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Publications
A Para-Selective Kolbe-Schmitt Reaction
X. Liu, G. J. P. Perry,* D. Kong*
Angew. Chem. Int. Ed. 2025, early view
Highlighted as a Hot Topic/Hot Paper
Photoredox Catalysed Reductive Cleavage of Dibenzothiophene Dioxides Enabled by a Temperature-Controlled Photoreactor
S. Wang, Q. T. Le, Y. Shishido, I. Y. Kokculer, K. Yamazaki, G. J. P. Perry*, A. M. Nightingale,* H. Yorimitsu*
Chem. Sci. 2025, 16, 23246 - 23252
DOI: 10.1039/D5SC05889A
Carboxylic Acid Salts as Dual-Function Reagents for Carboxylation and Carbon Isotope Labeling
S. Wang, I. Larrosa, H. Yorimitsu,* G. J. P. Perry*
Angew. Chem. Int. Ed. 2023, 62, e202218371
Highlighted in Org. Process Res. Dev. 2024, 28, 805–815
Highlighted as a Team Profile in Angew. Chem. Int. Ed. 2023, 62, e202306072
Late-Stage Sulfonic Acid/Sulfonate Formation from Sulfonamides via Sulfonyl Pyrroles
T. Ozaki, H. Yorimitsu,* G. J. P. Perry*
Tetrahedron 2022, 117-118, 132830
DOI: 10.1016/j.tet.2022.132830
Highlighted in Synfacts 2022, 18(09): 0956
Primary Sulfonamide Functionalization via Sulfonyl Pyrroles: Seeing the N−Ts Bond in a Different Light
T. Ozaki, H. Yorimitsu,* G. J. P. Perry*
Chem. Eur. J. 2021, 27, 15387-15391
Other Publications
Sulfur (IV) in Transition-Metal-Free Cross-Couplings for Biaryl Synthesis
G. J. P. Perry,* H. Yorimitsu*
ACS Sus. Chem. Eng. 2022, 10, 2569-2586
DOI: 10.1021/acssuschemeng.1c08673
Zincation of Styrylsulfonium Salts
K. Yamada, M. B. Kintzel, G. J. P. Perry, H. Saito, H. Yorimitsu
Org. Lett. 2022, 24, 7446-7449
DOI: 10.1021/acs.orglett.2c03013
Sulfonium-Aided Coupling of Aromatic Rings via Sigmatropic Rearrangement
G. J. P. Perry, H. Yorimitsu
Proc. Jpn. Acad., Ser. B 2022, 98, 190-205
DOI: 10.2183/pjab.98.012
Identification of Stomatal-Regulating Molecules from de novo Arylamine Collection through Aromatic C–H Amination
Y. Toda, G. J. P. Perry, S. Inoue, E. Ito, T. Kawakami, M. R Narouz, K. Takahashi, Y. Aihara, B. Maeda, T. Kinoshita, K. Itami,
K. Murakami
Sci. Rep. 2022, 12, 949
DOI: 10.1038/s41598-022-04947-z
Modular Synthesis of Unsymmetrical [1]Benzothieno[3,2-b][1]benzothiophene Molecular Semiconductors for Organic Transistors
M. Tayu, A. Rahmanudin, G. J. P. Perry, R. U. Khan, D. J. Tate, R. M.-Hernandez, Y. Shen, I. Dierking, Y. Janpatompong, S. Aphichatpanichakul, A. Zamhuri, I. Victoria-Yrezabal, M. L. Turner, D. J. Procter
Chem. Sci. 2022, 13, 421-429
DOI: 10.1039/D1SC05070B
Modular Synthesis of Stereodefined Benzocyclobutene Derivatives via Sequential Cu- and Pd-Catalysis
F. J. T. Talbot, S. Zhang, B. Satpathi, G. P. Howell, G. J. P. Perry, G. E. M. Crisenza, D. J. Procter
ACS. Catal. 2021, 11, 14448-14455
DOI: 10.1021/acscatal.1c04496
Enantioselective Copper-Catalyzed Borylative Cyclization for the Synthesis of Quinazolinones
Q. Dherbassy, S. Manna, C. Shi, W. Prasitwatcharakorn, G. E. M. Crisenza, G. J. P. Perry, D. J. Procter
Angew. Chem. Int. Ed. 2021, 60, 14355-14359
DOI: 10.1002/anie.202103259
Copper-Catalyzed Functionalization of Enynes
Q. Dherbassy, S. Manna, F. J. T. Talbot, W. Prasitwatcharakorn, G. J. P. Perry, D. J. Procter
Chem. Sci. 2020, 11, 11380-11393
DOI: 10.1039/D0SC04012F
Copper‐Catalyzed Borylative Couplings with C−N Electrophiles
F. J. T. Talbot, Q. Dherbassy, S. Manna, C. Shi, S. Zhang, G. P. Howell, G. J. P. Perry, D. J. Procter
Angew. Chem. Int. Ed. 2020, 59, 20278-20289
DOI: 10.1002/anie.202007251
Radical C–C Bond Formation using Sulfonium Salts and Light
A. Peter, G. J. P. Perry, D. J. Procter
Adv. Synth. Catal. 2020, 362, 2135-2142
DOI: 10.1002/adsc.202000220
Trifluoromethyl Sulfoxides: Reagents for Metal-Free C–H Trifluoromethylthiolation
D. Wang, C. G. Carlton, M. Tayu, J. J. W. McDouall, G. J. P. Perry, D. J. Procter
Angew. Chem. Int. Ed. 2020, 59, 15918-15922
DOI: 10.1002/anie.202005531
Para-Coupling of Phenols with C2/C3-Substituted Benzothiophene S-oxides
