Year |
Citation |
Score |
2020 |
Zhang X, Smith RT, Le C, McCarver SJ, Shireman BT, Carruthers NI, MacMillan DWC. Copper-mediated synthesis of drug-like bicyclopentanes. Nature. PMID 32066140 DOI: 10.1038/S41586-020-2060-Z |
0.311 |
|
2010 |
Graham JM, Shireman BT, Maddux TM, Brandstedt CM, Zeller WE. ChemInform Abstract: DIC-Mediated Coupling of Carboxylic Acids to (4R,5S)-4-Methyl-5-phenyl-2-oxazolidinone. Cheminform. 31: no-no. DOI: 10.1002/chin.200033122 |
0.398 |
|
2005 |
Trost BM, Frederiksen MU, Papillon JP, Harrington PE, Shin S, Shireman BT. Dinuclear asymmetric Zn aldol additions: formal asymmetric synthesis of fostriecin. Journal of the American Chemical Society. 127: 3666-7. PMID 15771479 DOI: 10.1021/Ja042435I |
0.31 |
|
2001 |
Shireman BT, Miller MJ, Jonas M, Wiest O. Conformational study and enantioselective, regiospecific syntheses of novel aminoxy trans-proline analogues derived from an acylnitroso Diels-Alder cycloaddition. The Journal of Organic Chemistry. 66: 6046-56. PMID 11529730 DOI: 10.1021/Jo010284L |
0.513 |
|
2001 |
Shireman BT, Miller MJ. Synthesis of enantiomerically and diastereomerically pure 2(S)-amino-6(R)-hydroxy-1,7-heptanedioic acid dimethyl ester hydrochloride from cycloheptadiene. The Journal of Organic Chemistry. 66: 4809-13. PMID 11442409 DOI: 10.1021/Jo015544D |
0.546 |
|
2001 |
Shireman BT, Miller MJ. ChemInform Abstract: Rapid Syntheses of Either Enantiomer of Important Carbocyclic Nucleoside Precursors. Cheminform. 32: no-no. DOI: 10.1002/chin.200110234 |
0.461 |
|
2000 |
Shireman BT, Miller MJ. Rapid syntheses of either enantiomer of important carbocyclic nucleoside precursors Tetrahedron Letters. 41: 9537-9540. DOI: 10.1016/S0040-4039(00)01668-3 |
0.556 |
|
2000 |
Shireman BT, Miller MJ. Rapid syntheses of either enantiomer of important carbocyclic nucleoside precursors Tetrahedron Letters. 41: 9537-9540. |
0.459 |
|
2000 |
Graham JM, Shireman BT, Maddux TM, Brandstedt CM, Zeller WE. DIC-mediated coupling of carboxylic acids to (4r, 5s)-4-methyl-5-phenyl- 2-oxazolidinone Synthetic Communications. 30: 1221-1226. |
0.378 |
|
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