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Timothy S. Snowden, Ph.D. - Publications

Affiliations: 
Chemistry The University of Alabama, Tuscaloosa, AL 
Area:
Organic Chemistry, Synthetic Methodology, Natural Product Synthesis
Website:
http://www.bama.ua.edu/~chem/people/faculty/snowden/snowden.html

21/32 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
2020 Gibbons GS, Chakraborty A, Grigsby SM, Umeano AC, Liao C, Moukha-Chafiq O, Pathak V, Mathew B, Lee YT, Dou Y, Schürer SC, Reynolds RC, Snowden TS, Nikolovska-Coleska Z. Identification of DOT1L inhibitors by structure-based virtual screening adapted from a nucleoside-focused library. European Journal of Medicinal Chemistry. 189: 112023. PMID 31978781 DOI: 10.1016/J.Ejmech.2019.112023  0.555
2019 Moukha-Chafiq O, Reynolds RC, Wilson JC, Snowden TS. Parallel Solution Phase Synthesis and Preliminary Biological Activity of a 5'-Substituted Cytidine Analog Library. Acs Combinatorial Science. PMID 31365223 DOI: 10.1021/Acscombsci.9B00072  0.411
2014 Gupta MK, Li Z, Snowden TS. Preparation of one-carbon homologated amides from aldehydes or primary alcohols. Organic Letters. 16: 1602-5. PMID 24593196 DOI: 10.1021/Ol500200N  0.56
2014 Bhattarai BT, Adhikari S, Kimball EA, Moore JN, Shaughnessy KH, Snowden TS, Fronczek FR, Dolliver DD. Palladium-catalyzed ortho-halogenation of diaryl oxime ethers Tetrahedron Letters. 4801-4806. DOI: 10.1016/J.Tetlet.2014.06.080  0.453
2013 Dolliver DD, Bhattarai BT, Pandey A, Lanier ML, Bordelon AS, Adhikari S, Dinser JA, Flowers PF, Wills VS, Schneider CL, Shaughnessy KH, Moore JN, Raders SM, Snowden TS, McKim AS, et al. Stereospecific Suzuki, Sonogashira, and Negishi coupling reactions of N-alkoxyimidoyl iodides and bromides. The Journal of Organic Chemistry. 78: 3676-87. PMID 23534335 DOI: 10.1021/Jo400179U  0.39
2013 Snider JR, Entrekin JT, Snowden TS, Dolliver D. Synthesis of potent CERT inhibitor HPA-12 featuring a tandem corey-link and intramolecular nucleophilic acyl substitution reaction Synthesis (Germany). 45: 1899-1903. DOI: 10.1055/S-0033-1338495  0.456
2012 Gupta MK, Li Z, Snowden TS. One-pot synthesis of trichloromethyl carbinols from primary alcohols. The Journal of Organic Chemistry. 77: 4854-60. PMID 22559051 DOI: 10.1021/Jo300725V  0.51
2012 Snowden TS. Recent applications of gem-dichloroepoxide intermediates in synthesis Arkivoc. 2012: 24-40. DOI: 10.3998/Ark.5550190.0013.204  0.35
2012 Ganta A, Shamshina JL, Cafiero LR, Snowden TS. Stereoselective synthesis of cis- or trans-2,4-disubstituted butyrolactones from Wynberg lactone Tetrahedron. 68: 5396-5405. DOI: 10.1016/J.Tet.2012.04.107  0.619
2009 Ganta A, Snowden TS. ChemInform Abstract: Carbocupration-Functionalization of Arynes: Rapid Access to Variably ortho-Substituted ((E)-3-Phenylprop-1-enyl)silanes. Cheminform. 40. DOI: 10.1002/chin.200915184  0.744
2008 Ganta A, Snowden TS. Carbocupration-functionalization of arynes: rapid access to variably ortho-substituted ((E)-3-phenylprop-1-enyl)silanes. Organic Letters. 10: 5103-6. PMID 18928288 DOI: 10.1021/Ol8021885  0.756
2008 Cafiero LR, Snowden TS. General and practical conversion of aldehydes to homologated carboxylic acids. Organic Letters. 10: 3853-6. PMID 18686964 DOI: 10.1021/Ol8016484  0.687
2008 Cafiero LR, Snowden TS. tert-Butyldimethylsilyloxytrichloromethylmethane-readily accessible and robust protecting group for (hetero)aryl aldehydes Tetrahedron Letters. 49: 2844-2847. DOI: 10.1016/J.Tetlet.2008.02.072  0.685
2008 Carr JM, Snowden TS. Comparative reductive desymmetrization of 2,2-disubstituted-cycloalkane-1,3-diones Tetrahedron. 64: 2897-2905. DOI: 10.1016/J.Tet.2008.01.065  0.626
2007 Ganta A, Snowden TS. Facile preparation of 2-iodophenyl trifluoromethanesulfonates: Superior aryne precursors Synlett. 2227-2231. DOI: 10.1055/S-2007-985565  0.74
2007 Shamshina JL, Snowden TS. Convergent synthesis of potent COX-2 inhibitor inotilone Tetrahedron Letters. 48: 3767-3769. DOI: 10.1016/J.Tetlet.2007.03.166  0.413
