Tran M, Ready J
Angew Chem Int Ed Engl. 2024; 63(36):e202407824.
PMID: 38781007
PMC: 11347121.
DOI: 10.1002/anie.202407824.
Zhou J, Meng L, Yang Z, Wang J
Adv Sci (Weinh). 2024; 11(21):e2400096.
PMID: 38477439
PMC: 11151016.
DOI: 10.1002/advs.202400096.
Kastrati A, Jaquier V, Garbo M, Besnard C, Mazet C
ACS Org Inorg Au. 2023; 3(5):291-298.
PMID: 37810406
PMC: 10557126.
DOI: 10.1021/acsorginorgau.3c00024.
Gao S, Liu J, Troya D, Chen M
Angew Chem Int Ed Engl. 2023; 62(43):e202304796.
PMID: 37712934
PMC: 11144059.
DOI: 10.1002/anie.202304796.
Liu S, Liu Y, Flaget A, Zhang C, Mazet C
Org Lett. 2023; 25(37):6897-6901.
PMID: 37695719
PMC: 10521025.
DOI: 10.1021/acs.orglett.3c02627.
Asymmetric Syntheses of ()- or ()-β,γ-Unsaturated Ketones via Silane-Controlled Enantiodivergent Catalysis.
Liu J, Gao S, Miliordos E, Chen M
J Am Chem Soc. 2023; 145(36):19542-19553.
PMID: 37639380
PMC: 11144060.
DOI: 10.1021/jacs.3c02595.
Ligand Control in Co-Catalyzed Regio- and Enantioselective Hydroboration: Homoallyl Secondary Boronates via Uncommon 4,3-Hydroboration of 1,3-Dienes.
Parsutkar M, Bhunia S, Majumder M, Lalisse R, Hadad C, RajanBabu T
J Am Chem Soc. 2023; 145(13):7462-7481.
PMID: 36972549
PMC: 10563392.
DOI: 10.1021/jacs.3c00181.
Asymmetric synthesis of flavanols via Cu-catalyzed kinetic resolution of chromenes and their anti-inflammatory activity.
Yang Q, Wang Z, Hor C, Xiao H, Bian Z, Wang J
Sci Adv. 2022; 8(22):eabm9603.
PMID: 35658029
PMC: 9166297.
DOI: 10.1126/sciadv.abm9603.
Enantioselective Cu(I)-catalyzed borylative cyclization of enone-tethered cyclohexadienones and mechanistic insights.
Jadhav S, Dash S, Maurya S, Nanubolu J, Vanka K, Chegondi R
Nat Commun. 2022; 13(1):854.
PMID: 35165287
PMC: 8844005.
DOI: 10.1038/s41467-022-28288-7.
NHC-Ni catalyzed enantioselective synthesis of 1,4-dienes by cross-hydroalkenylation of cyclic 1,3-dienes and heterosubstituted terminal olefins.
Chen Y, Dang L, Ho C
Nat Commun. 2020; 11(1):2269.
PMID: 32385240
PMC: 7210895.
DOI: 10.1038/s41467-020-16139-2.
α-Silicon effect assisted Curtin-Hammett allylation using allylcopper reagents derived from 1,3-dienylsilanes.
Gao S, Chen M
Chem Sci. 2019; 10(32):7554-7560.
PMID: 31489170
PMC: 6713862.
DOI: 10.1039/c9sc02905b.
Facile access to functionalized chiral secondary benzylic boronic esters catalytic asymmetric hydroboration.
Chakrabarty S, Palencia H, Morton M, Carr R, Takacs J
Chem Sci. 2019; 10(18):4854-4861.
PMID: 31183035
PMC: 6520923.
DOI: 10.1039/c8sc05613g.
Cationic Co(I)-Intermediates for Hydrofunctionalization Reactions: Regio- and Enantioselective Cobalt-Catalyzed 1,2-Hydroboration of 1,3-Dienes.
Duvvuri K, Dewese K, Parsutkar M, Jing S, Mehta M, Gallucci J
J Am Chem Soc. 2019; 141(18):7365-7375.
PMID: 31020835
PMC: 6528837.
DOI: 10.1021/jacs.8b13812.
Racemic Vinylallenes in Catalytic Enantioselective Multicomponent Processes: Rapid Generation of Complexity through 1,6-Conjugate Additions.
Huang Y, Torker S, Li X, Del Pozo J, Hoveyda A
Angew Chem Int Ed Engl. 2019; 58(9):2685-2691.
PMID: 30653802
PMC: 6481603.
DOI: 10.1002/anie.201812535.
Copper-catalyzed enantioselective 1,2-borylation of 1,3-dienes.
Liu Y, Fiorito D, Mazet C
Chem Sci. 2018; 9(23):5284-5288.
PMID: 29997884
PMC: 6001400.
DOI: 10.1039/c8sc01538d.
Copper-Catalyzed Heteroarylboration of 1,3-Dienes with 3-Bromopyridines: A cine Substitution.
Smith K, Huang Y, Brown M
Angew Chem Int Ed Engl. 2018; 57(21):6146-6149.
PMID: 29697174
PMC: 6132256.
DOI: 10.1002/anie.201801139.
Enantioselective Synthesis of Trisubstituted Allenyl-B(pin) Compounds by Phosphine-Cu-Catalyzed 1,3-Enyne Hydroboration. Insights Regarding Stereochemical Integrity of Cu-Allenyl Intermediates.
Huang Y, Del Pozo J, Torker S, Hoveyda A
J Am Chem Soc. 2018; 140(7):2643-2655.
PMID: 29417810
PMC: 6019291.
DOI: 10.1021/jacs.7b13296.
Mechanism of the Ullmann Biaryl Ether Synthesis Catalyzed by Complexes of Anionic Ligands: Evidence for the Reaction of Iodoarenes with Ligated Anionic Cu Intermediates.
Giri R, Brusoe A, Troshin K, Wang J, Font M, Hartwig J
J Am Chem Soc. 2017; 140(2):793-806.
PMID: 29224350
PMC: 5810543.
DOI: 10.1021/jacs.7b11853.
Kinetic resolution of racemic 2-substituted 1,2-dihydroquinolines asymmetric Cu-catalyzed borylation.
Kong D, Han S, Wang R, Li M, Zi G, Hou G
Chem Sci. 2017; 8(6):4558-4564.
PMID: 28936333
PMC: 5590099.
DOI: 10.1039/c7sc01556a.
Enantioselective γ-borylation of unsaturated amides and stereoretentive Suzuki-Miyaura cross-coupling.
Hoang G, Takacs J
Chem Sci. 2017; 8(6):4511-4516.
PMID: 28758006
PMC: 5514528.
DOI: 10.1039/c7sc01093a.