Nile S. Abularrage
Affiliations: | 2022 | Massachusetts Institute of Technology, Cambridge, MA, United States |
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Publications
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Levandowski BJ, Graham BJ, Abularrage NS, et al. (2024) Taming the 1,5-sigmatropic shift across protonated spirocyclic 4-pyrazoles. Journal of Physical Organic Chemistry. 37 |
Levandowski BJ, Abularrage NS, Graham BJ, et al. (2023) Computational study of an oxetane 4-pyrazole as a Diels-Alder diene. Tetrahedron Letters. 130 |
Abularrage NS, Levandowski BJ, Giancola JB, et al. (2023) Bioorthogonal 4-pyrazole "click" reagents. Chemical Communications (Cambridge, England). 59: 4451-4454 |
Levandowski BJ, Abularrage NS, Raines RT. (2022) Spirocyclization enhances the Diels-Alder reactivities of geminally substituted cyclopentadienes and 4-pyrazoles. Journal of Physical Organic Chemistry. 36 |
Levandowski BJ, Abularrage NS, Raines RT. (2021) Geminal Repulsion Disrupts Diels-Alder Reactions of Geminally Substituted Cyclopentadienes and 4-Pyrazoles. Tetrahedron. 91 |
Dones JM, Abularrage NS, Khanal N, et al. (2021) Acceleration of 1,3-Dipolar Cycloadditions by Integration of Strain and Electronic Tuning. Journal of the American Chemical Society |
Levandowski BJ, Abularrage NS, Raines RT. (2020) Differential Effects of Nitrogen Substitution in 5‐ and 6‐Membered Aromatic Motifs Chemistry: a European Journal. 26: 8833-8833 |
Abularrage NS, Levandowski BJ, Raines RT. (2020) Synthesis and Diels-Alder Reactivity of 4-Fluoro-4-Methyl-4-Pyrazoles. International Journal of Molecular Sciences. 21 |
Levandowski BJ, Abularrage NS, Raines RT. (2020) Differential Effects of Nitrogen-Substitution in 5- and 6-Membered Aromatic Motifs. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Levandowski BJ, Abularrage NS, Houk KN, et al. (2019) Hyperconjugative Antiaromaticity Activates 4-Pyrazoles as Inverse-Electron-Demand Diels-Alder Dienes. Organic Letters. 21: 8492-8495 |