Year |
Citation |
Score |
2016 |
Wang Y, Wach JY, Sheehan P, Zhong C, Zhan C, Harris R, Almo SC, Bishop J, Haggarty SJ, Ramek A, Berry KN, O'Herin C, Koehler AN, Hung AW, Young DW. Diversity-Oriented Synthesis as a Strategy for Fragment Evolution against GSK3β. Acs Medicinal Chemistry Letters. 7: 852-6. PMID 27660690 DOI: 10.1021/Acsmedchemlett.6B00230 |
0.704 |
|
2013 |
Yuan Y, Hartland K, Boskovic Z, Wang Y, Walpita D, Lysy PA, Zhong C, Young DW, Kim YK, Tolliday NJ, Sokal EM, Schreiber SL, Wagner BK. A small-molecule inducer of PDX1 expression identified by high-throughput screening. Chemistry & Biology. 20: 1513-22. PMID 24290880 DOI: 10.1016/J.Chembiol.2013.10.013 |
0.628 |
|
2013 |
Wang Y, Jimenez M, Sheehan P, Zhong C, Hung AW, Tam CP, Young DW. Selective access to trisubstituted macrocyclic E- and Z-alkenes from the ring-closing metathesis of vinylsiloxanes. Organic Letters. 15: 1218-21. PMID 23448432 DOI: 10.1021/Ol400134D |
0.584 |
|
2013 |
Zhong C, Wang Y, O'Herin C, Young DW. Synthesis of substituted morpholines using stereodivergent aza-michael reactions catalyzed by Brønsted acids Acs Catalysis. 3: 643-646. DOI: 10.1021/Cs400031P |
0.591 |
|
2013 |
Comins DL, Higuchi K, Young DW. Dihydropyridine preparation and application in the synthesis of pyridine derivatives Advances in Heterocyclic Chemistry. 110: 175-235. DOI: 10.1016/B978-0-12-408100-0.00006-9 |
0.512 |
|
2011 |
Zhong C, Wang Y, Hung AW, Schreiber SL, Young DW. Diastereoselective control of intramolecular aza-Michael reactions using achiral catalysts. Organic Letters. 13: 5556-9. PMID 21916463 DOI: 10.1021/Ol202276H |
0.634 |
|
2011 |
Pandya BA, Dandapani S, Duvall JR, Rowley A, Mulrooney CA, Ryba T, Dombrowski M, Harton M, Young DW, Marcaurelle LA. Practical asymmetric synthesis of β-hydroxy γ-amino acids via complimentary aldol reactions. Tetrahedron. 67: 6131-6137. PMID 21822337 DOI: 10.1016/J.Tet.2011.06.043 |
0.34 |
|
2011 |
Wang Y, Jimenez M, Hansen AS, Raiber EA, Schreiber SL, Young DW. Control of olefin geometry in macrocyclic ring-closing metathesis using a removable silyl group. Journal of the American Chemical Society. 133: 9196-9. PMID 21557625 DOI: 10.1021/Ja202012S |
0.633 |
|
2011 |
Hung AW, Ramek A, Wang Y, Kaya T, Wilson JA, Clemons PA, Young DW. Route to three-dimensional fragments using diversity-oriented synthesis. Proceedings of the National Academy of Sciences of the United States of America. 108: 6799-804. PMID 21482811 DOI: 10.1073/Pnas.1015271108 |
0.685 |
|
2010 |
Marcaurelle LA, Comer E, Dandapani S, Duvall JR, Gerard B, Kesavan S, Lee MD, Liu H, Lowe JT, Marie JC, Mulrooney CA, Pandya BA, Rowley A, Ryba TD, Suh BC, ... ... Young DW, et al. An aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: discovery of macrocyclic histone deacetylase inhibitors. Journal of the American Chemical Society. 132: 16962-76. PMID 21067169 DOI: 10.1021/Ja105119R |
0.601 |
|
2010 |
Dancík V, Seiler KP, Young DW, Schreiber SL, Clemons PA. Distinct biological network properties between the targets of natural products and disease genes. Journal of the American Chemical Society. 132: 9259-61. PMID 20565092 DOI: 10.1021/Ja102798T |
0.6 |
|
2010 |
Young DW. Synthetic chemistry: An upfront investment. Nature Chemical Biology. 6: 174-175. PMID 20154664 DOI: 10.1038/Nchembio.325 |
0.341 |
|
2009 |
Kelly AR, Wei J, Kesavan S, Marié JC, Windmon N, Young DW, Marcaurelle LA. Accessing skeletal diversity using catalyst control: formation of n and n + 1 macrocyclic triazole rings. Organic Letters. 11: 2257-60. PMID 19473044 DOI: 10.1021/Ol900562U |
0.321 |
|
2007 |
Bender A, Young DW, Jenkins JL, Serrano M, Mikhailov D, Clemons PA, Davies JW. Chemogenomic data analysis: prediction of small-molecule targets and the advent of biological fingerprint. Combinatorial Chemistry & High Throughput Screening. 10: 719-31. PMID 18045083 DOI: 10.2174/138620707782507313 |
0.556 |
|
2005 |
Young DW, Comins DL. Tandem directed lithiations of N-Boc-1,2-dihydropyridines toward highly functionalized 2,3-dihydro-4-pyridones. Organic Letters. 7: 5661-4. PMID 16321016 DOI: 10.1021/Ol052313A |
0.538 |
|
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