Gerald D. Artman, Ph.D.
Affiliations: | 2004 | Pennsylvania State University, State College, PA, United States |
Area:
Total Synthesis of Natural ProductsGoogle:
"Gerald Artman"Mean distance: 8.27 | S | N | B | C | P |
Parents
Sign in to add mentor| Steven M. Weinreb | grad student | 2004 | Penn State | |
| (Part one. Studies on total synthesis of the cytotoxic marine alkaloid perophoramidine. Part two. Novel synthetic applications of the Hudson reaction.) | ||||
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Publications
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| Tanis SP, Colca JR, Parker TT, et al. (2019) The development of improved syntheses of PPARγ-sparing, insulin sensitizing thiazolidinedione-ketones Tetrahedron Letters. 60: 150931 |
| Ji N, Meredith E, Liu D, et al. (2010) Syntheses of 1-substituted-3-aminopyrazoles Tetrahedron Letters. 51: 6799-6801 |
| Artman GD, Solovay CF, Adams CM, et al. (2010) One-pot synthesis of 2-aminobenzimidazoles using 2-chloro-1,3- dimethylimidazolinium chloride (DMC) Tetrahedron Letters. 51: 5319-5321 |
| Jones DT, Artman GD, Williams RM. (2007) Coupling of activated esters to gramines in the presence of ethyl propiolate under mild conditions. Tetrahedron Letters. 48: 1291-1294 |
| Artman GD, Grubbs AW, Williams RM. (2007) Concise, asymmetric, stereocontrolled total synthesis of stephacidins A, B and notoamide B. Journal of the American Chemical Society. 129: 6336-42 |
| Seo JH, Artman GD, Weinreb SM. (2006) Synthetic studies on perophoramidine and the communesins: construction of the vicinal quaternary stereocenters. The Journal of Organic Chemistry. 71: 8891-900 |
| Artman GD, Weinreb SM. (2003) An approach to the total synthesis of the marine ascidian metabolite perophoramidine via a halogen-selective tandem Heck/carbonylation strategy. Organic Letters. 5: 1523-6 |
| Artman GD, Waldman JH, Weinreb SM. (2002) β-tosylethylhydroxylamine: Preparation and use as a hydroxylamine equivalent in amidyl radical-olefin cyclizations Synthesis. 2057-2063 |
| Artman GD, Bartolozzi A, Franck RW, et al. (2001) Preparation of N-sulfonylimines bearing easily removable protecting groups via the hudson reaction of oximes with sulfinyl chlorides Synlett. 232-233 |
| Lin X, Artman GD, Stien D, et al. (2001) Development of efficient new methodology for generation, cyclization and functional trapping of iminyl and amidyl radicals Tetrahedron. 57: 8779-8791 |