Horbaczewskyj C, Fairlamb I
Org Process Res Dev. 2022; 26(8):2240-2269.
PMID: 36032362
PMC: 9396667.
DOI: 10.1021/acs.oprd.2c00051.
Chen Z, Gu C, Yuen O, So C
Chem Sci. 2022; 13(17):4762-4769.
PMID: 35655875
PMC: 9067565.
DOI: 10.1039/d1sc06701j.
Elias E, Rehbein S, Neufeldt S
Chem Sci. 2022; 13(6):1618-1628.
PMID: 35282616
PMC: 8827013.
DOI: 10.1039/d1sc05862b.
Alvarez E, Karl T, Berger F, Torkowski L, Ritter T
Angew Chem Int Ed Engl. 2021; 60(24):13609-13613.
PMID: 33835680
PMC: 8251951.
DOI: 10.1002/anie.202103085.
Friggeri L, Hargrove T, Wawrzak Z, Guengerich F, Lepesheva G
J Med Chem. 2019; 62(22):10391-10401.
PMID: 31663733
PMC: 6881533.
DOI: 10.1021/acs.jmedchem.9b01485.
Suppressing Efficiency Roll-Off of TADF Based OLEDs by Constructing Emitting Layer With Dual Delayed Fluorescence.
Zhang Y, Li Z, Li C, Wang Y
Front Chem. 2019; 7:302.
PMID: 31114787
PMC: 6502957.
DOI: 10.3389/fchem.2019.00302.
Nickel-Catalyzed Stille Cross Coupling of C-O Electrophiles.
Russell J, Entz E, Joyce I, Neufeldt S
ACS Catal. 2019; 9(4):3304-3310.
PMID: 31057986
PMC: 6497415.
DOI: 10.1021/acscatal.9b00744.
Chemoselectivity in the Kosugi-Migita-Stille coupling of bromophenyl triflates and bromo-nitrophenyl triflates with (ethenyl)tributyltin.
Ansari N, Cummings M, Soderberg B
Tetrahedron. 2018; 74(21):2547-2560.
PMID: 30344349
PMC: 6193504.
DOI: 10.1016/j.tet.2018.02.051.
Direct catalytic cross-coupling of alkenyllithium compounds.
Hornillos V, Giannerini M, Vila C, Fananas-Mastral M, Feringa B
Chem Sci. 2018; 6(2):1394-1398.
PMID: 29560227
PMC: 5811103.
DOI: 10.1039/c4sc03117b.
Glycosyl Cross-Coupling of Anomeric Nucleophiles: Scope, Mechanism, and Applications in the Synthesis of Aryl C-Glycosides.
Zhu F, Rodriguez J, Yang T, Kevlishvili I, Miller E, Yi D
J Am Chem Soc. 2017; 139(49):17908-17922.
PMID: 29148749
PMC: 6581190.
DOI: 10.1021/jacs.7b08707.
Challenges and discoveries in the total synthesis of complex polyketide natural products.
Paterson I, Lam N
J Antibiot (Tokyo). 2017; 71(2):215-233.
PMID: 29066790
DOI: 10.1038/ja.2017.111.
Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol esters.
Laulhe S, Blackburn J, Roizen J
Chem Commun (Camb). 2017; 53(53):7270-7273.
PMID: 28345090
PMC: 5491353.
DOI: 10.1039/c7cc00997f.
Brominated Luciferins Are Versatile Bioluminescent Probes.
Steinhardt R, Rathbun C, Krull B, Yu J, Yang Y, Nguyen B
Chembiochem. 2016; 18(1):96-100.
PMID: 27930848
PMC: 5304417.
DOI: 10.1002/cbic.201600564.
An Expedient Total Synthesis of Chivosazole F: an Actin-Binding Antimitotic Macrolide from the Myxobacterium Sorangium Cellulosum.
Williams S, Jin J, Kan S, Li M, Gibson L, Paterson I
Angew Chem Int Ed Engl. 2016; 56(2):645-649.
PMID: 27897365
PMC: 6680201.
DOI: 10.1002/anie.201610636.
Pd- and Ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materials.
Xu S, Kim E, Wei A, Negishi E
Sci Technol Adv Mater. 2016; 15(4):044201.
PMID: 27877696
PMC: 5090684.
DOI: 10.1088/1468-6996/15/4/044201.
Stille coupling via C-N bond cleavage.
Wang D, Kawahata M, Yang Z, Miyamoto K, Komagawa S, Yamaguchi K
Nat Commun. 2016; 7:12937.
PMID: 27686744
PMC: 5056441.
DOI: 10.1038/ncomms12937.
A Mild and General Larock Indolization Protocol for the Preparation of Unnatural Tryptophans.
Chuang K, Kieffer M, Reisman S
Org Lett. 2016; 18(18):4750-3.
PMID: 27598827
PMC: 5505074.
DOI: 10.1021/acs.orglett.6b02477.
Selective and Serial Suzuki-Miyaura Reactions of Polychlorinated Aromatics with Alkyl Pinacol Boronic Esters.
Laulhe S, Blackburn J, Roizen J
Org Lett. 2016; 18(17):4440-3.
PMID: 27537216
PMC: 5433267.
DOI: 10.1021/acs.orglett.6b02323.
Studies toward the total synthesis of pluraflavin A.
Hartung J, J D Wright B, Danishefsky S
Chemistry. 2014; 20(28):8731-6.
PMID: 24919792
PMC: 4795151.
DOI: 10.1002/chem.201402254.
Studies toward the total synthesis of dihydrolycolucine. Preparation of AB and CEF ring fragments.
Cash B, Prevost N, Wagner F, Comins D
J Org Chem. 2014; 79(12):5740-5.
PMID: 24841361
PMC: 4066915.
DOI: 10.1021/jo500878v.