Year |
Citation |
Score |
2017 |
Wegener A, Miller KA. Total Synthesis of Avrainvilleol. The Journal of Organic Chemistry. PMID 28982008 DOI: 10.1021/Acs.Joc.7B02028 |
0.381 |
|
2013 |
Mancha SR, Regnery CM, Dahlke JR, Miller KA, Blake DJ. Antiviral activity of (+)-sattabacin against varicella zoster. Bioorganic & Medicinal Chemistry Letters. 23: 562-4. PMID 23219702 DOI: 10.1016/J.Bmcl.2012.11.017 |
0.314 |
|
2013 |
Snyder KM, Doty TS, Heins SP, Desouchet AL, Miller KA. Asymmetric total synthesis of (+)-sattazolin Tetrahedron Letters. 54: 192-194. DOI: 10.1016/J.Tetlet.2012.10.124 |
0.396 |
|
2011 |
Chen Z, Forman LW, Miller KA, English B, Takashima A, Bohacek RA, Williams RM, Faller DV. Protein kinase Cδ inactivation inhibits cellular proliferation and decreases survival in human neuroendocrine tumors. Endocrine-Related Cancer. 18: 759-71. PMID 21990324 DOI: 10.1530/Erc-10-0224 |
0.444 |
|
2010 |
Ding Y, de Wet JR, Cavalcoli J, Li S, Greshock TJ, Miller KA, Finefield JM, Sunderhaus JD, McAfoos TJ, Tsukamoto S, Williams RM, Sherman DH. Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp. Journal of the American Chemical Society. 132: 12733-40. PMID 20722388 DOI: 10.1021/Ja1049302 |
0.678 |
|
2010 |
Aronoff MR, Bourjaily NA, Miller KA. Concise, protecting group free total syntheses of (+)-sattabacin and (+)-4-hydroxysattabacin Tetrahedron Letters. 51: 6375-6377. DOI: 10.1016/J.Tetlet.2010.09.147 |
0.724 |
|
2009 |
Miller KA, Tsukamoto S, Williams RM. Asymmetric total syntheses of (+)- and (-)-versicolamide B and biosynthetic implications. Nature Chemistry. 1: 63-8. PMID 20300443 DOI: 10.1038/Nchem.110 |
0.543 |
|
2009 |
Miller KA, Williams RM. Synthetic approaches to the bicyclo[2.2.2]diazaoctane ring system common to the paraherquamides, stephacidins and related prenylated indole alkaloids. Chemical Society Reviews. 38: 3160-74. PMID 19847349 DOI: 10.1039/B816705M |
0.547 |
|
2009 |
Li Z, Hu M, Leung C, Steinberg JA, Shen J, Li M, Wang CS, Sanchez E, Bowers A, Greshock T, Miller K, Newkirk T, West N, Bradner JE, Williams RM, et al. Largazole, a Novel Cyclic Peptide Histone Deacetylase Inhibitor, Demonstrates Anti-MM Effects Alone and Increases the Anti-MM Effects of Bortezomib. Blood. 114: 4925-4925. DOI: 10.1182/Blood.V114.22.4925.4925 |
0.59 |
|
2009 |
Cao H, Fei RG, Bowers AA, Greshock TJ, Newkirt T, Miller KA, Bradner JE, West N, Williams RM, Papayannopoulou T, Stamatoyannopoulos G. Potent Induction of Human γ Globin Gene Expression by Largazole, a New Histone Deacetylase Inhibitor. Blood. 114: 2022-2022. DOI: 10.1182/Blood.V114.22.2022.2022 |
0.655 |
|
2009 |
Miller KA, Tsukamoto S, Williams RM. Erratum: Asymmetric total syntheses of (+)- and (−)-versicolamide B and biosynthetic implications Nature Chemistry. 1: 165-165. DOI: 10.1038/Nchem.195 |
0.432 |
|
2008 |
Miller KA, Shanahan CS, Martin SF. The Pauson-Khand Reaction as a New Entry to the Synthesis of Bridged Bicyclic Heterocycles: Application to the Enantioselective Total Synthesis of (-)-Alstonerine. Tetrahedron. 64: 6884-6900. PMID 19122869 DOI: 10.1016/J.Tet.2008.02.066 |
0.544 |
|
2008 |
Miller KA, Figueroa M, Valente MW, Greshock TJ, Mata R, Williams RM. Calmodulin inhibitory activity of the malbrancheamides and various analogs. Bioorganic & Medicinal Chemistry Letters. 18: 6479-81. PMID 18986806 DOI: 10.1016/J.Bmcl.2008.10.057 |
0.486 |
|
2008 |
Ding Y, Greshock TJ, Miller KA, Sherman DH, Williams RM. Premalbrancheamide: synthesis, isotopic labeling, biosynthetic incorporation, and detection in cultures of Malbranchea aurantiaca. Organic Letters. 10: 4863-6. PMID 18844365 DOI: 10.1021/Ol8019633 |
0.386 |
|
2008 |
Miller KA, Welch TR, Greshock TJ, Ding Y, Sherman DH, Williams RM. Biomimetic total synthesis of malbrancheamide and malbrancheamide B. The Journal of Organic Chemistry. 73: 3116-9. PMID 18345688 DOI: 10.1021/Jo800116Y |
0.65 |
|
2007 |
Ashfeld BL, Miller KA, Smith AJ, Tran K, Martin SF. Features and applications of [Rh(CO)(2)Cl](2)-catalyzed alkylations of unsymmetrical allylic substrates. The Journal of Organic Chemistry. 72: 9018-31. PMID 17973524 DOI: 10.1021/Jo701290B |
0.708 |
|
2007 |
Miller KA, Martin SF. Concise, enantioselective total synthesis of (-)-alstonerine. Organic Letters. 9: 1113-6. PMID 17298078 DOI: 10.1021/Ol0700761 |
0.538 |
|
2007 |
Miller KA, Shanahan CS, Martin SF. Synthesis of (-)-Alstonerine Synfacts. 2007: 785-785. DOI: 10.1055/S-0028-1083565 |
0.493 |
|
2005 |
Ashfeld BL, Miller KA, Smith AJ, Tran K, Martin SF. [Rh(CO)2Cl]2-catalyzed domino reactions involving allylic substitution and subsequent carbocyclization reactions. Organic Letters. 7: 1661-3. PMID 15816777 DOI: 10.1021/Ol0504300 |
0.685 |
|
2004 |
Ashfeld BL, Miller KA, Martin SF. Direct, stereoselective substitution in [Rh(CO)(2)Cl](2)-catalyzed allylic alkylations of unsymmetrical substrates. Organic Letters. 6: 1321-4. PMID 15070327 DOI: 10.1021/Ol0496529 |
0.684 |
|
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