Zhang J, Yang P, Shu W
Chem Sci. 2022; 13(38):11405-11410.
PMID: 36320572
PMC: 9533468.
DOI: 10.1039/d2sc04350e.
Calo F, Zimmer A, Bistoni G, Furstner A
J Am Chem Soc. 2022; 144(16):7465-7478.
PMID: 35420801
PMC: 9052758.
DOI: 10.1021/jacs.2c02258.
Tercenio Q, Alexanian E
Org Lett. 2021; 23(18):7215-7219.
PMID: 34463502
PMC: 8734645.
DOI: 10.1021/acs.orglett.1c02616.
Ma X, Murray B, Biscoe M
Nat Rev Chem. 2021; 4(11):584-599.
PMID: 33869786
PMC: 8049355.
DOI: 10.1038/s41570-020-00222-9.
Metrano A, Chinn A, Shugrue C, Stone E, Kim B, Miller S
Chem Rev. 2020; 120(20):11479-11615.
PMID: 32969640
PMC: 8006536.
DOI: 10.1021/acs.chemrev.0c00523.
A General Approach to Stereospecific Cross-Coupling Reactions of Nitrogen-Containing Stereocenters.
Ma X, Zhao H, Binayeva M, Ralph G, Diane M, Zhao S
Chem. 2020; 6(3):781-791.
PMID: 32440572
PMC: 7241476.
DOI: 10.1016/j.chempr.2020.02.002.
A Heteroleptic Dirhodium Catalyst for Asymmetric Cyclopropanation with α-Stannyl α-Diazoacetate. "Stereoretentive" Stille Coupling with Formation of Chiral Quarternary Carbon Centers.
Calo F, Furstner A
Angew Chem Int Ed Engl. 2020; 59(33):13900-13907.
PMID: 32426901
PMC: 7496581.
DOI: 10.1002/anie.202004377.
Photochemical Asymmetric Nickel-Catalyzed Acyl Cross-Coupling.
Gandolfo E, Tang X, Raha Roy S, Melchiorre P
Angew Chem Int Ed Engl. 2019; 58(47):16854-16858.
PMID: 31532568
PMC: 6900114.
DOI: 10.1002/anie.201910168.
Cross-Coupling of Heteroatomic Electrophiles.
Korch K, Watson D
Chem Rev. 2019; 119(13):8192-8228.
PMID: 31184483
PMC: 6620169.
DOI: 10.1021/acs.chemrev.8b00628.
Ni-Catalyzed Arylboration of Unactivated Alkenes: Scope and Mechanistic Studies.
Sardini S, Lambright A, Trammel G, Omer H, Liu P, Brown M
J Am Chem Soc. 2019; 141(23):9391-9400.
PMID: 31184148
PMC: 6688169.
DOI: 10.1021/jacs.9b03991.
Catalyst-Controlled 1,2- and 1,1-Arylboration of α-Alkyl Alkenyl Arenes.
Bergmann A, Dorn S, Smith K, Logan K, Brown M
Angew Chem Int Ed Engl. 2018; 58(6):1719-1723.
PMID: 30521697
PMC: 6823597.
DOI: 10.1002/anie.201812533.
Asymmetric synthesis via stereospecific C-N and C-O bond activation of alkyl amine and alcohol derivatives.
Pound S, Watson M
Chem Commun (Camb). 2018; 54(87):12286-12301.
PMID: 30283929
PMC: 6261259.
DOI: 10.1039/c8cc07093h.
Cu-catalyzed enantioselective synthesis of tertiary benzylic copper complexes and their addition to carbonyl compounds.
Cheng F, Lu W, Huang W, Wen L, Li M, Meng F
Chem Sci. 2018; 9(22):4992-4998.
PMID: 29938027
PMC: 5989696.
DOI: 10.1039/c8sc00827b.
Enantio- and Diastereoselective Synthesis of Hydroxy Bis(boronates) via Cu-Catalyzed Tandem Borylation/1,2-Addition.
Green J, Joannou M, Murray S, Zanghi J, Meek S
ACS Catal. 2018; 7(7):4441-4445.
PMID: 29520326
PMC: 5837064.
DOI: 10.1021/acscatal.7b01123.
Keeping Track of the Electrons.
Lucas E, Jarvo E
Acc Chem Res. 2018; 51(2):567-572.
PMID: 29364644
PMC: 6363120.
DOI: 10.1021/acs.accounts.7b00432.
Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes.
Logan K, Sardini S, White S, Brown M
J Am Chem Soc. 2017; 140(1):159-162.
PMID: 29271650
PMC: 5778876.
DOI: 10.1021/jacs.7b12160.
Stereospecific Electrophilic Fluorination of Alkylcarbastannatrane Reagents.
Ma X, Diane M, Ralph G, Chen C, Biscoe M
Angew Chem Int Ed Engl. 2017; 56(41):12663-12667.
PMID: 28833888
PMC: 8054978.
DOI: 10.1002/anie.201704672.
Cobalt-Catalyzed Carbonylative Cross-Coupling of Alkyl Tosylates and Dienes: Stereospecific Synthesis of Dienones at Low Pressure.
Sargent B, Alexanian E
J Am Chem Soc. 2017; 139(36):12438-12440.
PMID: 28829914
PMC: 5623099.
DOI: 10.1021/jacs.7b07983.
Enantioselective assembly of tertiary stereocenters multicomponent chemoselective cross-coupling of geminal chloro(iodo)alkanes.
Jiang X, Kulbitski K, Nisnevich G, Gandelman M
Chem Sci. 2017; 7(4):2762-2767.
PMID: 28660053
PMC: 5477020.
DOI: 10.1039/c5sc04378f.
Nickel-Catalyzed Enantioselective Cross-Coupling of N-Hydroxyphthalimide Esters with Vinyl Bromides.
Suzuki N, Hofstra J, Poremba K, Reisman S
Org Lett. 2017; 19(8):2150-2153.
PMID: 28375631
PMC: 5868419.
DOI: 10.1021/acs.orglett.7b00793.