F Dean Toste
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Explore the profile of F Dean Toste including associated specialties, affiliations and a list of published articles.
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292
Citations
6652
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Recent Articles
1.
Xia K, Toste F, Francis M, Baranger A
Chem Sci
. 2025 Feb;
16(10):4412-4429.
PMID: 39916887
Science's broader impacts and the historic social, political, and geographic implications of these impacts are rarely discussed in graduate STEM curricula. A new required "Scientific Responsibility and Citizenship" course for...
2.
Xie X, Moon P, Crossley S, Bischoff A, He D, Li G, et al.
Nature
. 2025 Jan;
637(8047):E24.
PMID: 39748037
No abstract available.
3.
Chung H, Schramm T, Head-Gordon M, Shee J, Toste F
J Am Chem Soc
. 2025 Jan;
147(2):2115-2128.
PMID: 39746122
Developing multicharge and spin stabilization strategies is fundamental to enhancing the lifetime of functional organic materials, particularly for long-term energy storage in multiredox organic redox flow batteries. Current approaches are...
4.
Huang B, Mai B, Warzok U, Liu P, Toste F
Tetrahedron Lett
. 2025 Jan;
149.
PMID: 39744146
Neutral dual hydrogen bond donors (HBDs) are effective catalysts that enhance the electrophilicity of substrates or the Lewis/Brønsted acidity of reagents through an anion-binding mechanism. Despite their success in various...
5.
Skakuj K, Iglhaut M, Shao Q, Garcia F, Huang B, Brittain S, et al.
Angew Chem Int Ed Engl
. 2024 Nov;
64(4):e202415976.
PMID: 39509590
Controlled modifications of amino acids are an indispensable tool for advancing fundamental and translational research based on peptides and proteins. Yet, we still lack methods to chemically modify each naturally...
6.
Treacy S, Smith A, Bergman R, Raymond K, Toste F
J Am Chem Soc
. 2024 Oct;
146(43):29792-29800.
PMID: 39432827
Catalysis of multicomponent transformations requires controlled assembly of reactants within the active site. Supramolecular scaffolds possess synthetic microenvironments that enable precise modulation over noncovalent interactions (NCIs) engaged by reactive, encapsulated...
7.
Dalton D, Walroth R, Rouget-Virbel C, Mack K, Toste F
J Am Chem Soc
. 2024 May;
146(23):15779-15786.
PMID: 38804885
Utopia Point Bayesian Optimization (UPBO) was used to identify reaction conditions that are highly selective for the formation of N1 and N2-methyl-3-aryl pyrazole constitutional isomers. UPBO was used to explore...
8.
Tracy J, Broderick C, Toste F
J Am Chem Soc
. 2024 Apr;
146(17):11740-11755.
PMID: 38629752
Nonaqueous organic redox flow batteries (N-ORFBs) are a promising technology for grid-scale storage of energy generated from intermittent renewable sources. Their primary benefit over traditional aqueous RFBs is the wide...
9.
Chen Y, Zhang R, Chen Z, Liao J, Song X, Liang X, et al.
J Am Chem Soc
. 2024 Apr;
146(15):10847-10856.
PMID: 38583085
Transition-metal-catalyzed carbene insertion reactions of a nitrogen-hydrogen bond have emerged as robust and versatile methods for the construction of C-N bonds. While significant progress of homogeneous catalytic metal carbene N-H...
10.
Haas B, Lim N, Jermaks J, Gaster E, Guo M, Malig T, et al.
J Am Chem Soc
. 2024 Mar;
146(12):8536-8546.
PMID: 38480482
Methods to access chiral sulfur(VI) pharmacophores are of interest in medicinal and synthetic chemistry. We report the desymmetrization of unprotected sulfonimidamides via asymmetric acylation with a cinchona-phosphinate catalyst. The desired...