Cao R, Su R, Wei Z, Li Z, Zhu D, Huo Y
Nat Commun. 2025; 16(1):2147.
PMID: 40032867
PMC: 11876436.
DOI: 10.1038/s41467-025-57381-w.
Frank E, Park S, Harrer E, Flugel J, Fischer M, Nuernberger P
J Am Chem Soc. 2024; 146(50):34383-34393.
PMID: 39644236
PMC: 11664596.
DOI: 10.1021/jacs.4c09405.
Kalomenopoulos P, Emayavaramban B, Johnston C
Angew Chem Int Ed Engl. 2024; 64(2):e202414342.
PMID: 39312676
PMC: 11720393.
DOI: 10.1002/anie.202414342.
Soutome H, Yamashita H, Shimizu Y, Takumi M, Ashikari Y, Nagaki A
Nat Commun. 2024; 15(1):4873.
PMID: 38871696
PMC: 11176188.
DOI: 10.1038/s41467-024-48723-1.
Solano Y, Kiser P
Trends Biochem Sci. 2024; 49(8):703-716.
PMID: 38760195
PMC: 11780667.
DOI: 10.1016/j.tibs.2024.04.007.
Total Synthesis of Acanthodoral Using a Rearrangement Strategy.
Eggert A, Schuppe K, Fuchs H, Bronstrup M, Kalesse M
Org Lett. 2024; 26(15):2893-2896.
PMID: 38165657
PMC: 11041117.
DOI: 10.1021/acs.orglett.3c03717.
Unlocking mild-condition benzene ring contraction using nonheme diiron -oxygenase.
Guo Y, Tian Z, Ma C, Han Y, Bai D, Jiang Z
Chem Sci. 2023; 14(42):11907-11913.
PMID: 37920353
PMC: 10619644.
DOI: 10.1039/d3sc04660e.
Development of a microfluidic photochemical flow reactor concept by rapid prototyping.
Dinter R, Willems S, Nissalk T, Hasturk O, Brunschweiger A, Kockmann N
Front Chem. 2023; 11:1244043.
PMID: 37608867
PMC: 10441772.
DOI: 10.3389/fchem.2023.1244043.
Asymmetric Total Syntheses of Euphol and Tirucallol.
Nicholson J, Micalizio G
Org Lett. 2023; 25(30):5687-5691.
PMID: 37477981
PMC: 10654682.
DOI: 10.1021/acs.orglett.3c02187.
A Domino Radical Amidation/Semipinacol Approach to All-Carbon Quaternary Centers Bearing an Aminomethyl Group.
Dhak M, Arunprasath D, Argent S, Cuthbertson J
Chemistry. 2023; 29(47):e202300922.
PMID: 37278542
PMC: 10947466.
DOI: 10.1002/chem.202300922.
A convergent fragment coupling strategy to access quaternary stereogenic centers.
Kerkovius J, Wong A, Mak V, Reisman S
Chem Sci. 2023; 14(16):4397-4400.
PMID: 37123185
PMC: 10132171.
DOI: 10.1039/d2sc07023e.
A Convergent Total Synthesis of (+)-Ineleganolide.
Gross B, Han S, Virgil S, Stoltz B
J Am Chem Soc. 2023; 145(14):7763-7767.
PMID: 36989438
PMC: 10544024.
DOI: 10.1021/jacs.3c02142.
Expedient synthesis of spiro[3.3]heptan-1-ones via strain-relocating semipinacol rearrangements.
Jung M, Muir J, Lindsay V
Tetrahedron. 2023; 134.
PMID: 36937489
PMC: 10019042.
DOI: 10.1016/j.tet.2023.133296.
Synthesis of Dihydropyridine Spirocycles by Semi-Pinacol-Driven Dearomatization of Pyridines.
Abell J, Bold C, Vicens L, Jentsch T, Velasco N, Tyler J
Org Lett. 2023; 25(2):400-404.
PMID: 36626565
PMC: 9872164.
DOI: 10.1021/acs.orglett.2c04095.
Iminologous epoxide ring-closure.
Tien C, Lough A, Yudin A
Chem Sci. 2022; 13(41):12175-12179.
PMID: 36349099
PMC: 9600474.
DOI: 10.1039/d2sc04496j.
Toward the Asymmetric de Novo Synthesis of Lanostanes: Construction of 7,11-Dideoxy-Δ-lucidadone H.
Wai H, Micalizio G
J Org Chem. 2022; 87(21):14975-14979.
PMID: 36206482
PMC: 9662812.
DOI: 10.1021/acs.joc.2c02042.
Hydrogen-Bond-Modulated Nucleofugality of Se Species to Enable Photoredox-Catalytic Semipinacol Manifolds.
Park S, Dutta A, Allacher C, Abramov A, Dullinger P, Kuzmanoska K
Angew Chem Int Ed Engl. 2022; 61(49):e202208611.
PMID: 36111586
PMC: 10098919.
DOI: 10.1002/anie.202208611.
Single-atom logic for heterocycle editing.
Jurczyk J, Woo J, Kim S, Dherange B, Sarpong R, Levin M
Nat Synth. 2022; 1(5):352-364.
PMID: 35935106
PMC: 9355079.
DOI: 10.1038/s44160-022-00052-1.
Iron-Catalyzed Photoinduced LMCT: a 1° C-H Abstraction Enables Skeletal Rearrangements and C(sp)-H Alkylation.
Kang Y, Treacy S, Rovis T
ACS Catal. 2022; 11(12):7442-7449.
PMID: 35669035
PMC: 9164223.
DOI: 10.1021/acscatal.1c02285.
Organophotoredox-catalyzed semipinacol rearrangement via radical-polar crossover.
Kodo T, Nagao K, Ohmiya H
Nat Commun. 2022; 13(1):2684.
PMID: 35562383
PMC: 9106707.
DOI: 10.1038/s41467-022-30395-4.