Matthew A. Perry, Ph.D.
Affiliations: | 2013 | Chemistry - Ph.D. | University of California, Irvine, Irvine, CA |
Area:
Organic Chemistry, Synthesis and Structure DeterminationGoogle:
"Matthew Perry"Mean distance: 7.97 | S | N | B | C | P |
Parents
Sign in to add mentor| Scott D. Rychnovsky | grad student | 2013 | UC Irvine | |
| (alpha-Heteroatom Nitriles as Trianion Synthons: Synthesis of Spirocyclic Heterocycles and the Lepadiformine Alkaloids.) | ||||
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Publications
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| Conn EL, Perry MA, Shi K, et al. (2022) Identification of parallel medicinal chemistry protocols to expand branched amine design space. Organic & Biomolecular Chemistry |
| Zhao JX, Chang YX, He C, et al. (2021) 1,2-Difunctionalized bicyclo[1.1.1]pentanes: Long-sought-after mimetics for /-substituted arenes. Proceedings of the National Academy of Sciences of the United States of America. 118 |
| McCosker PM, Butler NM, Shakoori A, et al. (2020) The Cascade Reactions of Indigo with Propargyl Substrates for Heterocyclic and Photophysical Diversity. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Wright SW, Simpson B, Chinigo G, et al. (2020) Reduction of 2-hydroxy-3-arylmorpholines to 3-aryl morpholines Tetrahedron. 76: 131253 |
| Ni S, Muñoz Padial N, Kingston C, et al. (2019) A Radical Approach to Anionic Chemistry: Synthesis of Ketones, Alcohols, and Amines. Journal of the American Chemical Society |
| Campello HR, Parker J, Perry M, et al. (2016) Asymmetric Reduction of Lactam-Based β-Aminoacrylates. Synthesis of Heterocyclic β(2)-Amino Acids. Organic Letters |
| Perry MA, Hill RR, Leong JJ, et al. (2015) Stereochemical Outcomes in Reductive Cyclizations To Form Spirocyclic Heterocycles. Organic Letters. 17: 3268-71 |
| Perry MA, Rychnovsky SD. (2015) Generation, structure and reactivity of tertiary organolithium reagents. Natural Product Reports. 32: 517-33 |
| Perry MA, Hill RR, Rychnovsky SD. (2013) Trianion synthon approach to spirocyclic heterocycles. Organic Letters. 15: 2226-9 |
| Perry MA, Trinidad JV, Rychnovsky SD. (2013) Absolute configuration of lactams and oxazolidinones using kinetic resolution catalysts. Organic Letters. 15: 472-5 |