Year |
Citation |
Score |
2017 |
Turkyilmaz S, Wilcox CS. Asymmetric solution-phase mixture aldol reaction using oligomeric ethylene glycol tagged chiral oxazolidinones. Tetrahedron Letters. 58: 2031-2033. PMID 29056780 DOI: 10.1016/J.Tetlet.2017.04.026 |
0.768 |
|
2010 |
Pan X, Wilcox CS. Synthesis of dibenzazepinones by palladium-catalyzed intramolecular arylation of o-(2'-bromophenyl)anilide enolates. The Journal of Organic Chemistry. 75: 6445-51. PMID 20822116 DOI: 10.1021/Jo101137R |
0.43 |
|
2010 |
Scott CN, Wilcox CS. A mild synthesis of unsymmetrical bisalkoxysilanes through catalyzed alcoholysis of hydridosilanes containing C-C multiple bonds and aryl halides. The Journal of Organic Chemistry. 75: 253-6. PMID 19954142 DOI: 10.1021/Jo9022765 |
0.42 |
|
2007 |
Bhayana B, Wilcox CS. A minimal protein folding model to measure hydrophobic and CH-pi effects on interactions between nonpolar surfaces in water. Angewandte Chemie (International Ed. in English). 46: 6833-6. PMID 17676565 DOI: 10.1002/Anie.200700932 |
0.629 |
|
2006 |
Curran DP, Zhang Q, Richard C, Lu H, Gudipati V, Wilcox CS. Total synthesis of a 28-member stereoisomer library of murisolins. Journal of the American Chemical Society. 128: 9561-73. PMID 16848495 DOI: 10.1021/Ja061801Q |
0.309 |
|
2006 |
Gudipati V, Curran DP, Wilcox CS. Solution-phase parallel synthesis with oligoethylene glycol sorting tags. Preparation of all four stereoisomers of the hydroxybutenolide fragment of murisolin and related acetogenins. The Journal of Organic Chemistry. 71: 3599-607. PMID 16626147 DOI: 10.1021/Jo060217X |
0.394 |
|
2005 |
Wilcox CS, Gudipati V, Lu H, Turkyilmaz S, Curran DP. Solution-phase mixture synthesis with double-separation tagging: double demixing of a single mixture provides a stereoisomer library of 16 individual murisolins. Angewandte Chemie (International Ed. in English). 44: 6938-40. PMID 16206309 DOI: 10.1002/Anie.200501989 |
0.745 |
|
2005 |
Wilcox CS, Turkyilmaz S. Oligomeric ethylene glycols as sorting tags for parallel and combinatorial mixture synthesis Tetrahedron Letters. 46: 1827-1829. DOI: 10.1016/J.Tetlet.2005.01.109 |
0.733 |
|
2005 |
Scott CN, Wilcox CS. A Mild Synthesis of Unsymmetrical Bis-Alkoxysilanes Through Catalyzed Alcoholysis of Hydridosilanes. Cheminform. 36. DOI: 10.1002/chin.200507168 |
0.327 |
|
2004 |
Bosanac T, Wilcox CS. Precipiton reagents: precipiton phosphines for solution-phase reductions. Organic Letters. 6: 2321-4. PMID 15228269 DOI: 10.1021/ol049369+ |
0.707 |
|
2004 |
Wilcox CS, Scott CN. A Mild Synthesis of Unsymmetrical Bis-Alkoxysilanes through Catalyzed Alcoholysis of Hydridosilanes Synthesis. 2004: 2273-2276. DOI: 10.1055/S-2004-831182 |
0.443 |
|
2003 |
Honigfort ME, Liou S, Rademacher J, Malaba D, Bosanac T, Wilcox CS, Brittain WJ. Copper removal in atom transfer radical polymerization Acs Symposium Series. 854: 250-266. |
0.671 |
|
2002 |
Bosanac T, Wilcox CS. A photoactivated precipiton for reagent sequestration in solution-phase synthesis. Journal of the American Chemical Society. 124: 4194-5. PMID 11960432 DOI: 10.1021/Ja017577G |
0.715 |
|
2002 |
Dixon RW, Radmer RJ, Kuhn B, Kollman PA, Yang J, Raposo C, Wilcox CS, Klumb LA, Stayton PS, Behnke C, Le Trong I, Stenkamp R. Theoretical and experimental studies of biotin analogues that bind almost as tightly to streptavidin as biotin. The Journal of Organic Chemistry. 67: 1827-37. PMID 11895399 DOI: 10.1021/Jo991846S |
0.512 |
|
2002 |
Honigfort ME, Brittain WJ, Bosanac T, Wilcox CS. Use of precipitons for copper removal in atom transfer radical polymerization [1] Macromolecules. 35: 4849-4851. DOI: 10.1021/Ma020155M |
0.67 |
|
2001 |
Bosanac T, Wilcox CS. A novel precipitating auxiliary approach to the purification of Baylis-Hillman adducts. Chemical Communications (Cambridge, England). 1618-9. PMID 12240410 DOI: 10.1039/B103969P |
0.663 |
|
2001 |
Bosanac T, Yang J, Wilcox CS. Precipitons-Functional Protecting Groups to Facilitate Product Separation: Applications in Isoxazoline Synthesis. Angewandte Chemie (International Ed. in English). 40: 1875-1879. PMID 11385660 DOI: 10.1002/1521-3773(20010518)40:10<1875::Aid-Anie1875>3.0.Co;2-5 |
