C7 subunit of oleandolide Tetrahedron Letters. 43: 5093-5095. DOI: 10.1016/S0040-4039(02)00993-0 |
0.422 |
|
2001 |
Kalesse M, Christmann M, Bhatt U, Quitschalle M, Claus E, Saeed A, Burzlaff A, Kasper C, Haustedt LO, Hofer E, Scheper T, Beil W. The chemistry and biology of ratjadone Chembiochem. 2: 709-714. PMID 11828509 DOI: 10.1002/1439-7633(20010903)2:9<709::Aid-Cbic709>3.0.Co;2-7 |
0.584 |
|
2001 |
Hassfeld J, Christmann M, Kalesse M. Rapid access to polyketide scaffolds via vinylogous Mukaiyama aldol reactions. Organic Letters. 3: 3561-3564. PMID 11678708 DOI: 10.1021/Ol016677O |
0.632 |
|
2001 |
Bhatt U, Christmann M, Quitschalle M, Claus E, Kalesse M. The first total synthesis of (+)-ratjadone Journal of Organic Chemistry. 66: 1885-1893. PMID 11262141 DOI: 10.1021/Jo005768G |
0.689 |
|
2001 |
Christmann M, Kalesse M. Vinylogous Mukaiyama aldol reactions with triarylboranes Tetrahedron Letters. 42: 1269-1271. DOI: 10.1016/S0040-4039(00)02254-1 |
0.617 |
|
2001 |
Quitschalle M, Christmann M, Bhatt U, Kalesse M. Synthesis of unsaturated lactone moieties by asymmetric hetero Diels-Alder reactions with binaphthol-titanium complexes Tetrahedron Letters. 42: 1263-1265. DOI: 10.1016/S0040-4039(00)02213-9 |
0.668 |
|
2000 |
Christmann M, Bhatt U, Quitschalle M, Claus E, Kalesse M. Total Synthesis of (+)-Ratjadone. Angewandte Chemie (International Ed. in English). 39: 4364-4366. PMID 29711926 DOI: 10.1002/1521-3773(20001201)39:23<4364::Aid-Anie4364>3.0.Co;2-G |
0.665 |
|
2000 |
Kalesse M. The chemistry and biology of discodermolide. Chembiochem. 1: 171-175. PMID 11828409 DOI: 10.1002/1439-7633(20001002)1:3<171::Aid-Cbic171>3.0.Co;2-D |
0.301 |
|
2000 |
Christmann M, Bhatt U, Quitschalle M, Claus E, Kalesse M. Totalsynthese von (+)-Ratjadon Angewandte Chemie. 112: 4535-4538. DOI: 10.1002/1521-3757(20001201)112:23<4535::Aid-Ange4535>3.0.Co;2-K |
0.53 |
|
1999 |
Quitschalle M, Kalesse M. Improved synthesis of the northern hemisphere of epothilone A by a Sharpless asymmetric dihydroxylation Tetrahedron Letters. 40: 7765-7768. DOI: 10.1016/S0040-4039(99)01659-7 |
0.44 |
|
1999 |
Christmann M, Kalesse M. The synthesis of the C15–C24 segment of Ratjadone Tetrahedron Letters. 40: 7201-7204. DOI: 10.1016/S0040-4039(99)01486-0 |
0.636 |
|
1999 |
Claus E, Kalesse M. Synthesis of the C6C16 polyene fragment of ratjadone, a potent cytotoxic metabolite from Sorangium cellulosum Tetrahedron Letters. 40: 4157-4160. DOI: 10.1016/S0040-4039(99)00716-9 |
0.351 |
|
1999 |
Gerlach K, Quitschalle M, Kalesse M. Synthesis of the northern hemisphere of epothiline a by a ten-membered ring closing metathesis reaction Tetrahedron Letters. 40: 3553-3556. DOI: 10.1016/S0040-4039(99)00550-X |
0.41 |
|
1999 |
Kalesse M, Quitschalle M, Claus E, Gerlach K, Pahl A, Meyer HH. The Formal Total Synthesis of Epothilone A European Journal of Organic Chemistry. 1999: 2817-2823. DOI: 10.1002/(Sici)1099-0690(199911)1999:11<2817::Aid-Ejoc2817>3.0.Co;2-L |
0.483 |
|
1998 |
Gerlach K, Quitschalle M, Kalesse M. Synthesis of the C7-C17 Segment of Epothilones by a 10-membered Ring Closing Metathesis Reaction Synlett. 1998: 1108-1110. DOI: 10.1055/S-1998-1870 |
0.378 |
|
1997 |
Oost T, Kalesse M. Synthesis of RNAse active site model systems using a steroid template Tetrahedron. 53: 8421-8438. DOI: 10.1016/S0040-4020(97)00526-7 |
0.355 |
|
1996 |
Kalesse M, Eh M. Enantioselective synthesis of the C1C9 segment of bryostatin by kinetic resolution of racemic β-keto esters Tetrahedron Letters. 37: 1767-1770. DOI: 10.1016/0040-4039(96)00172-4 |
0.382 |
|
1995 |
Eh M, Schomburg D, Schicht K, Kalesse M. An Efficient Synthesis Of Radicinin Analogues Tetrahedron. 51: 8983-8992. DOI: 10.1016/0040-4020(95)00491-P |
0.415 |
|
1991 |
Schinzer D, Kalesse M. Diastereoselective double michael additions of vinylogous esters and thexyldimethylsilyl triflate-induced cyclizations Tetrahedron Letters. 32: 4691-4694. DOI: 10.1016/S0040-4039(00)92283-4 |
0.357 |
|
1989 |
Schinzer D, Kalesse M. Silica Gel Catalyzed Cyclizations of Enones and Double Michael Additions of Vinylogous Amides: Efficient Synthesis of Bicyclo[2.2.2]octanones and Bicyclo-Hydrocarbazolones Synlett. 1989: 34-35. DOI: 10.1055/S-1989-34704 |
0.444 |
|
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