Steven P. Tanis
Affiliations: | 1980 | Chemistry | Columbia University, New York, NY |
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"Steven Tanis"Bio:
https://www2.chemistry.msu.edu/Genealogy/PID719.shtml
Mean distance: 7.97 | S | N | B | C | P |
Parents
Sign in to add mentorKoji Nakanishi | grad student | 1980 | Columbia | |
(I. The synthesis of some drimane sesquiterpenes. II. The structure of Harrisonin - an antifeedant limonoid from an East African Medicinal plant. III. Structural studies on the defensive secretions of Trinervitermes gratiosus, T. bettonianus, and Nasutiter) | ||||
David A. Evans | post-doc | 1979-1980 | Caltech |
Children
Sign in to add traineeDavid B. Head | grad student | 1985 | Michigan State |
Paul M. Herrinton | grad student | 1985 | Michigan State |
Yousef M. Abdallah | grad student | 1986 | Michigan State |
Benjamin A. Horenstein | grad student | 1986 | Michigan State |
Jeffrey W. Raggon | grad student | 1986 | Michigan State |
Yu Hwey Chuang | grad student | 1987 | Michigan State |
Lisa A. Dixon | grad student | 1988 | Michigan State |
Gary M. Johnson | grad student | 1989 | Michigan State |
Mark C. McMills | grad student | 1989 | Michigan State |
Edward D. Robinson | post-doc | 1993 | The Upjohn Company |
Mark A. Collins | post-doc | 1996 | The Upjohn Company |
Melissa V. Deaton | post-doc | 1997 | The Upjohn Company |
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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 |
Tanis SP, Colca JR, Parker TT, et al. (2018) PPARγ-sparing thiazolidinediones as insulin sensitizers. Design, synthesis and selection of compounds for clinical development. Bioorganic & Medicinal Chemistry |
Murphy ST, Alton G, Bailey S, et al. (2011) Discovery of novel, potent, and selective inhibitors of 3-phosphoinositide-dependent kinase (PDK1). Journal of Medicinal Chemistry. 54: 8490-500 |
Tanis SP, Strohbach JW, Parker TT, et al. (2010) The design and development of 2-aryl-2-hydroxy ethylamine substituted 1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamides as inhibitors of human cytomegalovirus polymerase. Bioorganic & Medicinal Chemistry Letters. 20: 1994-2000 |
Nair SK, Matthews JJ, Cripps SJ, et al. (2010) Novel synthesis of CP-734432, an EP4 agonist, using Sharpless asymmetric dihydroxylation Tetrahedron Letters. 51: 1451-1454 |
Schnute ME, Anderson DJ, Brideau RJ, et al. (2007) 2-Aryl-2-hydroxyethylamine substituted 4-oxo-4,7-dihydrothieno[2,3-b]pyridines as broad-spectrum inhibitors of human herpesvirus polymerases. Bioorganic & Medicinal Chemistry Letters. 17: 3349-53 |
Tanis SP, Evans BR, Nieman JA, et al. (2006) Solvent and in situ catalyst preparation impacts upon Noyori reductions of aryl-chloromethyl ketones: application to syntheses of chiral 2-amino-1-aryl-ethanols Tetrahedron Asymmetry. 17: 2154-2182 |
Tanis SP, Deaton MV, Dixon LA, et al. (1998) Furan-Terminated N-Acyliminium Ion Initiated Cyclizations in Alkaloid Synthesis. The Journal of Organic Chemistry. 63: 6914-6928 |
Tanis SP, Parker TT, Colca JR, et al. (1996) Synthesis and biological activity of metabolites of the antidiabetic, antihyperglycemic agent pioglitazone. Journal of Medicinal Chemistry. 39: 5053-63 |
Tanis SP, Robinson ED, McMills MC, et al. (1992) Furans in synthesis. 11. Total syntheses of (±)-and (-)-fastigilin C Journal of the American Chemical Society. 114: 8349-8362 |