Year |
Citation |
Score |
2018 |
Beutner G, Carrasquillo R, Geng P, Hsiao Y, Huang EC, Janey J, Katipally K, Kolotuchin S, La Porte T, Lee A, Lobben P, Lora-Gonzalez F, Mack B, Mudryk B, Qiu Y, ... ... Razler TM, et al. Adventures in Atropisomerism: Total Synthesis of a Complex Active Pharmaceutical Ingredient with Two Chirality Axes. Organic Letters. PMID 29909639 DOI: 10.1021/Acs.Orglett.8B01218 |
0.343 |
|
2017 |
Beutner GL, Hsiao Y, Razler T, Simmons EM, Wertjes W. Nickel-Catalyzed Synthesis of Quinazolinediones. Organic Letters. 19: 1052-1055. PMID 28253632 DOI: 10.1021/Acs.Orglett.7B00052 |
0.307 |
|
2016 |
Conlon DA, Natalie KJ, Cuniere N, Razler TM, Zhu J, De Mas N, Tymonko S, Fraunhoffer KJ, Sortore E, Rosso VW, Xu Z, Adams ML, Patel A, Huang J, Gong H, et al. Development of a Practical Synthesis of Functionalized Azaxanthene-Derived Nonsteroidal Glucocorticoid Receptor Modulators Organic Process Research and Development. 20: 921-933. DOI: 10.1021/Acs.Oprd.6B00035 |
0.349 |
|
2011 |
Smith AB, Hogan AM, Liu Z, Razler TM, Meis RM, Morinaka BI, Molinski TF. Phorboxazole Synthetic Studies: Design, Synthesis and Biological Evaluation of Phorboxazole A and Hemi-Phorboxazole A Related Analogues. Tetrahedron. 67: 5069-5078. PMID 21811346 DOI: 10.1016/J.Tet.2010.12.043 |
0.464 |
|
2011 |
Zhu J, Razler TM, Xu Z, Conlon DA, Sortore EW, Fritz AW, Demerzhan R, Sweeney JT. A robust three-step telescoped synthesis of electron-deficient amide substituted arylboronic acids Organic Process Research and Development. 15: 438-442. DOI: 10.1021/op100267p |
0.331 |
|
2008 |
Smith AB, Fox RJ, Razler TM. Evolution of the Petasis-Ferrier union/rearrangement tactic: construction of architecturally complex natural products possessing the ubiquitous cis-2,6-substituted tetrahydropyran structural element. Accounts of Chemical Research. 41: 675-87. PMID 18489082 DOI: 10.1021/ar700234r |
0.394 |
|
2008 |
Smith AB, Razler TM, Meis RM, Pettit GR. Synthesis and biological evaluation of phorboxazole congeners leading to the discovery and preparative-scale synthesis of (+)-chlorophorboxazole a possessing picomolar human solid tumor cell growth inhibitory activity. The Journal of Organic Chemistry. 73: 1201-8. PMID 18215059 DOI: 10.1021/Jo701816H |
0.366 |
|
2008 |
Smith AB, Razler TM, Ciavarri JP, Hirose T, Ishikawa T, Meis RM. A second-generation total synthesis of (+)-phorboxazole A. The Journal of Organic Chemistry. 73: 1192-200. PMID 18215058 DOI: 10.1021/Jo7018152 |
0.474 |
|
2008 |
Smith, III A, Razler T, Ciavarri J, Hirose T, Ishikawa T, Meis R. Synthesis of (+)-Phorboxazole A Synfacts. 2008: 0671-0671. DOI: 10.1055/S-2008-1077858 |
0.404 |
|
2006 |
Smith AB, Razler TM, Meis RM, Pettit GR. Design and synthesis of a potent phorboxazole C(11-15) acetal analogue. Organic Letters. 8: 797-9. PMID 16468770 DOI: 10.1021/Ol060014V |
0.417 |
|
2005 |
Smith AB, Razler TM, Pettit GR, Chapuis JC. (+)-Phorboxazole A synthetic studies. Identification of a series of highly cytotoxic C(45-46) analogues. Organic Letters. 7: 4403-6. PMID 16178544 DOI: 10.1021/Ol051585A |
0.378 |
|
2005 |
Smith AB, Razler TM, Ciavarri JP, Hirose T, Ishikawa T. (+)-Phorboxazole A synthetic studies. A highly convergent, second generation total synthesis of (+)-phorboxazole A. Organic Letters. 7: 4399-402. PMID 16178543 DOI: 10.1021/Ol051584I |
0.468 |
|
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