Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Matthew G. Donahue"'
Autor:
Matthew G. Donahue, Emily Crull
Publikováno v:
Molbank, Vol 2023, Iss 2, p M1650 (2023)
(R)-(+)-3,5-dinitro-N-(1-phenylethyl)benzothioamide 1 is a potential chiral solvating agent (CSA) for the spectral resolution of enantiomers via 1H NMR spectroscopy. The single enantiomer of 1 was synthesized from commercially available (R)-(+)-a-met
Externí odkaz:
https://doaj.org/article/d2f1b4c044c3482c980bbaec6afe5f33
Autor:
Long Phi Dinh, Jian Sun, Courtney D. Glenn, Krunal Patel, Julie A. Pigza, Matthew G. Donahue, Larry Yet, Jacques J. Kessl
Publikováno v:
Viruses, Vol 14, Iss 7, p 1466 (2022)
Allosteric HIV-1 integrase (IN) inhibitors, or ALLINIs, are a new class of antiviral agents that bind at the dimer interface of the IN, away from the enzymatic catalytic site and block viral replication by triggering an aberrant multimerization of th
Externí odkaz:
https://doaj.org/article/f2d416b3b3bc4289b2abab616bc72f4e
Autor:
Nicholas G. Jentsch, Jared D. Hume, Emily B. Crull, Samer M. Beauti, Amy H. Pham, Julie A. Pigza, Jacques J. Kessl, Matthew G. Donahue
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2529-2536 (2018)
A convenient two-step synthesis of ethyl 4-hydroxy-2-methylquinoline-3-carboxylate derivatives has been developed starting from commercially available 2-aminobenzoic acids. In step 1, the anthranilic acids are smoothly converted to isatoic anhydrides
Externí odkaz:
https://doaj.org/article/fbd91e864cd84c9da84a118b40063aa4
Autor:
Gavin J. Rustin, Matthew G. Donahue
Publikováno v:
Tetrahedron Letters. 122:154507
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::032c48c16095784d8d113c6898f2cef3
https://doi.org/10.1016/j.tetlet.2023.154507
https://doi.org/10.1016/j.tetlet.2023.154507
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 58:o1161-o1163
The title compound, C10H9NO3, exhibits near coplanarity of the phenyl ring with the C=O bond and the nitro group. Through the O atoms of the carbonyl and nitro groups and the H atoms of the phenyl rings, a network of intermolecular hydrogen bonds inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aede1022eaf239f59ac38435bb664bc0
https://doi.org/10.1107/s1600536802017142
https://doi.org/10.1107/s1600536802017142
Autor:
Matthew G. Donahue
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
1, R = Me[130267-88-8] C11H16SeSi (MW 255.29) InChI = 1S/C11H16SeSi/c1-13(2,3)10-9-12-11-7-5-4-6-8-11/h4-10H,1-3H3/b10-9+ InChIKey = FKHOLHHPSQIKEE-MDZDMXLPSA-N 2, R = Et [155623-70-4] C14H22SeSi (MW 297.37) InChI = 1S/C14H22SeSi/c1-4-16(5-2,6-3)13-1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad119e552f7bbc0d4a452b0e899c5bad
https://doi.org/10.1002/047084289x.rn01326
https://doi.org/10.1002/047084289x.rn01326
