Patil M, Ghosh K, RajanBabu T
J Am Chem Soc. 2024; 146(10):6604-6617.
PMID: 38431968
PMC: 11407689.
DOI: 10.1021/jacs.3c12020.
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.
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.
Connon R, Roche B, Rokade B, Guiry P
Chem Rev. 2021; 121(11):6373-6521.
PMID: 34019404
PMC: 8277118.
DOI: 10.1021/acs.chemrev.0c00844.
Hoveyda A, Zhou Y, Shi Y, Brown M, Wu H, Torker S
Angew Chem Int Ed Engl. 2020; 59(48):21304-21359.
PMID: 32364640
PMC: 7609658.
DOI: 10.1002/anie.202003755.
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.
Phosphonate-Directed Catalytic Asymmetric Hydroboration: Delivery of Boron to the More Substituted Carbon, Leading to Chiral Tertiary Benzylic Boronic Esters.
Chakrabarty S, Takacs J
ACS Catal. 2019; 8(11):10530-10536.
PMID: 31134137
PMC: 6533611.
DOI: 10.1021/acscatal.8b03591.
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.
Earth-Abundant Transition Metal Catalysts for Alkene Hydrosilylation and Hydroboration: Opportunities and Assessments.
Obligacion J, Chirik P
Nat Rev Chem. 2019; 2(5):15-34.
PMID: 30740530
PMC: 6365001.
DOI: 10.1038/s41570-018-0001-2.
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-based enhancement of scope and enantioselectivity for reactions involving a copper-substituted stereogenic carbon centre.
Lee J, Radomkit S, Torker S, Del Pozo J, Hoveyda A
Nat Chem. 2017; 10(1):99-108.
PMID: 29256506
PMC: 5753601.
DOI: 10.1038/nchem.2861.
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.
Synthesis of Chiral Tertiary Boronic Esters: Phosphonate-Directed Catalytic Asymmetric Hydroboration of Trisubstituted Alkenes.
Chakrabarty S, Takacs J
J Am Chem Soc. 2017; 139(17):6066-6069.
PMID: 28414243
PMC: 5423446.
DOI: 10.1021/jacs.7b02324.
γ-Selective directed catalytic asymmetric hydroboration of 1,1-disubstituted alkenes.
Smith S, Hoang G, Pal R, Bani Khaled M, Pelter L, Zeng X
Chem Commun (Camb). 2012; 48(100):12180-2.
PMID: 23145431
PMC: 3601746.
DOI: 10.1039/c2cc36199j.