Matthew S Galliher
Overview
Explore the profile of Matthew S Galliher including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
88
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Recent Articles
1.
Roldan B, Hammerstad T, Galliher M, Keylor M, Pratt D, Stephenson C
Angew Chem Int Ed Engl
. 2023 Jun;
62(34):e202305801.
PMID: 37390358
A simple method for accessing trans-2,3-diaryl dihydrobenzofurans is reported. This approach leverages the equilibrium between quinone methide dimers and their persistent radicals. This equilibrium is disrupted by phenols that yield...
2.
Galliher M, Roldan B, Stephenson C
Chem Soc Rev
. 2021 Aug;
50(18):10044-10057.
PMID: 34350919
The use of radicals as intermediates in total synthesis has evolved since their initial use in the latter half of the twentieth century. Radical generation from metal hydride methodologies has...
3.
Raycroft M, Chauvin J, Galliher M, Romero K, Stephenson C, Pratt D
Chem Sci
. 2020 Aug;
11(22):5676-5689.
PMID: 32832049
Hydrogen atom transfer (HAT) is the mechanism by which the vast majority of radical-trapping antioxidants (RTAs), such as hindered phenols, inhibit autoxidation. As such, at least one weak O-H bond...
4.
Romero K, Galliher M, Raycroft M, Chauvin J, Bosque I, Pratt D, et al.
Angew Chem Int Ed Engl
. 2018 Nov;
57(52):17125-17129.
PMID: 30474921
A simple method for the dimerization of phenylpropenoid derivatives is reported. It leverages electrochemical oxidation of p-unsaturated phenols to access the dimeric materials in a biomimetic fashion. The mild nature...
5.
Romero K, Galliher M, Pratt D, Stephenson C
Chem Soc Rev
. 2018 Aug;
47(21):7851-7866.
PMID: 30101272
Free radical intermediates have intrigued chemists since their discovery, and an ever-increasing appreciation for their unique reactivity has resulted in the widespread utilization of these species throughout the field of...
6.
Dannoon S, Ganguly T, Cahaya H, Geruntho J, Galliher M, Beyer S, et al.
J Med Chem
. 2016 May;
59(12):5684-94.
PMID: 27228467
A series of phosphoramidate-based prostate specific membrane antigen (PSMA) inhibitors of increasing lipophilicity were synthesized (4, 5, and 6), and their fluorine-18 analogs were evaluated for use as positron emission...