Year |
Citation |
Score |
2019 |
Tanis SP, Colca JR, Parker TT, Artman GD, Larsen SD, Gadwood RC, Zeller JR. The development of improved syntheses of PPARγ-sparing, insulin sensitizing thiazolidinedione-ketones Tetrahedron Letters. 60: 150931. DOI: 10.1016/J.Tetlet.2019.07.022 |
0.379 |
|
2018 |
Tanis SP, Colca JR, Parker TT, Artman GD, Larsen SD, McDonald WG, Gadwood RC, Kletzien RF, Zeller JB, Lee PH, Adams WJ. PPARγ-sparing thiazolidinediones as insulin sensitizers. Design, synthesis and selection of compounds for clinical development. Bioorganic & Medicinal Chemistry. PMID 30429097 DOI: 10.1016/J.Bmc.2018.10.033 |
0.306 |
|
2011 |
Murphy ST, Alton G, Bailey S, Baxi SM, Burke BJ, Chappie TA, Ermolieff J, Ferre R, Greasley S, Hickey M, Humphrey J, Kablaoui N, Kath J, Kazmirski S, Kraus M, ... ... Tanis SP, et al. Discovery of novel, potent, and selective inhibitors of 3-phosphoinositide-dependent kinase (PDK1). Journal of Medicinal Chemistry. 54: 8490-500. PMID 22040023 DOI: 10.1021/Jm201019K |
0.367 |
|
2010 |
Tanis SP, Strohbach JW, Parker TT, Moon MW, Thaisrivongs S, Perrault WR, Hopkins TA, Knechtel ML, Oien NL, Wieber JL, Stephanski KJ, Wathen MW. 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. PMID 20167488 DOI: 10.1016/J.Bmcl.2010.01.094 |
0.305 |
|
2010 |
Nair SK, Matthews JJ, Cripps SJ, Ma C, Dovalsantos EZ, Grubbs AW, Sach NW, Hoeve Wt, Koster H, Flahive EJ, Tanis SP, Renner M, Wiltenburg Jv. Novel synthesis of CP-734432, an EP4 agonist, using Sharpless asymmetric dihydroxylation Tetrahedron Letters. 51: 1451-1454. DOI: 10.1016/J.Tetlet.2009.12.092 |
0.417 |
|
2007 |
Schnute ME, Anderson DJ, Brideau RJ, Ciske FL, Collier SA, Cudahy MM, Eggen M, Genin MJ, Hopkins TA, Judge TM, Kim EJ, Knechtel ML, Nair SK, Nieman JA, Oien NL, ... ... Tanis SP, et al. 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. PMID 17434304 DOI: 10.1016/J.Bmcl.2007.03.102 |
0.314 |
|
2006 |
Tanis SP, Evans BR, Nieman JA, Parker TT, Taylor WD, Heasley SE, Herrinton PM, Perrault WR, Hohler RA, Dolak LA, Hester MR, Seest EP. 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. DOI: 10.1016/J.Tetasy.2006.07.017 |
0.399 |
|
1998 |
Tanis SP, Deaton MV, Dixon LA, McMills MC, Raggon JW, Collins MA. Furan-Terminated N-Acyliminium Ion Initiated Cyclizations in Alkaloid Synthesis. The Journal of Organic Chemistry. 63: 6914-6928. PMID 11672313 DOI: 10.1021/Jo980718L |
0.669 |
|
1996 |
Tanis SP, Parker TT, Colca JR, Fisher RM, Kletzein RF. Synthesis and biological activity of metabolites of the antidiabetic, antihyperglycemic agent pioglitazone. Journal of Medicinal Chemistry. 39: 5053-63. PMID 8978836 DOI: 10.1021/Jm9605694 |
0.318 |
|
1992 |
Tanis SP, Robinson ED, McMills MC, Watt W. Furans in synthesis. 11. Total syntheses of (±)-and (-)-fastigilin C Journal of the American Chemical Society. 114: 8349-8362. DOI: 10.1021/Ja00048A003 |
0.769 |
|
1990 |
Tanis SP, McMills MC, Scahill TA, Kloosterman DA. Furans in synthesis 101. An efficient construction of the bicyclo[5.3.0]decane ring system of fastigilin-C Tetrahedron Letters. 31: 1977-1980. DOI: 10.1016/S0040-4039(00)88893-0 |
0.733 |
|
1988 |
Tanis SP, Chuang YH, Head DB. Furans in synthesis. 8. Formal total syntheses of (.+-.)- and (+)-aphidicolin Journal of Organic Chemistry. 53: 4929-4938. DOI: 10.1021/Jo00256A007 |
0.76 |
|
1987 |
Tanis SP, Raggon JW. 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 Journal of Organic Chemistry. 52: 819-827. DOI: 10.1021/Jo00381A021 |
0.369 |
|
1987 |
