Independent Publications
2024
13. A Radical Revolution in the 21st Century
A. Gómez‐Suárez,* S. P. Pitre,* C. Zhu* ChemCatChem 2024, e202401079
12. Modular Synthesis of Congested b2,2-Amino Acids via the Merger of Photocatalysis and Oxidative Functionalisations
K. Anwar, L. Capaldo, T. Wan, T. Noël, A. Gómez-Suárez* Chem. Commun., 2024, 60, 1456-1459
Preprint: ChemRxiv 2023 (DOI:10.26434/chemrxiv-2023-dbc9d)
One of the most read articles in Chem. Commun. in January 2024!
2023
11. Stereochemistry in All Its Shapes and Forms: The 56th Bürgenstock Conference
A. Gómez-Suárez,* and C. N. Neumann* Angew. Chem. Int. Ed. 2023, 62, e202309468
10. Modular Synthesis of Polar Spirocyclic Scaffolds Enabled by Radical Chemistry
K. Anwar, F. J. Aguilar Troyano,† A. H. Abazid,† O. El Yarroudi, I. Funes-Ardoiz, A. Gómez-Suárez* Org. Lett. 2023, 25, 3216–3221 (†These authors contributed equally)
Prepint version – ChemRxiv (DOI:10.26434/chemrxiv-2023-5jx42)
2022
9. Deoxygenative, Intramolecular Minisci-Type Reaction to Access Fused Heterocyclic Scaffolds
F. J. Aguilar Troyano,† K. Anwar,† F. Mohr, G. Robert, A. Gómez-Suárez* Eur. J. Org. Chem. 2022, 26, e202201176 (†These authors contributed equally)
8. Accessing α-Amino Ketyl Radicals from β-Amino Alcohols via Chemoselective Hydrogen Atom Transfer Catalysis
K. Merkens, N. Sanosa, I. Funes-Ardoiz, A. Gómez-Suárez* ACS Catal. 2022, 12, 13186–13192
Prepint version: ChemRxiv 10.26434/chemrxiv-2022-l6x03
7. Radical deoxyfunctionalisation strategies
K. Anwar,† K. Merkens,† F. J. Aguilar Troyano,† A. Gómez-Suárez* Eur. J. Org. Chem. 2022, 26, e202200330 (†These authors contributed equally)
6. Photocatalysis in the Life Science Industry
L. Candish,* K. D. Collins,* G. C. Cook, J. J. Douglas, A. Gómez-Suárez, A. Jolit, S. Kess Chem. Rev. 2022, 122, 2907–2980
2021
5. Synthesis of γ-oxo-α-amino acids via radical acylation with carboxylic Acids
K. Merkens,† F.J. Aguilar Troyano,† K. Anwar, A. Gómez-Suárez* J. Org. Chem. 2021, 12, 8448–8456 (†These authors contributed equally)
4. Radical‐Based Synthesis and Modification of Amino Acids
F.J. Aguilar Troyano,† K. Merkens,† K. Anwar, A. Gómez-Suárez* Angew. Chem. Int. Ed. 2021, 60, 1098-1115. (†These authors contributed equally)
2020
3. Selectfluor® Radical Dication (TEDA2+·) – A Versatile Species in Modern Synthetic Organic Chemistry
F.J. Aguilar Troyano,† K. Merkens,† A. Gómez-Suárez* Asian J. Org. Chem 2020, 9, 992-1007. (†These authors contributed equally)
2. Synthesis of Unnatural alpha-Amino Acid Derivatives via Light-mediated Radical Decarboxylative Processes
K. Merkens,† F.J. Aguilar Troyano,† J. Djossou, A. Gómez-Suárez* Adv. Synth. Catal. 2020, 362, 2354-2359 (†These authors contributed equally)
2019
1. Light‐mediated Formal Radical Deoxyfluorination of Tertiary Alcohols via Selective Single Electron Oxidation with TEDA2+·
F.J. Aguilar Troyano, F. Ballaschk,† M. Jaschinski,† Y. Ozkaya,† A. Gómez-Suárez* Chem. Eur. J. 2019, 25, 14054 (†These authors contributed equally)
BUW Publications – Kirsch Group
2024
4. anti-Dihydroxylation of olefins enabled by in situ generated peroxyacetic acid
M. Tapera, M. Chotia, J. L. Mayer-Figge, A. Gómez-Suárez,* S. F. Kirsch* Green Chem. 2024 DOI:10.1039/D4GC03540B
3. A Formal Synthesis of (+)-Hannokinol Using a Chiral Horner–Wittig Reagent
M. Tapera, F. Borghi, J. L. Mayer-Figge, F. Mittendorf, I.-E. Celik, A. Gómez-Suárez, S. F. Kirsch* Molecules 2024, 29, 3710
2. Formal synthesis of bastimolide A using a chiral Horner-Wittig reagent and a bifunctional aldehyde as key building blocks
I.-E. Celik, F. Mittendorf, A. Gómez-Suárez, S. F. Kirsch* Tetrahedron Chem 2024, 9, 100065
1. Oxidation of Alcohols in Continuous Flow with a Solid Phase Hypervalent Iodine Catalyst
K. Bensberg, A. Savvidis, F. Ballaschk, A. Gómez‐Suárez, S. F. Kirsch* Chem. Eur. J. 2024, 30, e202304011
PhD & Postdoc Publications
28. Discovery of Unforeseen Energy-Transfer-Based Transformations Using a Combined Screening Approach
F. Strieth-Kalthoff, C. Henkel, M. Teders, A. Kahnt, W. Knolle, A. Gómez-Suárez, K. Dirian, W. Alex, K. Bergander, C. G. Daniliuc, B. Abel, D. M. Guldi, F. Glorius, Chem. 2019, 5, 2183
27. The energy-transfer-enabled biocompatible disulfide–ene reaction
M. Teders, C. Henkel, L. Anhäuser, F. Strieth-Kalthoff, A. Gómez-Suárez, R. Kleinmans, A. Kahnt, A. Rentmeister, D. Guldi, F. Glorius, Nat. Chem. 2018, 10, 981.
