Jeffrey W. Raggon
Affiliations: | 1986 | Chemistry | Michigan State University, East Lansing, MI |
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Li B, Magee TV, Buzon RA, et al. (2012) Process development of a novel azetidinyl ketolide antibiotic Organic Process Research and Development. 16: 788-797 |
Li B, Widlicka DW, Buzon RA, et al. (2010) A scaleable synthesis of 3-hydroxy-1,5-naphthyridine-4-carbaldehyde Synlett. 250-252 |
Andresen BM, Couturier M, Cronin B, et al. (2004) Streamlined processes for the synthesis of a farnesyl transferase inhibitor drug candidate Organic Process Research and Development. 8: 643-650 |
Ragan JA, Raggon JW, Hill PD, et al. (2003) Cross-coupling methods for the large-scale preparation of an imidazole - Thienopyridine: Synthesis of [2-(3-methyl-3H-imidazol-4-yl)-thieno[3,2-b]pyridin-7-yl] -(2-methyl-1H-indol-5-yl)-amine Organic Process Research and Development. 7: 676-683 |
Urban FJ, Jasys VJ, Raggon JW, et al. (2003) Novel Synthesis of 1-(1,2,3,5,6,7-Hexahydro-s-indacen-4-yl)-3- [4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonyl]urea, an Antiinflammatory Agent. Cheminform. 34 |
Tanis SP, Raggon JW. (1987) Pyrroles as terminators in cationic cyclizations. The preparation of 5,6,7,8-tetrahydroindolizidines and 6,7,8,9-tetrahydro-5H-pyrrolo[1,2-a]azepines The Journal of Organic Chemistry. 52: 819-827 |
TANIS SP, RAGGON JW. (1987) ChemInform Abstract: Pyrroles as Terminators in Cationic Cyclizations. The Preparation of 5,6,7,8-Tetrahydroindolizidines and 6,7,8,9-Tetrahydro-5H-pyrrolo-(1,2-a)azepines. Cheminform. 18 |
Hart H, Raggon JW. (1983) A significant new product from the addition of dichlorocarbene to tetraphenylcyclone Tetrahedron Letters. 24: 4891-4894 |
Rigby JH, Sage JM, Raggon J. (1982) A novel entry into the bicyclo[5.4.0]undecane ring system The Journal of Organic Chemistry. 47: 4815-4816 |
Rigby JH, Sage JM, Raggon J. (1982) A novel entry into the bicyclo[5.4.0]undecane ring system Journal of Organic Chemistry. 47: 4815-4816 |