Year |
Citation |
Score |
2013 |
Dandepally SR, Elgoummadi R, Williams AL. Schwartz reagent mediated synthesis of thiazolones and imidazolones from thiazolidine-2,4-diones and imidazolidine-2,4-diones Tetrahedron Letters. 54: 925-928. DOI: 10.1016/j.tetlet.2012.12.015 |
0.349 |
|
2012 |
Williams AL, St Hilaire VR, Lee T. Regioselective reduction of 3-substituted N-acylpyrazinium salts toward the synthesis of 1,2-dihydropyrazines. The Journal of Organic Chemistry. 77: 4097-102. PMID 22404580 DOI: 10.1021/jo202498r |
0.471 |
|
2011 |
Srinivasan JM, Mathew PA, Williams AL, Huffman JC, Johnston JN. Stereoselective synthesis of complex polycyclic aziridines: use of the Brønsted acid-catalyzed aza-Darzens reaction to prepare an orthogonally protected mitomycin C intermediate with maximal convergency. Chemical Communications (Cambridge, England). 47: 3975-7. PMID 21347494 DOI: 10.1039/C0Cc05734G |
0.699 |
|
2010 |
Williams AL, Dandepally SR, Gilyazova N, Witherspoon SM, Ibeanu G. Microwave-assisted synthesis of 4-chloro-N-(naphthalen-1-ylmethyl)-5-(3-(piperazin-1-yl)phenoxy)thiophene-2-sulfonamide (B-355252): a new potentiator of Nerve Growth Factor (NGF)-induced neurite outgrowth. Tetrahedron. 66: 9577-9581. PMID 22973068 DOI: 10.1016/j.tet.2010.09.028 |
0.331 |
|
2010 |
Williams AL, Dandepally SR, Kotturi SV. A p-methoxybenzyl (PMB) protection/deprotection approach toward the synthesis of 5-phenoxy-4-chloro-N-(aryl/alkyl) thiophene-2-sulfonamides. Molecular Diversity. 14: 697-707. PMID 19936959 DOI: 10.1007/s11030-009-9208-y |
0.456 |
|
2006 |
Williams AL, Srinivasan JM, Johnston JN. Synthesis of an advanced intermediate en route to the mitomycin natural products. Organic Letters. 8: 6047-9. PMID 17165926 DOI: 10.1021/Ol0624676 |
0.692 |
|
2004 |
Williams AL, Johnston JN. The Brønsted acid-catalyzed direct aza-Darzens synthesis of N-alkyl cis-aziridines. Journal of the American Chemical Society. 126: 1612-3. PMID 14871074 DOI: 10.1021/Ja0385282 |
0.606 |
|
2003 |
Nugent BM, Williams AL, Prabhakaran EN, Johnston JN. Free radical-mediated vinyl amination: A mild, general pyrrolidinyl enamine synthesis Tetrahedron. 59: 8877-8888. DOI: 10.1016/J.Tet.2003.04.003 |
0.667 |
|
2003 |
Prabhakaran EN, Nugent BM, Williams AL, Nailor KE, Johnston JN. Free Radical Mediated Vinyl Amination: Access-to N,N-Dialkyl Enamines and Their β-Stannyl and β-Thio Derivatives. Cheminform. 34. DOI: 10.1002/chin.200315118 |
0.698 |
|
2002 |
Prabhakaran EN, Nugent BM, Williams AL, Nailor KE, Johnston JN. Free radical-mediated vinyl amination: access to N,N-dialkyl enamines and their beta-stannyl and beta-thio derivatives. Organic Letters. 4: 4197-200. PMID 12443057 DOI: 10.1021/Ol027064U |
0.668 |
|
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