Mele F, Constantin A, Porcheddu A, Maggi R, Maestri G, Ca N
Beilstein J Org Chem. 2025; 21:458-472.
PMID: 40041196
PMC: 11878148.
DOI: 10.3762/bjoc.21.33.
Lakhal A, Gimbert Y, Mouries-Mansuy V, Ollivier C, Fensterbank L
JACS Au. 2025; 5(2):448-465.
PMID: 40017740
PMC: 11862951.
DOI: 10.1021/jacsau.4c01040.
Yang L, Li S, Ning L, Zhao H, Zhou L, Cao W
Nat Commun. 2024; 15(1):10866.
PMID: 39738103
PMC: 11685906.
DOI: 10.1038/s41467-024-55110-3.
Dong B, Qi W, Chen Y, Zhang Y, Gu S, Zhao J
Adv Sci (Weinh). 2024; 12(2):e2411579.
PMID: 39573977
PMC: 11727398.
DOI: 10.1002/advs.202411579.
Hao P, Shi R, Wang X, Zhang J, Li B, Wang J
Sci Rep. 2024; 14(1):27057.
PMID: 39511277
PMC: 11543689.
DOI: 10.1038/s41598-024-78782-9.
Polymer semiconductor films and bacteria hybrid artificial bio-leaves.
Wen N, Jiang Q, Liu D
Sci Adv. 2024; 10(44):eadp8567.
PMID: 39485849
PMC: 11529708.
DOI: 10.1126/sciadv.adp8567.
Arylthianthrenium Salts for Triplet Energy Transfer Catalysis.
Cai Y, Roy T, Zahringer T, Lansbergen B, Kerzig C, Ritter T
J Am Chem Soc. 2024; 146(44):30474-30482.
PMID: 39466322
PMC: 11544621.
DOI: 10.1021/jacs.4c11099.
Visible-light-mediated deoxygenative transformation of 1,2-dicarbonyl compounds through energy transfer process.
Luo Y, Huang J, Wu G, Tang X, Qu J
Nat Commun. 2024; 15(1):9240.
PMID: 39455565
PMC: 11511947.
DOI: 10.1038/s41467-024-53635-1.
Counterion Effects in [Ru(bpy)](X)-Photocatalyzed Energy Transfer Reactions.
Zanzi J, Pastorel Z, Duhayon C, Lognon E, Coudret C, Monari A
JACS Au. 2024; 4(8):3049-3057.
PMID: 39211590
PMC: 11350745.
DOI: 10.1021/jacsau.4c00384.
Straightforward computational determination of energy-transfer kinetics through the application of the Marcus theory.
Sole-Daura A, Maseras F
Chem Sci. 2024; .
PMID: 39149213
PMC: 11322899.
DOI: 10.1039/d4sc03352c.
Photoinduced Single Electron Reduction of the 4-O-5 Linkage in Lignin Models for C-P Coupling Catalyzed by Bifunctional N-Heterocyclic Carbenes.
Liu Q, Ren Y, Zhang B, Tang W, Wang Z, He L
Adv Sci (Weinh). 2024; 11(38):e2406095.
PMID: 39099408
PMC: 11481192.
DOI: 10.1002/advs.202406095.
Charge-recombinative triplet sensitization of alkenes for DeMayo-type [2 + 2] cycloaddition.
Lee Y, Jhun B, Woo S, Kim S, Bae J, You Y
Chem Sci. 2024; 15(30):12058-12066.
PMID: 39092097
PMC: 11290448.
DOI: 10.1039/d4sc02601b.
Recent Progress in Free Radical Transformations of Allenamides.
Liu Y, Wang Z, Li R, Yao Y, Shi Z, Sun Q
Curr Org Synth. 2024; 21(7):889-902.
PMID: 39044703
DOI: 10.2174/0115701794269961231027054854.
Visible light-induced chemoselective 1,2-diheteroarylation of alkenes.
Guo S, Liu Y, Huang J, He L, He G, Ji D
Nat Commun. 2024; 15(1):6102.
PMID: 39030211
PMC: 11271625.
DOI: 10.1038/s41467-024-50460-4.
Photocatalytic systems: reactions, mechanism, and applications.
Mohamadpour F, Amani A
RSC Adv. 2024; 14(29):20609-20645.
PMID: 38952944
PMC: 11215501.
DOI: 10.1039/d4ra03259d.
Lattice Symmetry-Guided Charge Transport in 2D Supramolecular Polymers Promotes Triplet Formation.
Emmanuele R, Sai H, Chen J, Morrow D, dordevic L, Gosztola D
Adv Sci (Weinh). 2024; 11(30):e2402932.
PMID: 38864561
PMC: 11321616.
DOI: 10.1002/advs.202402932.
Recent advances in the application of [2 + 2] cycloaddition in the chemical synthesis of cyclobutane-containing natural products.
Hou S, Yan B, Sun H, Puno P
Nat Prod Bioprospect. 2024; 14(1):37.
PMID: 38861197
PMC: 11166626.
DOI: 10.1007/s13659-024-00457-9.
Isomerization of -Cinnamamides into -Cinnamamides Using a Recycling Photoreactor.
Suga M, Fukushima S, Makino K, Nakamura K, Tabata H, Oshitari T
J Org Chem. 2024; 89(12):8836-8844.
PMID: 38836790
PMC: 11197087.
DOI: 10.1021/acs.joc.4c00721.
Photochemical dearomative skeletal modifications of heteroaromatics.
Ji P, Duan K, Li M, Wang Z, Meng X, Zhang Y
Chem Soc Rev. 2024; 53(12):6600-6624.
PMID: 38817197
PMC: 11181993.
DOI: 10.1039/d4cs00137k.
Catalytic asymmetric [4 + 2] dearomative photocycloadditions of anthracene and its derivatives with alkenylazaarenes.
Tian D, Shi W, Sun X, Zhao X, Yin Y, Jiang Z
Nat Commun. 2024; 15(1):4563.
PMID: 38811663
PMC: 11137010.
DOI: 10.1038/s41467-024-48982-y.