Year |
Citation |
Score |
2019 |
Bennett R, Biba M, Liu J, Haidar Ahmad IA, Hicks MB, Regalado EL. Enhanced fluidity liquid chromatography: A guide to scaling up from analytical to preparative separations. Journal of Chromatography. A. PMID 30803788 DOI: 10.1016/J.Chroma.2019.02.017 |
0.396 |
|
2016 |
Zawatzky K, Biba M, Regalado EL, Welch CJ. MISER chiral supercritical fluid chromatography for high throughput analysis of enantiopurity. Journal of Chromatography. A. 1429: 374-9. PMID 26747691 DOI: 10.1016/J.Chroma.2015.12.057 |
0.336 |
|
2014 |
Biba M, Regalado EL, Wu N, Welch CJ. Effect of particle size on the speed and resolution of chiral separations using supercritical fluid chromatography. Journal of Chromatography. A. 1363: 250-6. PMID 25082525 DOI: 10.1016/J.Chroma.2014.07.010 |
0.419 |
|
2014 |
Biba M, Welch CJ, Foley JP. Investigation of a new core-shell particle column for ion-pair reversed-phase liquid chromatography analysis of oligonucleotides. Journal of Pharmaceutical and Biomedical Analysis. 96: 54-7. PMID 24727281 DOI: 10.1016/J.Jpba.2014.03.029 |
0.585 |
|
2013 |
Schafer W, Chandrasekaran T, Pirzada Z, Zhang C, Gong X, Biba M, Regalado EL, Welch CJ. Improved chiral SFC screening for analytical method development. Chirality. 25: 799-804. PMID 23946148 DOI: 10.1002/Chir.22218 |
0.433 |
|
2013 |
Biba M, Jiang E, Mao B, Zewge D, Foley JP, Welch CJ. Factors influencing the separation of oligonucleotides using reversed-phase/ion-exchange mixed-mode high performance liquid chromatography columns. Journal of Chromatography. A. 1304: 69-77. PMID 23859796 DOI: 10.1016/J.Chroma.2013.06.050 |
0.567 |
|
2013 |
Biba M, Welch CJ, Foley JP, Mao B, Vazquez E, Arvary RA. Evaluation of core-shell particle columns for ion-pair reversed-phase liquid chromatography analysis of oligonucleotides. Journal of Pharmaceutical and Biomedical Analysis. 72: 25-32. PMID 23146223 DOI: 10.1016/J.Jpba.2012.09.007 |
0.58 |
|
2011 |
Gong X, Craven T, Schafer W, Pirzada Z, Biba M, Welch CJ. Estimating chromatographic enantioselectivity (α) from gradient enantioselective chromatography data. Chirality. 23: 128-32. PMID 20803492 DOI: 10.1002/Chir.20887 |
0.341 |
|
2010 |
Pirzada Z, Personick M, Biba M, Gong X, Zhou L, Schafer W, Roussel C, Welch CJ. Systematic evaluation of new chiral stationary phases for supercritical fluid chromatography using a standard racemate library. Journal of Chromatography. A. 1217: 1134-8. PMID 19850298 DOI: 10.1016/J.Chroma.2009.10.004 |
0.4 |
|
2010 |
Zhou L, Antonucci V, Biba M, Gong X, Ge Z. Simultaneous enantioseparation of a basic active pharmaceutical ingredient compound and its neutral intermediate using reversed phase and normal phase liquid chromatography with a new type of polysaccharide stationary phase. Journal of Pharmaceutical and Biomedical Analysis. 51: 153-7. PMID 19766423 DOI: 10.1016/J.Jpba.2009.08.027 |
0.433 |
|
2010 |
Welch CJ, Wu N, Biba M, Hartman R, Brkovic T, Gong X, Helmy R, Schafer W, Cuff J, Pirzada Z, Zhou L. Greening analytical chromatography Trac - Trends in Analytical Chemistry. 29: 667-680. DOI: 10.1016/J.Trac.2010.03.008 |
0.377 |
|
2009 |
