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Edward B. Holson - Publications

Affiliations: 
2003 University of Michigan, Ann Arbor, Ann Arbor, MI 
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6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2013 Frumm SM, Fan ZP, Ross KN, Duvall JR, Gupta S, VerPlank L, Suh BC, Holson E, Wagner FF, Smith WB, Paranal RM, Bassil CF, Qi J, Roti G, Kung AL, et al. Selective HDAC1/HDAC2 inhibitors induce neuroblastoma differentiation. Chemistry & Biology. 20: 713-25. PMID 23706636 DOI: 10.1016/J.Chembiol.2013.03.020  0.335
2003 Heo JN, Holson EB, Roush WR. Common-intermediate strategy for synthesis of conduritols and inositols via beta-hydroxy cyclohexenylsilanes. Organic Letters. 5: 1697-700. PMID 12735755 DOI: 10.1021/Ol034349D  0.505
2002 Holson EB, Roush WR. Synthesis of the C(2)-C(13) fragment (the A-B spiroketal unit) of spongistatin 1 (altohyrtin A): use of a common intermediate for the synthesis of both spongistatin spiroketals. Organic Letters. 4: 3723-5. PMID 12375928 DOI: 10.1021/Ol026688X  0.533
2002 Holson EB, Roush WR. Diastereoselective synthesis of the C(17)-C(28) fragment (the C-D spiroketal unit) of spongistatin 1 (altohyrtin A) via a kinetically controlled iodo-spiroketalization reaction. Organic Letters. 4: 3719-22. PMID 12375927 DOI: 10.1021/Ol0266875  0.544
2002 Holson EB, Roush WR. Diastereoselective synthesis of the C(17)-C(28) fragment (the C-D spiroketal unit) of spongistatin 1 (altohyrtin A) via a kinetically controlled lodo-spiroketalization reaction Organic Letters. 4: 3719-3722. DOI: 10.1021/ol0266875  0.517
2002 Johns BA, Grant CM, Marshall JA, Holson EB, Roush WR. Synthesis and utilization of indium (i) iodide for in situ formation of enantioenriched allenylindium reagents and their addition to aldehydes: (2r,3s,4s)-1-(tertbutyldiphenylsilyloxy)-2,4-dimethyl-5-hexyn-3-ol Organic Syntheses. 79: 59-70. DOI: 10.1002/0471264180.Os079.08  0.381
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