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Publications

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19. DiMucci, I.; Titus, C.; Nordlund, D.; Bour, J.; Chong, E.; Kosobokov, M.; Martin, C.; Nebra, N.; Vicic, D.; Yruegas, S.; MacMillan, S.; Shearer, J.; Lancaster, K. Scrutinizing Formally NiIV Centers through the Lenses of Core Spectroscopy, Molecular Orbital Theory, and Valence Bond Theory. Chem Rxiv. 2022.

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18. Yruegas, S.; Paccagnini, M. Ho, S. C.; Sattler, A.; Chirik, P. J. Nickel-Catalyzed Dimerization of Di- and Trisubstituted Olefins. Organometallics. 2022, 15, 2059–2066.

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17. Yruegas, S.; Semproni, S. P.; Chirik, P. J. (PNP)Cobalt-Catalyzed Olefination of Diazoalkanes. Organometallics. 2022, 41, 3138–3144.

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16. Yruegas, S.; Tang, H.; Bornovski, G. Z.; Su, X.; Sung, S.; Hall, M. B.; Nippe, M.; Martin, C. D., Nickel–Borolide Complexes and Their Complex Electronic Structure. Inorg. Chem. 2021, 21, 16160–16167.

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15. Su, X.§; Bartholome, T. A.§; Tidwell, J. R., Pujol, A., Yruegas, S.; Martinez, J. J.; Martin, C. D., 9-Borafluorenes: Synthesis, Properties, and Reactivity. Chem. Rev. 2021, 121, 4147-4192.

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14. Léonard, N. G.; Yruegas, S.; Ho, S. C.; Sattler, A.; Bezdek, M. J.; Chirik, P. J., Synthesis of Cationic, Dimeric α-Diimine Nickel Hydride Complexes and Relevance to the Polymerization of Olefins. Organometallics. 2020, 39, 2630–2635.

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13, Lambert, K. M.; Cox, J. B.; Liu, L.; Jackson, A. C.; Yruegas, S.; Wiberg, K. B.; Wood, J. L., Total Synthesis of (±)-Phyllantidine: Development and Mechanistic Evaluation of a Novel Ring Expansion for Installation of Embedded Nitrogen-Oxygen Bonds. Angew. Chem. Int. Ed. 2020, 59, 9757-9766

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12. Yruegas, S.; Axtell, J. C.; Kirlikovali, K. O.; Spokoyny, A. M.; Martin, C. D, Synthesis of 9-Borafluorene Analogues Featuring a Three-Dimensional 1,1’-Bis(o-carborane) Backbone. Chem. Commun. 2019, 55, 2892-2895 (Featured on the Front Cover).

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11. Laperriere, L. E.; Yruegas, S.; Martin, C. D., Investigating the Reactivity of 9-Phenyl-9-Borafluorene with N-H, O-H, P-H, and S-H Bonds. Tetrahedron. 2019, 75, 937-943 (Special Issue on Frustrated Lewis Acids and Organoboranes).

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10. Bluer, K. R.; Laperriere, L. E.; Pujol, A.; Yruegas, S.; Adiraju, V. A. K.; Martin, C. D., Coordination and Ring Expansion of 1,2-Dipolar Molecules with 9-Phenyl-9-borafluorene. Organometallics. 2018, 37, 2917-2927.

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9.  Yruegas, S.; Barnard, J. H.; Al-Furaiji, K.; Dutton, J. L; Wilson, D. J. D; Martin, C. D., Boraphosphaalkene Synthesis via Phosphaalkyne Insertion into 9-Borafluorene. Organometallics. 2018, 37, 1515-1518.

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8. Zhu, C.-L.; Wang, C.; Qin, Q.-X.; Yruegas, S.; Martin, C. D.; Xu, H., Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis. ACS Catal. 2018, 5032–5037. 

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7.  Yruegas, S.; Martinez, J. J.; Martin, C. D., Intermolecular Insertion Reactions of Azides Into 9-Borafluorenes to Generate 9,10-B,N-Phenanthrenes. Chem. Commun. 2018, 54, 6808-6811

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6.  Yruegas, S.; Wilson, C.; Dutton, J. L.; Martin, C. D., Ring Opening of Epoxides Induced by Pentaphenylborole. Organometallics. 2017, 36, 2581-2587 (Invited for Special Issue Entitled “Tailoring the Optoelectronic Properties of Organometallic Compounds with Main Group Elements”).

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5.  Yruegas, S.; Martin, C. D., Expedient Synthesis of 1,2-Thiaborines by means of Sulfur Insertion into Boroles. Chem. Eur. J. 2016, 22, 18358-18361 (Selected as a Hot Paper).

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4.   Barnard, J. H.; Yruegas, S.; Huang, K.; Martin, C. D., Ring expansion reactions of anti-aromatic boroles: a promising synthetic avenue to unsaturated boracycles. Chem. Commun. 2016, 52, 9985-9991 (Featured on the Inside Cover).

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3.  Yruegas, S.; Patterson, D. C.; Martin, C. D., Oxygen insertion into boroles as a route to 1,2-oxaborines. Chem. Commun. 2016, 52, 6658-6661 (Featured on the Inside Cover).

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2.  Barnard, J. H.; Yruegas, S.; Couchman, S. A.; Wilson, D. J. D.; Dutton, J. L.; Martin, C. D., Reactivity of a Phosphaalkyne with Pentaarylboroles. Organometallics. 2016, 35, 929–931

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1. Yruegas, S.; Huang, K.; Wilson, D. J. D.; Dutton, J. L.; Martin, C. D., Probing the reactivity of pentaphenylborole with N-H, O-H, P-H, and S-H bonds. Dalton Trans. 2016, 45, 9902-9911.

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