2006 Shamshina JL, Snowden TS. Practical approach to alpha- or gamma-heterosubstituted enoic acids. Organic Letters. 8: 5881-4. PMID 17134296 DOI: 10.1021/Ol0625132  0.403
2004 Zhong Z, Snowden TS, Best MD, Anslyn EV. Rate of enolate formation is not very sensitive to the hydrogen bonding ability of donors to carboxyl oxygen lone pair acceptors; a ramification of the principle of non-perfect synchronization for general-base-catalyzed enolate formation. Journal of the American Chemical Society. 126: 3488-95. PMID 15025476 DOI: 10.1021/Ja0306011  0.636
2001 Snowden TS, Bisson AP, Anslyn EV. Artificial receptors involved in enolization and pK(a) shifts. Bioorganic & Medicinal Chemistry. 9: 2467-78. PMID 11553488 DOI: 10.1016/S0968-0896(01)00222-X  0.406
1999 Snowden TS, Anslyn EV. Anion recognition: synthetic receptors for anions and their application in sensors. Current Opinion in Chemical Biology. 3: 740-6. PMID 10651521 DOI: 10.1016/S1367-5931(99)00034-4  0.373
1999 Snowden TS, Bisson AP, Anslyn EV. A comparison of NH-π versus lone pair hydrogen bonding effects on carbon acid pK(a) shifts [10] Journal of the American Chemical Society. 121: 6324-6325. DOI: 10.1021/Ja991039A  0.407
Low-probability matches (unlikely to be authored by this person)
2015 Li Z, Gupta MK, Snowden TS. One-Carbon Homologation of Primary Alcohols and the Reductive Homologation of Aldehydes Involving a Jocic-Type Reaction European Journal of Organic Chemistry. 2015: 7009-7019. DOI: 10.1002/Ejoc.201501089  0.298
2018 Mathew B, Snowden TS, Connelly MC, Guy RK, Reynolds RC. A small diversity library of α-methyl amide analogs of sulindac for probing anticancer structure-activity relationships. Bioorganic & Medicinal Chemistry Letters. PMID 29776741 DOI: 10.1016/J.Bmcl.2018.05.023  0.277
2008 Garrett S, Franco V, Snowden T, Redden C, Warke V, Bakker MG. Development of strategies to improvement ordering and perpendicular alignment of cylinder phase block copolymers used as templates for bit patterned media Materials Research Society Symposium Proceedings. 1032: 117-122. DOI: 10.1557/Proc-1032-I14-38  0.26
2007 Shamshina JL, Snowden TS. Practical Approach to α- or γ-Heterosubstituted Enoic Acids. Cheminform. 38. DOI: 10.1002/chin.200715048  0.16
2008 Snowden T, Shim KS, Schmutte C, Acharya S, Fishel R. hMSH4-hMSH5 adenosine nucleotide processing and interactions with homologous recombination machinery. The Journal of Biological Chemistry. 283: 145-54. PMID 17977839 DOI: 10.1074/Jbc.M704060200  0.086
2004 Snowden T, Acharya S, Butz C, Berardini M, Fishel R. hMSH4-hMSH5 recognizes Holliday Junctions and forms a meiosis-specific sliding clamp that embraces homologous chromosomes. Molecular Cell. 15: 437-51. PMID 15304223 DOI: 10.1016/J.Molcel.2004.06.040  0.074
2006 Snowden T. Artificial Enzymes Edited by Ronald Breslow (Columbia University). Wiley-VCH Verlag GmbH & Co. KGaA:  Weinheim. 2005. xii + 182 pp. $99.95. ISBN 3-527-31165-3. Journal of the American Chemical Society. 128: 4918-4918. DOI: 10.1021/ja0598412  0.069
2023 Khurshid R, Schulz JM, Hu J, Snowden TS, Reynolds RC, Schürer SC. Targeted degrader technologies as prospective SARS-CoV-2 therapies. Drug Discovery Today. 103847. PMID 38029836 DOI: 10.1016/j.drudis.2023.103847  0.059
2005 Lenzi ML, Smith J, Snowden T, Kim M, Fishel R, Poulos BK, Cohen PE. Extreme heterogeneity in the molecular events leading to the establishment of chiasmata during meiosis i in human oocytes. American Journal of Human Genetics. 76: 112-27. PMID 15558497 DOI: 10.1086/427268  0.035
2010 Biswas S, Snowden T, Moreno M, Nelson DA, Miller MW, Fossum TW, Criscione JC. Implantable Device To Modulate Diastolic Mechanics: Demonstration of Adjustable Support In Vivo and Recoil in Bench-Top Tests Journal of Cardiac Failure. 16: S54. DOI: 10.1016/J.Cardfail.2010.06.186  0.023
2013 Snowden T, Biswas S, Criscione J. Modulation of Diastolic Filling Using an Epicardial Diastolic Recoil Device Journal of Medical Devices. 7. DOI: 10.1115/1.4024156  0.016
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