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.
Li Y, Chen Z, Lin S, Liu Y, Qian J, Li Q
Adv Sci (Weinh). 2023; 10(30):e2304282.
PMID: 37632709
PMC: 10602563.
DOI: 10.1002/advs.202304282.
Gribble G
Prog Chem Org Nat Prod. 2023; 121:1-546.
PMID: 37488466
DOI: 10.1007/978-3-031-26629-4_1.
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.
Catalytic enantioselective bromohydroxylation of cinnamyl alcohols.
Li J, Shi Y
RSC Adv. 2022; 11(22):13040-13046.
PMID: 35423889
PMC: 8697332.
DOI: 10.1039/d1ra02297k.
The Electrochemical cis-Chlorination of Alkenes.
Strehl J, Fastie C, Hilt G
Chemistry. 2021; 27(69):17341-17345.
PMID: 34648232
PMC: 9297875.
DOI: 10.1002/chem.202103316.
Ritter-enabled catalytic asymmetric chloroamidation of olefins.
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.
Catalytic Dynamic Kinetic Resolutions in Tandem to Construct Two-Axis Terphenyl Atropisomers.
Beleh O, Miller E, Toste F, Miller S
J Am Chem Soc. 2020; 142(38):16461-16470.
PMID: 32857500
PMC: 7974015.
DOI: 10.1021/jacs.0c08057.
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.
Dative Directing Group Effects in Ti-Catalyzed [2+2+1] Pyrrole Synthesis: Chemo- and Regioselective Alkyne Heterocoupling.
Chiu H, See X, Tonks I
ACS Catal. 2019; 9(1):216-223.
PMID: 31768294
PMC: 6876699.
DOI: 10.1021/acscatal.8b04669.
Organoselenium-catalyzed enantioselective -dichlorination of unbiased alkenes.
Gilbert B, Eey S, Ryabchuk P, Garry O, Denmark S
Tetrahedron. 2019; 75(31):4086-4098.
PMID: 31768077
PMC: 6876749.
DOI: 10.1016/j.tet.2019.05.054.
Total Enzyme Syntheses of Napyradiomycins A1 and B1.
McKinnie S, Miles Z, Jordan P, Awakawa T, Pepper H, Murray L
J Am Chem Soc. 2018; 140(51):17840-17845.
PMID: 30525563
PMC: 6491662.
DOI: 10.1021/jacs.8b10134.
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.
Enantioselective Synthesis of Cyclobutenes by Intermolecular [2+2] Cycloaddition with Non-C Symmetric Digold Catalysts.
Garcia-Morales C, Ranieri B, Escofet I, Lopez-Suarez L, Obradors C, Konovalov A
J Am Chem Soc. 2017; 139(39):13628-13631.
PMID: 28922911
PMC: 5679663.
DOI: 10.1021/jacs.7b07651.
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.