Im J, Choi J, Chung W
Commun Chem. 2024; 7(1):277.
PMID: 39592813
PMC: 11599576.
DOI: 10.1038/s42004-024-01365-2.
Moon H, Jung J, Choi J, Chung W
Nat Commun. 2024; 15(1):3710.
PMID: 38697968
PMC: 11066093.
DOI: 10.1038/s41467-024-47942-w.
Lubaev A, Rathnayake M, Eze F, Bayeh-Romero L
J Am Chem Soc. 2022; 144(29):13294-13301.
PMID: 35820071
PMC: 9945878.
DOI: 10.1021/jacs.2c04588.
Li J, Shi Y
RSC Adv. 2022; 11(22):13040-13046.
PMID: 35423889
PMC: 8697332.
DOI: 10.1039/d1ra02297k.
Steigerwald D, Soltanzadeh B, Sarkar A, Morgenstern C, Staples R, Borhan B
Chem Sci. 2021; 12(5):1834-1842.
PMID: 34163947
PMC: 8179065.
DOI: 10.1039/d0sc05224h.
A Convenient C-H Functionalization Platform for Pyrroloiminoquinone Alkaloid Synthesis.
Smith M, Falk I, Ikemoto H, Burns N
Tetrahedron. 2020; 75(24):3366-3370.
PMID: 31889735
PMC: 6937132.
DOI: 10.1016/j.tet.2019.05.009.
Merging Regiodivergent Catalysis with Atom-Economical Radical Arylation.
Muhlhaus F, Weissbarth H, Dahmen T, Schnakenburg G, Gansauer A
Angew Chem Int Ed Engl. 2019; 58(40):14208-14212.
PMID: 31394024
PMC: 6852184.
DOI: 10.1002/anie.201908860.
Asymmetric Alkene and Arene Halofunctionalization Reactions in Meroterpenoid Biosynthesis.
Moore B
Synlett. 2019; 29(4):401-409.
PMID: 31031546
PMC: 6483395.
DOI: 10.1055/s-0036-1590919.
Catalytic Regio- and Enantioselective Haloazidation of Allylic Alcohols.
Seidl F, Min C, Lopez J, Burns N
J Am Chem Soc. 2018; 140(46):15646-15650.
PMID: 30403852
PMC: 6499076.
DOI: 10.1021/jacs.8b10799.
Catalytic Enantioselective Dihalogenation in Total Synthesis.
Landry M, Burns N
Acc Chem Res. 2018; 51(5):1260-1271.
PMID: 29664281
PMC: 5987034.
DOI: 10.1021/acs.accounts.8b00064.
Asymmetric Synthesis of Gonytolide A: Strategic Use of an Aryl Halide Blocking Group for Oxidative Coupling.
Wu X, Iwata T, Scharf A, Qin T, Reichl K, Porco Jr J
J Am Chem Soc. 2018; 140(18):5969-5975.
PMID: 29658717
PMC: 5943148.
DOI: 10.1021/jacs.8b02535.
Enantiospecific Solvolytic Functionalization of Bromochlorides.
Burckle A, Gal B, Seidl F, Vasilev V, Burns N
J Am Chem Soc. 2017; 139(38):13562-13569.
PMID: 28858493
PMC: 5987033.
DOI: 10.1021/jacs.7b07792.
Titanium redox catalysis: insights and applications of an earth-abundant base metal.
Davis-Gilbert Z, Tonks I
Dalton Trans. 2017; 46(35):11522-11528.
PMID: 28795719
PMC: 5593795.
DOI: 10.1039/c7dt02319g.
Synthesis of malhamensilipin A exploiting iterative epoxidation/chlorination: experimental and computational analysis of epoxide-derived chloronium ions.
Saska J, Lewis W, Paton R, Denton R
Chem Sci. 2017; 7(12):7040-7049.
PMID: 28337338
PMC: 5282550.
DOI: 10.1039/c6sc03012b.
Highly Regio- and Enantioselective Vicinal Dihalogenation of Allyl Amides.
Soltanzadeh B, Jaganathan A, Yi Y, Yi H, Staples R, Borhan B
J Am Chem Soc. 2017; 139(6):2132-2135.
PMID: 28112919
PMC: 7790169.
DOI: 10.1021/jacs.6b09203.
Selective bromochlorination of a homoallylic alcohol for the total synthesis of (-)-anverene.
Seidl F, Burns N
Beilstein J Org Chem. 2016; 12:1361-5.
PMID: 27559385
PMC: 4979643.
DOI: 10.3762/bjoc.12.129.
A Unified Approach for the Enantioselective Synthesis of the Brominated Chamigrene Sesquiterpenes.
Burckle A, Vasilev V, Burns N
Angew Chem Int Ed Engl. 2016; 55(38):11476-9.
PMID: 27506430
PMC: 5505624.
DOI: 10.1002/anie.201605722.
Catalytic Enantioselective Dihalogenation and the Selective Synthesis of (-)-Deschloromytilipin A and (-)-Danicalipin A.
Landry M, Hu D, McKenna G, Burns N
J Am Chem Soc. 2016; 138(15):5150-8.
PMID: 27018981
PMC: 4922634.
DOI: 10.1021/jacs.6b01643.
Stereoselective Halogenation in Natural Product Synthesis.
Chung W, Vanderwal C
Angew Chem Int Ed Engl. 2016; 55(14):4396-434.
PMID: 26833878
PMC: 6028003.
DOI: 10.1002/anie.201506388.
Catalytic, Stereoselective Dihalogenation of Alkenes: Challenges and Opportunities.
Cresswell A, Eey S, Denmark S
Angew Chem Int Ed Engl. 2015; 54(52):15642-82.
PMID: 26630449
PMC: 5072131.
DOI: 10.1002/anie.201507152.
