Year |
Citation |
Score |
2018 |
Süsse L, Vogler M, Mewald M, Kemper B, Irran E, Oestreich M. Enantioselective Nazarov Cyclizations Catalyzed by an Axial Chiral, C6F5-Substituted Boron Lewis Acid. Angewandte Chemie (International Ed. in English). PMID 29978948 DOI: 10.1002/Anie.201806011 |
0.715 |
|
2018 |
Süsse L, Vogler M, Mewald M, Kemper B, Irran E, Oestreich M. Enantioselektive Nazarov-Cyclisierungen, die von einer axial-chiralen, C6
F5
-substituierten Bor-Lewis-Säure katalysiert werden Angewandte Chemie. 130: 11612-11615. DOI: 10.1002/Ange.201806011 |
0.686 |
|
2015 |
White KL, Mewald M, Movassaghi M. Direct Observation of Intermediates Involved in the Interruption of the Bischler-Napieralski Reaction. The Journal of Organic Chemistry. 80: 7403-11. PMID 26166404 DOI: 10.1021/Acs.Joc.5B01023 |
0.605 |
|
2015 |
Mewald M, Medley JW, Movassaghi M. ChemInform Abstract: Concise and Enantioselective Total Synthesis of (-)-Mehranine, (-)-Methylenebismehranine, and Related Aspidosperma Alkaloids. Cheminform. 46: no-no. DOI: 10.1002/chin.201515281 |
0.564 |
|
2014 |
Mewald M, Medley JW, Movassaghi M. Concise and enantioselective total synthesis of (-)-mehranine, (-)-methylenebismehranine, and related Aspidosperma alkaloids Angewandte Chemie - International Edition. 53: 11634-11639. PMID 25196158 DOI: 10.1002/Anie.201405609 |
0.619 |
|
2014 |
Hermeke J, Mewald M, Irran E, Oestreich M. Chemoselective tin-boron exchange aided by the use of dummy ligands at the tin atom Organometallics. 33: 5097-5100. DOI: 10.1021/Om500851R |
0.721 |
|
2014 |
Mewald M, Medley JW, Movassaghi M. Enantioselektive Totalsynthese von (−)-Mehranin, (−)-Methylenbismehranin und verwandtenAspidosperma-Alkaloiden Angewandte Chemie. 126: 11818-11823. DOI: 10.1002/Ange.201405609 |
0.524 |
|
2013 |
Hermeke J, Mewald M, Oestreich M. Experimental analysis of the catalytic cycle of the borane-promoted imine reduction with hydrosilanes: spectroscopic detection of unexpected intermediates and a refined mechanism. Journal of the American Chemical Society. 135: 17537-46. PMID 24180217 DOI: 10.1021/Ja409344W |
0.737 |
|
2013 |
Oestreich M, Hartmann E, Mewald M. Activation of the Si-B interelement bond: mechanism, catalysis, and synthesis. Chemical Reviews. 113: 402-41. PMID 23163551 DOI: 10.1021/Cr3003517 |
0.672 |
|
2012 |
Mewald M, Oestreich M. Illuminating the mechanism of the borane-catalyzed hydrosilylation of imines with both an axially chiral borane and silane. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 14079-84. PMID 22996207 DOI: 10.1002/Chem.201202693 |
0.611 |
|
2012 |
Mewald M, Schiffner JA, Oestreich M. A new direction in C-H alkenylation: silanol as a helping hand. Angewandte Chemie (International Ed. in English). 51: 1763-5. PMID 22250066 DOI: 10.1002/Anie.201107859 |
0.708 |
|
2012 |
Mewald M, Schiffner JA, Oestreich M. Ein neuer Weg der C-H-Alkenylierung: Silanol als helfende Hand Angewandte Chemie. 124: 1797-1799. DOI: 10.1002/Ange.201107859 |
0.716 |
|
2011 |
Mewald M, Fröhlich R, Oestreich M. An axially chiral, electron-deficient borane: synthesis, coordination chemistry, Lewis acidity, and reactivity. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 9406-14. PMID 21732446 DOI: 10.1002/Chem.201100724 |
0.58 |
|
2010 |
Weickgenannt A, Mewald M, Oestreich M. Asymmetric Si-O coupling of alcohols. Organic & Biomolecular Chemistry. 8: 1497-504. PMID 20237658 DOI: 10.1039/B925722E |
0.754 |
|
2010 |
Weickgenannt A, Mewald M, Muesmann TW, Oestreich M. Catalytic asymmetric Si-O coupling of simple achiral silanes and chiral donor-functionalized alcohols. Angewandte Chemie (International Ed. in English). 49: 2223-6. PMID 19967693 DOI: 10.1002/Anie.200905561 |
0.755 |
|
2010 |
Mewald M, Weickgenannt A, Fröhlich R, Oestreich M. Expeditious synthesis of TADDOL-derived phosphoramidite and phosphonite ligands Tetrahedron Asymmetry. 21: 1232-1237. DOI: 10.1016/J.Tetasy.2010.03.010 |
0.738 |
|
2010 |
Weickgenannt A, Mewald M, Muesmann T, Oestreich M. Katalytische asymmetrische Si-O-Kupplung einfacher achiraler Silane und chiraler donorfunktionalisierter Alkohole Angewandte Chemie. 122: 2269-2272. DOI: 10.1002/Ange.200905561 |
0.746 |
|
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