26. Quantifying and understanding the steric properties of N-heterocyclic carbenes;
Gómez-Suárez, A.; Nelson, D. J.; Nolan, S. P., Chem. Commun. 2017, 53, 2650
25. Diverse visible light-promoted functionalizations of benzotriazoles inspired by mechanism-based luminescence screening
Teders, M.; Gómez-Suárez, A.+; Pitzer, L.+; Hopkinson, M. N.; Glorius, F., Angew. Chem. Int. Ed. 2016, 56, 902. +Both authors contributed equally.
24. A switchable gold catalyst by encapsulation in a self-assembled cage
Jans, A.; Gómez-Suárez, A.; Nolan, S. P.; Reek, J. N. H., Chem, Eur. J. 2016, 22, 14836
23. Catalytic access to alkyl bromides, chlorides and iodides via visible light-promoted decarboxylative halogenation
Candish, L.+; Standley, E. A.+; Gómez-Suárez, A.; Mukherjee, S.; Glorius, F., Chem, Eur. J. 2016, 22, 9971.
+Both authors contributed equally.
22. Accelerated discovery in photocatalysis using a mechanism-based screening method
Hopkinson, M. N.; Gómez-Suárez, A.; Teders, M.; Sahoo, B.; Glorius, F., Angew. Chem. Int. Ed. 2016, 55, 4361
- This paper was selected for the Angewandte front cover image “Catalyst Speed Dating!”.
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21. Visible light-promoted decarboxylative di- and trifluoromethylthiolation of alkyl carboxylic acids
Candish, L.+; Pitzer, L.+; Gómez-Suárez, A.; Glorius, F., Chem, Eur. J. 2016, 22, 4753.
+Both authors contributed equally.
20. Scope and limitations of the dual-gold-catalysed hydrophenoxylation of alkynes
Gómez-Suárez, A.; Oonishi, Y.; Martin, A. R.; Nolan, S. P. Beilstein J. Org. Chem. 2016, 12, 172
19. On the mechanism of the digold(I) hydroxide-catalysed hydrophenoxylation of alkynes
Gómez-Suárez, A.; Oonishi, Y.; Martin, A. R.; Vummaleti, S. V. C.; Nelson, D. J.; Cordes, D. B.; Slawin, A. M. Z.; Cavallo, L.; Nolan, S.P.; Poater, A.; Chem. Eur. J. 2016, 22, 1125
18. Gold-acetonyl complexes: from side-products to valuable synthons
Gasperini, D.; Collado, A.; Gómez-Suárez, A.; Cordes, D. B.; Slawin, A. M. Z.; Nolan, S. P. Chem. Eur. J. 2015, 21, 5403
17. What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Vummaleti, S. V. C.; Nelson, D. J.; Poater, A.; Gómez-Suárez, A.; Cordes, D. B.; Slawin, A. M. Z.; Nolan, S. P.; Cavallo, L., Chem. Sci. 2015, 6, 1895
16. [1,3-Bis[2,6-bis(1-methylethyl)phenyl]-2-imidazolidinylidene]chloro-gold
Gómez-Suárez, A.; Collado, A.; Nolan, S. P In e-EROS, Electronic Encyclopedia of Reagents for Organic Synthesis; John Wiley & Sons, Ltd.: Chichester, U.K., 2014.
