Skrypnik M, Kurtina D, Karamysheva S, Stepanidenko E, Vasileva I, Chang S
Nanomaterials (Basel). 2024; 14(23).
PMID: 39683309
PMC: 11643598.
DOI: 10.3390/nano14231921.
Yin Y, Wang J, Li J
Nat Commun. 2024; 15(1):2523.
PMID: 38514642
PMC: 10957970.
DOI: 10.1038/s41467-024-46960-y.
Gao Y, Jiang B, Friede N, Hunter A, Boucher D, Minteer S
J Am Chem Soc. 2024; 146(7):4872-4882.
PMID: 38324710
PMC: 11456316.
DOI: 10.1021/jacs.3c13442.
Kowalska E, Dyguda M, Artelska A, Albrecht A
J Org Chem. 2023; 88(23):16589-16597.
PMID: 38037694
PMC: 10696553.
DOI: 10.1021/acs.joc.3c02172.
Kawauchi G, Suga Y, Toda S, Hayashi Y
Chem Sci. 2023; 14(37):10081-10086.
PMID: 37772091
PMC: 10530343.
DOI: 10.1039/d3sc02978f.
Stereocontrolled Access to Quaternary Centers by Birch Reduction/Alkylation of Chiral Esters of Salicylic Acids.
Kozlowski R, Nguyen H, Lehman M, Vanderwal C
J Org Chem. 2023; 88(9):6232-6236.
PMID: 37040358
PMC: 10167686.
DOI: 10.1021/acs.joc.3c00306.
A General Catalyst Controlled Route to Prostaglandin F2.
Cunningham L, Mishra S, Matthews L, Fletcher S
Org Lett. 2022; 24(48):8886-8889.
PMID: 36446080
PMC: 9745796.
DOI: 10.1021/acs.orglett.2c03718.
An umpolung-enabled copper-catalysed regioselective hydroamination approach to α-amino acids.
Nishino S, Miura M, Hirano K
Chem Sci. 2021; 12(34):11525-11537.
PMID: 34567503
PMC: 8409476.
DOI: 10.1039/d1sc03692k.
Enantioenriched Positive Allosteric Modulators Display Distinct Pharmacology at the Dopamine D Receptor.
Fyfe T, Scammells P, Lane J, Capuano B
Molecules. 2021; 26(13).
PMID: 34206465
PMC: 8270344.
DOI: 10.3390/molecules26133799.
Pot and time economies in the total synthesis of Corey lactone.
Umekubo N, Suga Y, Hayashi Y
Chem Sci. 2021; 11(5):1205-1209.
PMID: 34123244
PMC: 8148033.
DOI: 10.1039/c9sc05824a.
Click Chemistry with Cyclopentadiene.
Levandowski B, Raines R
Chem Rev. 2021; 121(12):6777-6801.
PMID: 33651602
PMC: 8222071.
DOI: 10.1021/acs.chemrev.0c01055.
Lactones in the Synthesis of Prostaglandins and Prostaglandin Analogs.
Tanase C, Pintilie L, Tanase R
Int J Mol Sci. 2021; 22(4).
PMID: 33557221
PMC: 7913956.
DOI: 10.3390/ijms22041572.
Hierarchically assembled helicates as reaction platform - from stoichiometric Diels-Alder reactions to enamine catalysis.
Van Craen D, Begall J, Grosskurth J, Himmel L, Linnenberg O, Isaak E
Beilstein J Org Chem. 2020; 16:2338-2345.
PMID: 33029252
PMC: 7522461.
DOI: 10.3762/bjoc.16.195.
Facile Preparation of Spirolactones by an Alkoxycarbonyl Radical Cyclization-Cross-Coupling Cascade.
Weires N, Slutskyy Y, Overman L
Angew Chem Int Ed Engl. 2019; 58(25):8561-8565.
PMID: 30989757
PMC: 6555670.
DOI: 10.1002/anie.201903353.
Reductive α-borylation of α,β-unsaturated esters using NHC-BH activated by I as a metal-free route to α-boryl esters.
Radcliffe J, Fasano V, Adams R, You P, Ingleson M
Chem Sci. 2019; 10(5):1434-1441.
PMID: 30809360
PMC: 6354834.
DOI: 10.1039/c8sc04305a.
Remote C-H functionalization using radical translocating arylating groups.
Friese F, Muck-Lichtenfeld C, Studer A
Nat Commun. 2018; 9(1):2808.
PMID: 30022072
PMC: 6051993.
DOI: 10.1038/s41467-018-05193-6.
Stereopermutation on the Putative Structure of the Marine Natural Product Mucosin.
Antonsen S, Gallantree-Smith H, Gorbitz C, Hansen T, Stenstrom Y, Nolsoe J
Molecules. 2017; 22(10).
PMID: 29027970
PMC: 6151738.
DOI: 10.3390/molecules22101720.
Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol.
Crossley S, Martinez R, Guevara-Zuluaga S, Shenvi R
Org Lett. 2016; 18(11):2620-3.
PMID: 27175746
PMC: 5871529.
DOI: 10.1021/acs.orglett.6b01047.
Highly stereoselective synthesis of cyclopentanes bearing four stereocentres by a rhodium carbene-initiated domino sequence.
Parr B, Davies H
Nat Commun. 2014; 5:4455.
PMID: 25082301
PMC: 4149473.
DOI: 10.1038/ncomms5455.
Diastereoselective three-component synthesis of β-amino carbonyl compounds using diazo compounds, boranes, and acyl imines under catalyst-free conditions.
Luan Y, Yu J, Zhang X, Schaus S, Wang G
J Org Chem. 2014; 79(10):4694-8.
PMID: 24787904
PMC: 4033649.
DOI: 10.1021/jo5003505.