Welch CJ, Gong X, Schafer W, Chobanian H, Lin L, Biba M, Liu P, Guo Y, Beard A. Factors influencing the interconversion of a new class of dibenzodiazepine sulfonamide atropisomers. Chirality. 21: E105-9. PMID 19885821 DOI: 10.1002/Chir.20785 |
0.301 |
|
2008 |
Welch CJ, Biba M, Pye P, Angelaud R, Egbertson M. Serendipitous discovery of a pH-dependant atropisomer bond rotation: toward a write-protectable chiral molecular switch? Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences. 875: 118-21. PMID 18819851 DOI: 10.1016/J.Jchromb.2008.08.028 |
0.326 |
|
2007 |
Helmy R, Biba M, Zang J, Mao B, Fogelman K, Vlachos V, Hosek P, Welch CJ. Improving sensitivity in chiral supercritical fluid chromatography for analysis of active pharmaceutical ingredients. Chirality. 19: 787-92. PMID 17722016 DOI: 10.1002/Chir.20451 |
0.314 |
|
2007 |
Leonard WR, Henderson DW, Miller RA, Spencer GA, Sudah OS, Biba M, Welch CJ. Strategic use of preparative chiral chromatography for the synthesis of a preclinical pharmaceutical candidate. Chirality. 19: 693-700. PMID 17354260 DOI: 10.1002/Chir.20378 |
0.414 |
|
2007 |
Welch CJ, Biba M, Gouker JR, Kath G, Augustine P, Hosek P. Solving multicomponent chiral separation challenges using a new SFC tandem column screening tool. Chirality. 19: 184-9. PMID 17192838 DOI: 10.1002/Chir.20357 |
0.405 |
|
2007 |
Welch CJ, Biba M, Sajonz P. Fast methods of enantiopurity determination for the Soai reaction: towards a general enantioenrichment detector? Chirality. 19: 34-43. PMID 17089338 DOI: 10.1002/Chir.20336 |
0.343 |
|
2006 |
Sajonz P, Gong X, Leonard WR, Biba M, Welch CJ. Multiparallel chiral method development screening using an 8-channel microfluidic HPLC system. Chirality. 18: 803-13. PMID 16906503 DOI: 10.1002/Chir.20325 |
0.376 |
|
2005 |
Shafiee A, Upadhyay V, Corley EG, Biba M, Zhao D, Marcoux JF, Campos KR, Journet M, King AO, Larsen RD, Grabowski EJJ, Volante RP, Tillyer RD. An efficient enzyme-catalyzed kinetic resolution: Large-scale preparation of an enantiomerically pure indole-ethyl ester derivative, a key component for the synthesis of a prostaglandin D2 receptor antagonist, an anti-allergic rhinitis drug candidate Tetrahedron Asymmetry. 16: 3094-3098. DOI: 10.1016/J.Tetasy.2005.08.021 |
0.325 |
|
2003 |
Welch CJ, Biba M, Drahus A, Conlon DA, Tung HH, Collins P. Selective removal of a pharmaceutical process impurity using a reactive resin Journal of Liquid Chromatography and Related Technologies. 26: 1959-1968. DOI: 10.1081/Jlc-120021763 |
0.306 |
|
2002 |
Welch CJ, Shaimi M, Biba M, Chilenski JR, Szumigala RH, Dolling U, Mathre DJ, Reider PJ. Microplate evaluation of process adsorbents Journal of Separation Science. 25: 847-850. DOI: 10.1002/1615-9314(20020901)25:13<847::Aid-Jssc847>3.0.Co;2-2 |
0.316 |
|
2001 |
Solladié-Cavallo A, Sedy O, Salisova M, Biba M, Welch CJ, Nafié L, Freedman T. A chiral 1,4-oxazin-2-one: Asymmetric synthesis versus resolution, structure, conformation and VCD absolute configuration Tetrahedron Asymmetry. 12: 2703-2707. DOI: 10.1016/S0957-4166(01)00478-5 |
0.334 |
|
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