Brock T. Shireman, Ph.D.

Affiliations: 
2001 University of Notre Dame, Notre Dame, IN, United States 
Area:
chemical and enzymatic synthesis and study of biologically important, heteroatom-containing systems including amino acids, peptides, antibiotics, siderophores, and others
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"Brock Shireman"
Mean distance: 9.27
 

Parents

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Marvin J. Miller grad student 2001 Notre Dame
 (Acylnitroso Diels -Alder cycloadducts: Scaffolds for the syntheses of enantiomerically pure biologically relevant molecules.)
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Publications

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Zhang X, Smith RT, Le C, et al. (2020) Copper-mediated synthesis of drug-like bicyclopentanes. Nature
Graham JM, Shireman BT, Maddux TM, et al. (2010) ChemInform Abstract: DIC-Mediated Coupling of Carboxylic Acids to (4R,5S)-4-Methyl-5-phenyl-2-oxazolidinone. Cheminform. 31: no-no
Trost BM, Frederiksen MU, Papillon JP, et al. (2005) Dinuclear asymmetric Zn aldol additions: formal asymmetric synthesis of fostriecin. Journal of the American Chemical Society. 127: 3666-7
Shireman BT, Miller MJ, Jonas M, et al. (2001) 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
Shireman BT, Miller MJ. (2001) 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
Shireman BT, Miller MJ. (2001) ChemInform Abstract: Rapid Syntheses of Either Enantiomer of Important Carbocyclic Nucleoside Precursors. Cheminform. 32: no-no
Shireman BT, Miller MJ. (2000) Rapid syntheses of either enantiomer of important carbocyclic nucleoside precursors Tetrahedron Letters. 41: 9537-9540
Shireman BT, Miller MJ. (2000) Rapid syntheses of either enantiomer of important carbocyclic nucleoside precursors Tetrahedron Letters. 41: 9537-9540
Graham JM, Shireman BT, Maddux TM, et al. (2000) DIC-mediated coupling of carboxylic acids to (4r, 5s)-4-methyl-5-phenyl- 2-oxazolidinone Synthetic Communications. 30: 1221-1226
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