Z. He, T. Biremond, G. J. P. Perry, D. J. Procter
Tetrahedron 2020, 76, 131315
DOI: 10.1016/j.tet.2020.131315
Copper-Catalyzed Functionalization of 1,3-Dienes: Hydrofunctionalization, Borofunctionalization and Difunctionalization
G. J. P. Perry,* T. Jia, D. J. Procter*
ACS. Catal. 2020, 10, 1485-1499
DOI: 10.1021/acscatal.9b04767
Sulfoxide-Mediated Oxidative Cross-Coupling of Phenols
Z. He, G. J. P. Perry, D. J. Procter
Chem. Sci. 2020, 11, 2001-2005
DOI: 10.1039/C9SC05668H
Enantio- and Diastereoselectvie Synthesis of Homopropargyl Amines by Copper-Catalyzed Coupling of Imines, 1,3-Enynes and Diboranes
S. Manna, Q. Dherbassy, G. J. P. Perry, D. J. Procter
Angew. Chem. Int. Ed. 2020, 59, 4879-4882
DOI: 10.1002/anie.201915191
Metal-Free Photoredox-Catalyzed Formal C–H/C–H Coupling of Arenes Enabled by Interrupted Pummerer Activation
M. H. Aukland, M. Šiaučiulis, A. West, G. J. P. Perry, D. J. Procter
Nat. Catal. 2020, 3, 163-169
DOI: 10.1038/s41929-019-0415-3
Metal‐Free Synthesis of Benzothiophenes by Twofold C−H Functionalization: Direct Access to Materials‐Oriented Heteroaromatics
J. Yan, A. P. Pulis, G. J. P. Perry, D. J. Procter
Angew. Chem. Int. Ed. 2019, 58, 15675-15679
DOI: 10.1002/anie.201908319
Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes
T. Jia, M. J. Smith, A. P. Pulis, G. J. P. Perry, D. J. Procter
ACS Catal. 2019, 9, 6744-6750
DOI: 10.1021/acscatal.9b01911
Pummerer Chemistry of Benzothiophene S-oxides: Metal-Free Alkylation and Arylation of Benzothiophenes
Z. He, A. P. Pulis, G. J. P. Perry, D. J. Procter
Phosphorus Sulfur Silicon Relat. Elem. 2019, 194, 669-677
DOI: 10.1080/10426507.2019.1602626
Decarboxylative Suzuki–Miyaura Coupling of (Hetero)Aromatic Carboxylic Qcids Using Iodine as the Terminal Oxidant
J. M. Quibell, G. Duan, G. J. P. Perry, I. Larrosa
Chem. Commun. 2019, 55, 6445-6448
DOI: 10.1039/C9CC01817D
Transition-Metal-Free Synthesis of C3-Arylated Benzofurans from Benzothiophenes and Phenols
K. Yang, A. P. Pulis, G. J. P. Perry, D. J. Procter
Org. Lett. 2018, 20, 7498-7503
DOI: 10.1021/acs.orglett.8b03267
Transition-Metal-Free Decarboxylative Bromination of Aromatic Carboxylic Acids
J. M. Quibell, G. J. P. Perry, D. M. Cannas, I. Larrosa
Chem. Sci. 2018, 9, 3860-3865
DOI: 10.1039/C8SC01016A
The Use of Carboxylic Acids as Traceless Directing Groups for Regioselective C–H Bond Functionalisation
M. Font, J. M. Quibell, G. J. P. Perry, I. Larrosa
Chem. Commun. 2017, 53, 5584-5597
DOI: 10.1039/C7CC01755C
Transition-Metal-Free Decarboxylative Iodination: New Routes for Decarboxylative Oxidative Cross-Couplings
G. J. P. Perry, J. M. Quibell, A. Panigrahi, I. Larrosa
J. Am. Chem. Soc. 2017, 139, 11527-11536
DOI: 10.1021/jacs.7b05155
Recent Progress in Decarboxylative Oxidative Cross-Coupling for Biaryl Synthesis
G. J. P. Perry, I. Larrosa
Eur. J. Org. Chem. 2017, 2017, 3517-3527
DOI: 10.1002/ejoc.201700121
Aromatic C–H Amination: a Radical Approach for Adding New Functions into Biology- and Materials-Oriented Aromatics
K. Murakami, G. J. P. Perry, K. Itami
Org. Biomol. Chem. 2017, 15, 6071-6075
DOI: 10.1039/C7OB00985B
Ru-Catalyzed C–H Arylation of Fluoroarenes with Aryl Halides
M. Simonetti, G. J. P. Perry, X. C. Cambeiro, F. Juliá‐Hernández, J. N. Arokianathar, I. Larrosa
J. Am. Chem. Soc. 2016, 138, 3596-3606
DOI: 10.1021/jacs.6b01615
C–H Functionalisation of Heteroaromatic Compounds via Gold Catalysis
N. Ahlsten, X. C. Cambeiro, G. J. P. Perry, I. Larrosa
in Au-Catalyzed Synthesis and Functionalization of Heteroarenes (Topics in Heterocyclic Chemistry)
Springer: 2016; Vol. 46, pp 175-226
DOI: 10.1007/7081_2015_5005
A Silver-Free System for the Direct C–H Auration of Arenes and Heteroarenes from Gold Chloride Complexes
N. Ahlsten, G. J. P. Perry, X. C. Cambeiro, T. C. Boorman, I. Larrosa
Catal. Sci. Technol. 2013, 3, 2892-2897
DOI: 10.1039/C3CY00240C
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