Year |
Citation |
Score |
2022 |
Hopkins MD, Witt RC, Flusche AME, Philo JE, Ozmer GL, Purser GH, Sheaff RJ, Lamar AA. Synthesis and biological evaluation of -alkyl sulfonamides derived from polycyclic hydrocarbon scaffolds using a nitrogen-centered radical approach. Organic & Biomolecular Chemistry. PMID 35950721 DOI: 10.1039/d2ob01291j |
0.302 |
|
2021 |
Hopkins MD, Ozmer GL, Witt RC, Brandeburg ZC, Rogers DA, Keating CE, Petcoff PL, Sheaff RJ, Lamar AA. PhI(OAc) and iodine-mediated synthesis of -alkyl sulfonamides derived from polycyclic aromatic hydrocarbon scaffolds and determination of their antibacterial and cytotoxic activities. Organic & Biomolecular Chemistry. PMID 33443507 DOI: 10.1039/d0ob02429e |
0.565 |
|
2020 |
Rogers DA, Hopkins MD, Rajagopal N, Varshney D, Howard HA, LeBlanc G, Lamar AA. U.S. Food and Drug Administration-Certified Food Dyes as Organocatalysts in the Visible Light-Promoted Chlorination of Aromatics and Heteroaromatics. Acs Omega. 5: 7693-7704. PMID 32280913 DOI: 10.1021/acsomega.0c00631 |
0.563 |
|
2019 |
Hopkins MD, Abebe FA, Scott KA, Ozmer GL, Sheir AA, Schroeder LJ, Sheaff RJ, Lamar AA. Synthesis and identification of heteroaromatic N-benzyl sulfonamides as potential anticancer agents. Organic & Biomolecular Chemistry. PMID 31469373 DOI: 10.1039/C9Ob01694E |
0.4 |
|
2019 |
Rogers DA, Bensalah AT, Espinosa AT, Hoerr JL, Refai FH, Pitzel AK, Alvarado JJ, Lamar AA. Amplification of Trichloroisocyanuric Acid (TCCA) Reactivity for Chlorination of Arenes and Heteroarenes via Catalytic Organic Dye Activation. Organic Letters. PMID 31140821 DOI: 10.1021/Acs.Orglett.9B01414 |
0.614 |
|
2019 |
Rogers DA, Gallegos JM, Hopkins MD, Lignieres AA, Pitzel AK, Lamar AA. Visible-light photocatalytic activation of N-chlorosuccinimide by organic dyes for the chlorination of arenes and heteroarenes Tetrahedron. 75: 130498. DOI: 10.1016/J.Tet.2019.130498 |
0.638 |
|
2018 |
Rogers DA, Brown RG, Brandeburg ZC, Ko EY, Hopkins MD, LeBlanc G, Lamar AA. Organic Dye-Catalyzed, Visible-Light Photoredox Bromination of Arenes and Heteroarenes Using -Bromosuccinimide. Acs Omega. 3: 12868-12877. PMID 31458011 DOI: 10.1021/acsomega.8b02320 |
0.627 |
|
2018 |
Hopkins MD, Brandeburg ZC, Hanson AJ, Lamar AA. Visible-Light, Iodine-Promoted Formation of -Sulfonyl Imines and -Alkylsulfonamides from Aldehydes and Hypervalent Iodine Reagents. Molecules (Basel, Switzerland). 23. PMID 30042326 DOI: 10.3390/Molecules23081838 |
0.524 |
|
2017 |
Hopkins MD, Scott KA, DeMier BC, Morgan HR, Macgruder JA, Lamar AA. Formation of N-sulfonyl imines from iminoiodinanes by iodine-promoted, N-centered radical sulfonamidation of aldehydes. Organic & Biomolecular Chemistry. PMID 29077125 DOI: 10.1039/C7Ob02120H |
0.45 |
|
2016 |
Brueckner AC, Hancock EN, Anders EJ, Tierney MM, Morgan HR, Scott KA, Lamar AA. Visible-light-mediated, nitrogen-centered radical amination of tertiary alkyl halides under metal-free conditions to form α-tertiary amines. Organic & Biomolecular Chemistry. PMID 27113972 DOI: 10.1039/C6Ob00616G |
0.478 |
|
2015 |
Lamar AA, Liebeskind LS. Carboxyl activation via silylthioesterification: one-pot, two-step amidation of carboxylic acids catalyzed by non-metal ammonium salts. Tetrahedron Letters. 56: 6034-6037. PMID 37982035 DOI: 10.1016/j.tetlet.2015.09.050 |
0.416 |
|
2015 |
Lamar AA, Liebeskind LS. Carboxyl activation via silylthioesterification: One-pot, two-step amidation of carboxylic acids catalyzed by non-metal ammonium salts Tetrahedron Letters. 56: 6034-6037. DOI: 10.1016/J.Tetlet.2015.09.050 |
0.483 |
|
2010 |
Lamar AA, Nicholas KM. Iodine-catalyzed aminosulfonation of hydrocarbons by imidoiodinanes. A synthetic and mechanistic investigation. The Journal of Organic Chemistry. 75: 7644-50. PMID 20977281 DOI: 10.1021/Jo1015213 |
0.557 |
|
2009 |
Lamar AA, Nicholas KM. Direct synthesis of 3-arylindoles via annulation of aryl hydroxylamines with alkynes Tetrahedron. 65: 3829-3833. DOI: 10.1016/J.Tet.2009.03.004 |
0.565 |
|
2008 |
Kalita B, Lamar AA, Nicholas KM. Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons. Chemical Communications (Cambridge, England). 4291-3. PMID 18802547 DOI: 10.1039/B805783D |
0.555 |
|
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