Timothy J. McAfoos, Ph.D.
Affiliations: | 2011 | Chemistry | Colorado State University, Fort Collins, CO |
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"Timothy McAfoos"Mean distance: 8.84 | S | N | B | C | P |
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Sign in to add mentorRobert Michael Williams | grad student | 2011 | Colorado State | |
(Studies on the biosynthesis of the stephacidins and notoamides. Total synthesis of notoamide S and notoamide T, and, Progress toward the synthesis of chrysogenamide A.) |
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Publications
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Dan Q, Newmister SA, Klas KR, et al. (2019) Fungal indole alkaloid biogenesis through evolution of a bifunctional reductase/Diels-Alderase. Nature Chemistry |
Kato H, Kai A, Kawabata T, et al. (2018) Corrigendum to "Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts" [Bioorg. Med. Chem. Lett. 27 (22) (2017) 4975-4978]. Bioorganic & Medicinal Chemistry Letters |
Kato H, Kai A, Kawabata T, et al. (2017) Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts. Bioorganic & Medicinal Chemistry Letters |
Sunderhaus JD, McAfoos TJ, Finefield JM, et al. (2013) Synthesis and bioconversions of notoamide T: a biosynthetic precursor to stephacidin A and notoamide B. Organic Letters. 15: 22-5 |
Li S, Anand K, Tran H, et al. (2012) Comparative analysis of the biosynthetic systems for fungal bicyclo[2.2.2]diazaoctane indole alkaloids: the (+)/(-)-notoamide, paraherquamide and malbrancheamide pathways. Medchemcomm. 3: 987-996 |
Li S, Finefield JM, Sunderhaus JD, et al. (2012) Biochemical characterization of NotB as an FAD-dependent oxidase in the biosynthesis of notoamide indole alkaloids. Journal of the American Chemical Society. 134: 788-91 |
Li S, Finefield JM, Sunderhaus JD, et al. (2012) Correction to “Biochemical Characterization of NotB as an FAD-Dependent Oxidase in the Biosynthesis of Notoamide Indole Alkaloids” Journal of the American Chemical Society. 134: 20565-20565 |
McAfoos TJ, Li S, Tsukamoto S, et al. (2010) STUDIES ON THE BIOSYNTHESIS OF THE STEPHACIDINS AND NOTOAMIDES. TOTAL SYNTHESIS OF NOTOAMIDE S. Heterocycles. 82: 461-472 |
Ding Y, de Wet JR, Cavalcoli J, et al. (2010) Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp. Journal of the American Chemical Society. 132: 12733-40 |