Year |
Citation |
Score |
2023 |
Dong W, Keess S, Molander GA. Nickel-Mediated Alkyl-, Acyl-, and Sulfonylcyanation of [1.1.1]Propellane. Chem Catalysis. 3. PMID 37840854 DOI: 10.1016/j.checat.2023.100608 |
0.369 |
|
2023 |
Levitre G, Keess S, Molander GA. Photoinduced Diastereoselective Aminoalkylation of Cubanes. Organic Letters. PMID 37216214 DOI: 10.1021/acs.orglett.3c01223 |
0.329 |
|
2023 |
Fernández DF, González-Esguevillas M, Keess S, Schäfer F, Mohr J, Shavnya A, Knauber T, Blakemore DC, MacMillan DWC. Redefining the Synthetic Logic of Medicinal Chemistry. Photoredox-Catalyzed Reactions as a General Tool for Aliphatic Core Functionalization. Organic Letters. PMID 37094230 DOI: 10.1021/acs.orglett.3c00994 |
0.62 |
|
2023 |
Huang W, Keess S, Molander GA. A General and Practical Route to Functionalized Bicyclo[1.1.1]Pentane-Heteroaryls Enabled by Photocatalytic Multicomponent Heteroarylation of [1.1.1]Propellane. Angewandte Chemie (International Ed. in English). e202302223. PMID 37059692 DOI: 10.1002/anie.202302223 |
0.355 |
|
2023 |
Huang W, Zheng Y, Keess S, Molander GA. A General and Modular Approach to BCP Alkylamines via Multicomponent Difunctionalization of [1.1.1]Propellane. Journal of the American Chemical Society. 145: 5363-5369. PMID 36802571 DOI: 10.1021/jacs.2c13298 |
0.301 |
|
2022 |
Zheng Y, Huang W, Dhungana RK, Granados A, Keess S, Makvandi M, Molander GA. Photochemical Intermolecular [3σ + 2σ]-Cycloaddition for the Construction of Aminobicyclo[3.1.1]heptanes. Journal of the American Chemical Society. 144: 23685-23690. PMID 36523116 DOI: 10.1021/jacs.2c11501 |
0.436 |
|
2022 |
Huang W, Keess S, Molander GA. One step synthesis of unsymmetrical 1,3-disubstituted BCP ketones nickel/photoredox-catalyzed [1.1.1]propellane multicomponent dicarbofunctionalization. Chemical Science. 13: 11936-11942. PMID 36320918 DOI: 10.1039/d2sc05100a |
0.363 |
|
2022 |
Huang W, Keess S, Molander GA. Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives. Journal of the American Chemical Society. PMID 35793500 DOI: 10.1021/jacs.2c05304 |
0.419 |
|
2021 |
Polites VC, Badir SO, Keess S, Jolit A, Molander GA. Nickel-Catalyzed Decarboxylative Cross-Coupling of Bicyclo[1.1.1]pentyl Radicals Enabled by Electron Donor-Acceptor Complex Photoactivation. Organic Letters. PMID 34100624 DOI: 10.1021/acs.orglett.1c01558 |
0.346 |
|
2021 |
Klare HFT, Albers L, Süsse L, Keess S, Müller T, Oestreich M. Silylium Ions: From Elusive Reactive Intermediates to Potent Catalysts. Chemical Reviews. PMID 33861564 DOI: 10.1021/acs.chemrev.0c00855 |
0.477 |
|
2017 |
Keess S, Oestreich M. Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes. Chemical Science. 8: 4688-4695. PMID 28936336 DOI: 10.1039/C7Sc01657C |
0.507 |
|
2017 |
Keess S, Oestreich M. Access to Fully Alkylated Germanes by B(C6F5)3-Catalyzed Transfer Hydrogermylation of Alkenes. Organic Letters. PMID 28358201 DOI: 10.1021/Acs.Orglett.7B00672 |
0.529 |
|
2016 |
Keess S, Oestreich M. 3-tert-Butyl-Substituted Cyclohexa-1,4-dienes as Isobutane Equivalents in the B(C6 F5 )3 -Catalyzed Transfer Hydro-tert-Butylation of Alkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27775187 DOI: 10.1002/Chem.201604397 |
0.579 |
|
2015 |
Keess S, Simonneau A, Oestreich M. Direct and transfer hydrosilylation reactions catalyzed by fully or partially fluorinated triarylboranes: A systematic study Organometallics. 34: 790-799. DOI: 10.1021/Om501284A |
0.663 |
|
2012 |
Enders D, Urbanietz G, Cassens-Sasse E, Keeß S, Raabe G. Control of six contiguous stereocenters in an asymmetric organocatalytic one-pot Michael/Michael/aldol addition sequence Advanced Synthesis and Catalysis. 354: 1481-1488. DOI: 10.1002/Adsc.201200120 |
0.303 |
|
Show low-probability matches. |