Michael P Doyle
Affiliations: | The University of Texas at San Antonio, San Antonio, TX, United States |
Area:
catalysis, organic chemistryGoogle:
"Michael Doyle"Mean distance: (not calculated yet)
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Publications
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| De Angelis L, Haug GC, Rivera G, et al. (2023) Site Reversal in Nucleophilic Addition to 1,2,3-Triazine 1-Oxides. Journal of the American Chemical Society |
| Bao M, Doyle MP. (2023) Stereoretentive Catalytic [3 + 2]/[3 + 3]-Cycloaddition of Nonracemic Donor-Acceptor Cyclopropanes: Synthesis of Substituted Pyrrolidines and 1,2-Oxazinanes. Organic Letters. 25: 3029-3033 |
| De Angelis L, Pei C, Narro AL, et al. (2023) Polyfunctionalization of vicinal carbon centers and synthesis of unsymmetric 1,2,3,4-tetracarbonyl compounds. Nature Communications. 14: 1109 |
| Biswas S, De Angelis L, Rivera G, et al. (2023) Inverse Electron Demand Diels-Alder-Type Heterocycle Syntheses with 1,2,3-Triazine 1-Oxides: Expanded Versatility. Organic Letters |
| Bao M, Xie X, Huang J, et al. (2023) Divergent Construction of N-Doped Polycyclic Aromatic Hydrocarbons with Indole as the Nitrogen Source Building Block. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Rivera G, De Angelis L, Al-Sayyed A, et al. (2022) Synthesis of 1,2,3-Triazine Derivatives by Deoxygenation of 1,2,3-Triazine 1-Oxides. Organic Letters |
| Zheng H, Wang K, De Angelis L, et al. (2021) Brønsted Acid Catalyzed Oxocarbenium-Olefin Metathesis/Rearrangements of 1-Isochromene Acetals with Vinyl Diazo Compounds. Journal of the American Chemical Society |
| Liu S, Su YL, Sun TY, et al. (2021) Precise Introduction of the -CHX (X = F, Cl, Br, I) Moiety to Target Molecules by a Radical Strategy: A Theoretical and Experimental Study. Journal of the American Chemical Society |
| De Angelis L, Zheng H, Perz MT, et al. (2021) Intermolecular [5 + 1]-Cycloaddition between Vinyl Diazo Compounds and -Butyl Nitrite to 1,2,3-Triazine 1-Oxides and Their Further Transformation to Isoxazoles. Organic Letters |
| Joyasawal S, Ma D, Doyle MP. (2021) Challenges in the Highly Selective [3 + 1]-Cycloaddition of an Enoldiazoacetamide to Form a Donor-Acceptor -Cyclobutenecarboxamide. Molecules (Basel, Switzerland). 26 |