15. [1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]chloro-gold
Collado, A.; Gómez-Suárez, A.; Nolan, S. P In e-EROS, Electronic Encyclopedia of Reagents for Organic Synthesis; John Wiley & Sons, Ltd.: Chichester, U.K., 2014.
14. [Au]/[Pd] multicatalytic process: direct one-pot access to benzo[c]chromenes and benzo[b]furans
Oonishi, Y.; Gómez-Suárez, A.; Martin, A. R.; Makida, Y.; Slawin, A. M. Z.; Nolan, S. P. Chem. Eur. J. 2014, 20, 13507
13. Trapping atmospheric CO2 with gold
Collado, A.; Gómez-Suárez, A.; Webb, P. B.; Kruger, H.; Bühl, M.; Cordes, D. B.; Slawin, A. M. Z.; Nolan, S. P. Chem. Commun. 2014, 50, 11321
12. Highly efficient and eco-friendly gold-catalyzed synthesis of homoallylic ketones
Gómez-Suárez, A.; Gasperini, D.; Vummaleti, S. V. C.; Poater, A.; Cavallo, L.; Nolan, S. P. ACS Catal. 2014, 2701.
11. New [Au(NHC)(OH)] complexes for silver-free protocols
Patrick, S. R.; Gómez-Suárez, A.; Slawin, A. M. Z.; Nolan, S. P. Organometallics 2013, 33, 421.
10. Synthesis, characterization and luminiscence studies of gold(I)-NHC amide complexes
Gómez-Suárez, A.; Nelson, D. J.; Thompson, D. G.; Cordes, D. B.; Graham, D.; Slawin, A. M. Z.; Nolan, S. P., Beilstein J. Org. Chem. 2013, 9, 2216.
9. Synthesis, characterisation, and oxygen atom transfer reactions involving the first gold(I)-alkylperoxo complexes
Collado, A.; Gómez-Suárez, A.; Slawin, A. M. Z.; Nolan, S. P. Chem. Commun. 2013, 49, 10745
8. Hydrophenoxylation of alkynes by cooperative gold catalysis
Oonishi, Y.; Gómez-Suárez, A.; Martin, A. R.; Nolan, S. P. Angew. Chem. Int. Ed. 2013, 52, 9767.
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7. Straightforward synthesis of [Au(NHC)X] (NHC = N-heterocyclic carbene, X = Cl, Br, I) complexes
Collado, A.; Gómez-Suárez, A.; Martin, A. R.; Slawin, A. M. Z.; Nolan, S. P. Chem. Commun. 2013, 49, 5541.
6. [{Au(NHC)}2(µ-OH)][BF4]: Silver-free and acid-free catalysts for water-inclusive gold-mediated organic transformations
Gómez-Suárez, A.; Oonishi, Y.; Meiries, S.; Nolan, S. P. Organometallics, 2013, 32, 1106
5. Straightforward synthetic access to gem-diaurated and digold σ,π-acetylide species
Gómez-Suárez, A.; Dupuy, S.; Slawin, A. M. Z.; Nolan, S. P. Angew. Chem. Int. Ed. 2013, 52, 938.
4. Dinuclear gold catalysis: are two gold centers better than one?
Gómez-Suárez, A.; Nolan, S. P. Angew. Chem. Int. Ed. 2012, 51, 8156.
3. Synthetic routes to [Au(NHC)(OH)] (NHC = N-heterocyclic carbene) complexes
Gómez-Suárez, A.; Ramón, R. S.; Slawin, A. M. Z.; Nolan, S. P. Dalton Trans. 2012, 41, 5461
2. Influence of a very bulky N-heterocyclic carbene in gold-mediated catalysis
Gómez-Suárez, A.; Ramón, R. S.; Songis, O.; Slawin, A. M. Z.; Cazin, C. S. J.; Nolan, S. P. Organometallics 2011, 30, 5463
1. Gold(I)-catalyzed tandem alkoxylation/lactonization of γ−hydroxy-α,β-acetylenic esters
Ramón, R. S.; Pottier, C.; Gómez-Suárez, A.; Nolan, S. P. Adv. Synth. Catal. 2011, 353, 1575
Book Chapters
Metallate Complexes of the Late Transition Metals: Organometallic Chemistry and Catalysis.
Gómez-Suárez, A.; Nelson, D. J.; Nolan, S. P., Metallate Complexes of the Late Transition Metals: Organometallic Chemistry and Catalysis. In Adv. Organomet. Chem., Academic Press: 2018.
Sustainable Homogeneous gold catalysis
Collado, A.; Gómez-Suárez, A.; and Nolan, S. P.; in Sustainable catalysis: with non-endangered metals, ed. North, M., The Royal Society of Chemistry, London, 2015, vol. 2, chp. 16.
