| Year |
Citation |
Score |
| 2017 |
Poonpatana P, Gomes G, Hurrle T, Chardon K, Bräse S, Alabugin I, Masters KS. Formaldehyde-Extruding Homolytic Aromatic Substitution via C→O Transposition: Selective 'Traceless-Linker' access to Congested Biaryl Bonds. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28399331 DOI: 10.1002/Chem.201700085 |
0.453 |
|
| 2015 |
Wezeman T, Bräse S, Masters KS. Xanthone dimers: a compound family which is both common and privileged. Natural Product Reports. 32: 6-28. PMID 25226564 DOI: 10.1039/C4Np00050A |
0.431 |
|
| 2015 |
Wezeman T, Hu Y, McMurtrie J, Bräse S, Masters KS. Synthesis of Non-Symmetrical and Atropisomeric Dibenzo[1,3]diazepines: Pd/CPhos-Catalysed Direct Arylation of Bis-Aryl Aminals Australian Journal of Chemistry. 68: 1859-1865. DOI: 10.1071/Ch15465 |
0.505 |
|
| 2015 |
Masters KS. Multi-bond forming and iodo-selective base-promoted homolytic aromatic substitution Rsc Advances. 5: 29975-29986. DOI: 10.1039/C5Ra03460D |
0.371 |
|
| 2015 |
Lindner S, Bräse S, Masters KS. Simple and expedient metal-free C-H-functionalization of fluoro-arenes by the BHAS method - Scope and limitations Journal of Fluorine Chemistry. 179: 102-105. DOI: 10.1016/J.Jfluchem.2015.06.010 |
0.511 |
|
| 2014 |
Wezeman T, Masters KS, Bräse S. Double trouble--the art of synthesis of chiral dimeric natural products. Angewandte Chemie (International Ed. in English). 53: 4524-6. PMID 24700517 DOI: 10.1002/Anie.201402384 |
0.492 |
|
| 2014 |
Wezeman T, Masters K, Bräse S. Doppelt genäht hält besser - die Kunst der Synthese chiraler dimerer Naturstoffe Angewandte Chemie. 126: 4612-4614. DOI: 10.1002/Ange.201402384 |
0.443 |
|
| 2013 |
Masters KS, Bihlmeier A, Klopper W, Bräse S. Tethering for selective synthesis of 2,2'-biphenols: the acetal method. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 17827-35. PMID 24265263 DOI: 10.1002/Chem.201301969 |
0.531 |
|
| 2013 |
Bräse S, Gläser F, Kramer CS, Lindner S, Linsenmeier AM, Masters KS, Meister AC, Ruff BM, Zhong S. Progress in the chemistry of organic natural products. The chemistry of mycotoxins. Progress in the Chemistry of Organic Natural Products. 97: v-xv, 1-300. PMID 23781707 |
0.341 |
|
| 2013 |
Halbedl S, Kratzer MC, Rahm K, Crosta N, Masters KS, Zippert J, Bräse S, Gradl D. Synthesis of novel inhibitors blocking Wnt signaling downstream of β-catenin. Febs Letters. 587: 522-7. PMID 23357029 DOI: 10.1016/J.Febslet.2013.01.034 |
0.457 |
|
| 2013 |
Masters KS, Bräse S. The acetal concept: regioselective access to ortho,ortho-diphenols via dibenzo-1,3-dioxepines. Angewandte Chemie (International Ed. in English). 52: 866-9. PMID 23180634 DOI: 10.1002/Anie.201207485 |
0.544 |
|
| 2013 |
Crosta N, Müller S, Gradl D, Masters KS, Bräse S. Rediscovering the double friedel-crafts acylation: An expedient entry to phenanthrene-9,10-diones Synlett. 24: 951-954. DOI: 10.1055/S-0032-1318481 |
0.483 |
|
| 2012 |
Masters KS, Bräse S. Xanthones from fungi, lichens, and bacteria: the natural products and their synthesis. Chemical Reviews. 112: 3717-76. PMID 22617028 DOI: 10.1021/Cr100446H |
0.511 |
|
| 2012 |
Masters K, Bräse S. Das Acetal-Konzept: regioselektiver Zugang zuortho,ortho-Diphenolen über Dibenzo-1,3-dioxepine Angewandte Chemie. 125: 899-903. DOI: 10.1002/Ange.201207485 |
0.374 |
|
| 2011 |
Masters KS, Wallesch M, Bräse S. ortho-Bromo(propa-1,2-dien-1-yl)arenes: substrates for domino reactions. The Journal of Organic Chemistry. 76: 9060-7. PMID 21958309 DOI: 10.1021/Jo201679S |
0.468 |
|
| 2011 |
Masters KS, Rauws TR, Yadav AK, Herrebout WA, Van der Veken B, Maes BU. On the importance of an acid additive in the synthesis of pyrido[1,2-a]benzimidazoles by direct copper-catalyzed amination. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 6315-20. PMID 21509841 DOI: 10.1002/Chem.201100574 |
0.414 |
|
| 2011 |
Masters KS, Nieger M, Bräse S. Solid-state structure of some substituted hexahydro-1,4:5,8-diepoxy- naphthalenes Synlett. 399-401. DOI: 10.1055/S-0030-1259327 |
0.467 |
|
| 2010 |
Masters KS, Flynn BL. An efficient synthesis of (+/-)-frondosin B using a Stille-Heck reaction sequence. Organic & Biomolecular Chemistry. 8: 1290-2. PMID 20204197 DOI: 10.1039/B924542A |
0.342 |
|
| 2009 |
Masters KS, Flynn BL. Alternation of chemoselective control in Stille-Heck and Heck-Stille reaction sequences Advanced Synthesis and Catalysis. 351: 530-536. DOI: 10.1002/Adsc.200990014 |
0.339 |
|
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