0.739 |
|
2001 |
Bosanac T, Yang J, Wilcox CS. Cover Picture. Angewandte Chemie (International Ed. in English). 40: 1791. PMID 11385650 DOI: 10.1002/1521-3773(20010518)40:10<1791::AID-ANIE1791>3.0.CO;2-V |
0.75 |
|
2001 |
Bosanac T, Wilcox CS. Precipiton strategies applied to the isolation of α-substituted β-ketoesters Tetrahedron Letters. 42: 4309-4312. DOI: 10.1016/S0040-4039(01)00726-2 |
0.711 |
|
1992 |
Nagai M, Gaudino JJ, Wilcox CS. Acyclic Stereocontrol in Additions of Grignard Reagents to α-Alkoxyiminium Ions. A Stereoselective Approach tothreoAmino Ethers Synthesis. 1992: 163-168. DOI: 10.1055/S-1992-34180 |
0.305 |
|
1990 |
Gaudino JJ, Wilcox CS. A general approach to carbocyclic sugar analogs: preparation of a carbocyclic analog of β-d-fructofuranose☆☆☆ Carbohydrate Research. 206: 233-250. PMID 2073635 DOI: 10.1016/0008-6215(90)80063-9 |
0.309 |
|
1986 |
WILCOX CS, BABSTON RE. ChemInform Abstract: Convenient Synthesis of Ethyl Triethylsilyldiazoacetate and Stereoselective Preparation of Aliphatic Silylketene Acetals: In situ Formation of Triethylsilyl Perchlorate. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198608225 |
0.34 |
|
1985 |
Wilcox CS, Babston RE. Convenient Synthesis of Ethyl Triethylsilyldiazoacetate and Stereoselective Preparation of Aliphatic Silylketene Acetals:In situFormation of Triethylsilyl Perchlorate Synthesis. 1985: 941-943. DOI: 10.1055/s-1985-31393 |
0.352 |
|
1984 |
Wilcox CS, Babston RE. Thermodynamic results for geometrical isomerism in silyl ketene acetals The Journal of Organic Chemistry. 49: 1451-1453. DOI: 10.1021/Jo00182A031 |
0.368 |
|
1983 |
Ireland RE, Anderson RC, Badoud R, Fitzsimmons BJ, McGarvey GJ, Thaisrivongs S, Wilcox CS. The total synthesis of ionophore antibiotics. A convergent synthesis of lasalocid A (X537A) Journal of the American Chemical Society. 105: 1988-2006. DOI: 10.1021/Ja00345A055 |
0.546 |
|
1983 |
IRELAND RE, ANDERSON RC, BADOUD R, FITZSIMMONS BJ, MCGARVEY GJ, THAISRIVONGS S, WILCOX CS. ChemInform Abstract: THE TOTAL SYNTHESIS OF IONOPHORE ANTIBIOTICS. A CONVERGENT SYNTHESIS OF LASALOCID A (X537A) Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198328370 |
0.555 |
|
1980 |
Ireland RE, Wilcox CS. New and efficient synthesis of 6-deoxy-L-gulose Journal of Organic Chemistry. 45: 197-203. DOI: 10.1021/Jo01290A001 |
0.55 |
|
1980 |
Ireland RE, Thaisrivongs S, Vanier N, Wilcox CS. Enolate Claisen rearrangement of esters from furanoid and pyranoid glycals Journal of Organic Chemistry. 45: 48-61. DOI: 10.1021/Jo01289A012 |
0.542 |
|
1980 |
Ireland RE, Thaisrivongs S, Wilcox CS. Total synthesis of lasalocid A (X537A) Journal of the American Chemical Society. 102: 1155-1157. DOI: 10.1021/Ja00523A038 |
0.551 |
|
1980 |
Wilcox C, Breslow R. A convenient synthesis of bis-dialkylaminoacetylenes Tetrahedron Letters. 21: 3241-3242. DOI: 10.1016/S0040-4039(00)78656-4 |
0.424 |
|
1980 |
WILCOX C, BRESLOW R. ChemInform Abstract: A CONVENIENT SYNTHESIS OF BIS(DIALKYLAMINO)ACETYLENES Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198047143 |
0.524 |
|
1980 |
IRELAND RE, THAISRIVONGS S, VANIER N, WILCOX CS. ChemInform Abstract: ENOLATE CLAISEN REARRANGEMENT OF ESTERS FROM FURANOID AND PYRANOID GLYCALS Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198023119 |
0.537 |
|
1980 |
IRELAND RE, THAISRIVONGS S, WILCOX CS. ChemInform Abstract: TOTAL SYNTHESIS OF LASALOCID A (X537A) Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198019316 |
0.561 |
|
1979 |
Ireland RE, Wilcox CS, Thaisrivongs S, Vanier NR. The generation of C-glycosides through the enolate Claisen rearrangement Canadian Journal of Chemistry. 57: 1743-1745. DOI: 10.1139/V79-278 |
0.545 |
|
1978 |
Ireland RE, Wilcox CS, Thaisrivongs S. An efficient method for the preparation of furanoid and pyranoid glycals Journal of Organic Chemistry. 43: 786-787. DOI: 10.1021/Jo00398A078 |
0.548 |
|
1978 |
IRELAND RE, WILCOX CS, THAISRIVONGS S. ChemInform Abstract: AN EFFICIENT METHOD FOR THE PREPARATION OF FURANOID AND PYRANOID GLYCALS Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197827216 |
0.52 |
|
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