Tanis SP, Dixon LA. Furans in synthesis.7. A formal total synthesis of (+/-)-perhydrohistrionicotoxin Tetrahedron Letters. 28: 2495-2498. DOI: 10.1016/S0040-4039(00)95450-9 |
0.659 |
|
1985 |
Tanis SP, McMills MC, Herrinton PM. A convenient synthesis of vinyl spiro epoxides from .alpha.,.beta.-unsaturated ketones The Journal of Organic Chemistry. 50: 5887-5889. DOI: 10.1021/Jo00350A097 |
0.71 |
|
1985 |
Tanis SP, Herrinton PM, Dixon LA. Furans in Synthesis. The Preparation of Spiro-Cyclic Systems. Tetrahedron Letters. 26: 5347-5350. DOI: 10.1016/S0040-4039(00)98204-2 |
0.759 |
|
1985 |
Tanis SP, Chuang YH, Head DB. A formal total synthesis of (±)-aphidicolin Tetrahedron Letters. 26: 6147-6150. DOI: 10.1016/S0040-4039(00)95038-X |
0.724 |
|
1985 |
Tanis SP, Abdallah YM, Williard PG. Selective rearrangements of 4a,5-epoxides of 4,4-dimethyl-1,2,3,4,6,8a-hexahydronaphthalenes. Tetrahedron Letters. 26: 3651-3654. DOI: 10.1016/S0040-4039(00)89214-X |
0.717 |
|
1985 |
Tanis SP, McMills MC, Herrinton PM. A convenient synthesis of vinyl spiro epoxides from α,β-unsaturated ketones Journal of Organic Chemistry. 50: 5887-5889. DOI: 10.1002/Chin.198630195 |
0.728 |
|
1985 |
Tanis SP, Herrinton PM. Furans in synthesis. 5. Furan-terminated cationic cyclizations in the preparation of fused, spirocyclic and bridged ring systems. An application to the synthesis of nakafuran 9 Journal of Organic Chemistry. 50: 3988-3996. |
0.392 |
|
1984 |
Tanis SP, Head DB. Furans in synthesis 4. Silyl furans as butenolide equivalents Tetrahedron Letters. 25: 4451-4454. DOI: 10.1016/S0040-4039(01)81464-7 |
0.729 |
|
1983 |
Tanis SP, Herrinton PM. Furans in synthesis. 3. Furans as terminators in cationic cyclization Journal of Organic Chemistry. 48: 4572-4580. |
0.407 |
|
1982 |
Tanis SP. A simple synthesis of 3-substituted furans. The preparations of dendrolasin, perillene and congeners Tetrahedron Letters. 23: 3115-3118. DOI: 10.1016/S0040-4039(00)88573-1 |
0.415 |
|
1982 |
Tanis SP, Head DB. Furans in Synthesis. The Preparation of (±)-Lactaral Tetrahedron Letters. 23: 5509-5512. DOI: 10.1016/S0040-4039(00)85880-3 |
0.734 |
|
1980 |
Akita H, Tanis SP, Adams M, Balogh-Nair V, Nakanishi K. Nonbleachable rhodopsins retaining the full natural chromophore Journal of the American Chemical Society. 102: 6370-6372. DOI: 10.1021/Ja00540A047 |
0.392 |
|
1979 |
Tanis SP, Nakanishi K. Stereospecific total synthesis of (.+-.)-warburganal and related compounds Journal of the American Chemical Society. 101: 4398-4400. DOI: 10.1021/Ja00509A071 |
0.515 |
|
1978 |
Tanis SP, Brown RH, Nakanishi K. A convenient synthesis of stereochemically pure retinoids. The synthesis of 10,14-dimethyl retinals. Tetrahedron Letters. 19: 869-872. DOI: 10.1016/S0040-4039(01)91422-4 |
0.535 |
|
1977 |
Prestwich GD, Solheim BA, Clardy J, Pilkiewicz FG, Miura I, Tanis SP, Nakanishi K. Kempene-1 and -2, unusual tetracyclic diterpenes from Nasutitermes termite soldiers Journal of the American Chemical Society. 99: 8082-8083. DOI: 10.1021/Ja00466A068 |
0.544 |
|
1976 |
Prestwich GD, Tanis SP, Pilkiewicz FG, Miura I, Nakanishi K. Nasute termite soldier frontal gland secretions. 2. Structures of trinervitene congeners from Trinervitermes soldiers [19] Journal of the American Chemical Society. 98: 6062-6064. PMID 965640 DOI: 10.1021/Ja00435A061 |
0.516 |
|
1976 |
Prestwich GD, Tanis SP, Springer JP, Clardy J. NASUTE TERMITE SOLDIER FRONTAL GLAND SECRETIONS. 1. STRUCTURE OF TRINERVI-2β,3α,9α-TRIOL 9-O-ACETATE, A NOVEL DITERPENE FROM TRINERVITERMES SOLDIERS Cheminform. 7. DOI: 10.1002/Chin.197650069 |
0.321 |
|
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