Brian M. Casey, Ph.D. - Publications
Affiliations: | Lehigh University, Bethlehem, PA, United States |
Year | Citation | Score | |||
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2013 | Casey BM, Sadasivam DV, Flowers Ii RA. Mechanistic studies on the CAN-mediated intramolecular cyclization of δ-aryl-β-dicarbonyl compounds. Beilstein Journal of Organic Chemistry. 9: 1472-9. PMID 23946845 DOI: 10.3762/Bjoc.9.167 | 0.396 | |||
2011 | Casey BM, Flowers RA. On the nature of the oxidative heterocoupling of lithium enolates. Journal of the American Chemical Society. 133: 11492-5. PMID 21721524 DOI: 10.1021/Ja205017E | 0.62 | |||
2010 | Casey BM, Eakin CA, Jiao J, Sadasivam DV, Flowers RA. Corrigendum to Solvent-dependent oxidative coupling of 1-aryl-1,3-dicarbonyls and styrene. Tetrahedron. 66: 5720-5726. PMID 20806051 DOI: 10.1016/J.Tet.2010.05.063 | 0.681 | |||
2010 | Casey BM, Eakin CA, Jiao J, Sadasivam DV, Flowers RA. Corrigendum to ‘Solvent-dependent oxidative coupling of 1-aryl-1,3-dicarbonyls and styrene’ [Tetrahedron 65 (52) (2009) 10762–10768] Tetrahedron. 66: 5719. DOI: 10.1016/J.Tet.2010.05.062 | 0.645 | |||
2010 | Casey BM, Eakin CA, Jiao J, Sadasivam DV, Flowers RAI. ChemInform Abstract: Solvent-Dependent Oxidative Coupling of 1-Aryl-1,3-dicarbonyls and Styrene. Cheminform. 41. DOI: 10.1002/chin.201018033 | 0.657 | |||
2009 | Devery JJ, Mohanta PK, Casey BM, Flowers RA. Facile Route to Tetrasubstituted Pyrazoles Utilizing Ceric Ammonium Nitrate. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 1490-1494. PMID 21151843 DOI: 10.1055/S-0029-1217163 | 0.543 | |||
2009 | Casey BM, Eakin CA, Flowers RA. Synthesis of gamma-halogenated ketones via the Ce(IV)-mediated oxidative coupling of cyclobutanols and inorganic halides. Tetrahedron Letters. 50: 1264-1266. PMID 20676239 DOI: 10.1016/J.Tetlet.2008.12.114 | 0.647 | |||
2009 | Casey BM, Eakin CA, Jiao J, Sadasivam DV, Flowers RA. Solvent-dependent oxidative coupling of 1-aryl-1,3-dicarbonyls and styrene. Tetrahedron. 65: 10762-10768. PMID 20625455 DOI: 10.1016/J.Tet.2009.06.118 | 0.676 | |||
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