Chennamsetti H, Rathore K, Chatterjee S, Kumar Mandal P, Katukojvala S
JACS Au. 2024; 4(6):2099-2107.
PMID: 38938806
PMC: 11200238.
DOI: 10.1021/jacsau.4c00134.
Mori N, Tachibana T, Umekubo N, Hayashi Y
Chem Sci. 2024; 15(15):5627-5632.
PMID: 38638214
PMC: 11023028.
DOI: 10.1039/d4sc00193a.
Hensinger M, Eitzinger A, Trapp O, Ofial A
Chemistry. 2023; 30(2):e202302764.
PMID: 37850416
PMC: 10962604.
DOI: 10.1002/chem.202302764.
Hensinger M, Closs A, Trapp O, Ofial A
Chem Commun (Camb). 2023; 59(52):8091-8094.
PMID: 37293771
PMC: 10297834.
DOI: 10.1039/d3cc01912h.
Yang G, Sun S, Li Z, Liu Y, Wang J
Commun Chem. 2023; 4(1):144.
PMID: 36697620
PMC: 9814953.
DOI: 10.1038/s42004-021-00580-5.
Asymmetric Organocatalysis: A Survival Guide to Medicinal Chemists.
Reyes E, Prieto L, Milelli A
Molecules. 2023; 28(1).
PMID: 36615465
PMC: 9822454.
DOI: 10.3390/molecules28010271.
Asymmetric Michael Addition in Synthesis of β-Substituted GABA Derivatives.
Han J, Escorihuela J, Fustero S, Landa A, Soloshonok V, Sorochinsky A
Molecules. 2022; 27(12).
PMID: 35744921
PMC: 9231165.
DOI: 10.3390/molecules27123797.
Kinetic Rationalization of Nonlinear Effects in Asymmetric Catalytic Cascade Reactions under Curtin-Hammett Conditions.
Ali C, Blackmond D, Bures J
ACS Catal. 2022; 12(10):5776-5785.
PMID: 35633899
PMC: 9127809.
DOI: 10.1021/acscatal.2c00783.
Organocatalytic Enantioselective α-Bromination of Aldehydes with -Bromosuccinimide.
Hutchinson G, Alamillo-Ferrer C, Fernandez-Pascual M, Bures J
J Org Chem. 2022; 87(12):7968-7974.
PMID: 35617931
PMC: 9207931.
DOI: 10.1021/acs.joc.2c00600.
Dynamic Stereochemistry of a Biphenyl-Bisprolineamide Model Catalyst and its Imidazolidinone Intermediates.
Golub T, Fessner M, Engelage E, Merten C
Chemistry. 2022; 28(45):e202201317.
PMID: 35611719
PMC: 9545261.
DOI: 10.1002/chem.202201317.
Monitoring Reaction Intermediates to Predict Enantioselectivity Using Mass Spectrometry.
Hilgers R, Teng S, Bris A, Pereverzev A, White P, Jansen J
Angew Chem Int Ed Engl. 2022; 61(36):e202205720.
PMID: 35561144
PMC: 9544535.
DOI: 10.1002/anie.202205720.
Unlocking New Reactivities in Enzymes by Iminium Catalysis.
Xu G, Poelarends G
Angew Chem Int Ed Engl. 2022; 61(30):e202203613.
PMID: 35524737
PMC: 9400869.
DOI: 10.1002/anie.202203613.
Recent progress in asymmetric synergistic catalysis - the judicious combination of selected chiral aminocatalysts with achiral metal catalysts.
Nielsen C, Linfoot J, Williams A, Spivey A
Org Biomol Chem. 2022; 20(14):2764-2778.
PMID: 35298581
PMC: 9082520.
DOI: 10.1039/d2ob00025c.
Continuous flow asymmetric synthesis of chiral active pharmaceutical ingredients and their advanced intermediates.
Otvos S, Kappe C
Green Chem. 2021; 23(17):6117-6138.
PMID: 34671222
PMC: 8447942.
DOI: 10.1039/d1gc01615f.
Asymmetric pyrone Diels-Alder reactions enabled by dienamine catalysis.
Cole C, Fuentes L, Snyder S
Chem Sci. 2021; 11(8):2175-2180.
PMID: 34123308
PMC: 8150114.
DOI: 10.1039/c9sc05738b.
Evidence for an enolate mechanism in the asymmetric Michael reaction of α,β-unsaturated aldehydes and ketones a hybrid system of two secondary amine catalysts.
Umekubo N, Terunuma T, Kwon E, Hayashi Y
Chem Sci. 2021; 11(41):11293-11297.
PMID: 34094371
PMC: 8162273.
DOI: 10.1039/d0sc03359f.
Green Chemistry Meets Asymmetric Organocatalysis: A Critical Overview on Catalysts Synthesis.
Antenucci A, Dughera S, Renzi P
ChemSusChem. 2021; 14(14):2785-2853.
PMID: 33984187
PMC: 8362219.
DOI: 10.1002/cssc.202100573.
Mechanistically Guided Design of an Efficient and Enantioselective Aminocatalytic α-Chlorination of Aldehydes.
Hutchinson G, Alamillo-Ferrer C, Bures J
J Am Chem Soc. 2021; 143(18):6805-6809.
PMID: 33929823
PMC: 8297727.
DOI: 10.1021/jacs.1c02997.
Telescoped Continuous Flow Synthesis of Optically Active γ-Nitrobutyric Acids as Key Intermediates of Baclofen, Phenibut, and Fluorophenibut.
Otvos S, Llanes P, Pericas M, Kappe C
Org Lett. 2020; 22(20):8122-8126.
PMID: 33026815
PMC: 7573919.
DOI: 10.1021/acs.orglett.0c03100.
The Cyclohexa-2,5-dienyl Group as a Placeholder for Hydrogen: Organocatalytic Michael Addition of an Acetaldehyde Surrogate.
Chen W, Fang H, Xie K, Oestreich M
Chemistry. 2020; 26(66):15126-15129.
PMID: 32808731
PMC: 7756304.
DOI: 10.1002/chem.202003764.