| Year |
Citation |
Score |
| 2019 |
Jung H, Choi Y, Lee D, Seo JK, Kee JM. Distinct phosphorylation and dephosphorylation dynamics of protein arginine kinases revealed by fluorescent activity probes. Chemical Communications (Cambridge, England). PMID 31184653 DOI: 10.1039/C9Cc03285A |
0.424 |
|
| 2019 |
Maiti S, Kim J, Park JH, Nam D, Lee JB, Kim YJ, Kee JM, Seo JK, Myung K, Rohde JU, Choe W, Kwon OH, Hong SY. Chemoselective Trifluoroethylation Reactions of Quinazolinones and Identification of Photostability. The Journal of Organic Chemistry. PMID 31050290 DOI: 10.1021/Acs.Joc.9B00470 |
0.334 |
|
| 2019 |
Choi Y, Shin SH, Jung H, Kwon O, Seo JK, Kee JM. A specific fluorescent probe for protein histidine phosphatase activity. Acs Sensors. PMID 30912641 DOI: 10.1021/Acssensors.9B00242 |
0.383 |
|
| 2018 |
Jung H, Shin SH, Kee JM. Recent Updates on Protein N-phosphoramidate hydrolases. Chembiochem : a European Journal of Chemical Biology. PMID 30371011 DOI: 10.1002/Cbic.201800566 |
0.408 |
|
| 2017 |
Kim WG, Kang ME, Lee JB, Jeon MH, Lee S, Lee J, Choi B, Cal PMSD, Kang S, Kee JM, Bernardes GJL, Rohde JU, Choe W, Hong SY. Nickel-Catalyzed Azide-Alkyne Cycloaddition to Access 1,5-Disubstituted 1,2,3-Triazoles in Air and Water. Journal of the American Chemical Society. PMID 28814075 DOI: 10.1021/Jacs.7B06338 |
0.329 |
|
| 2017 |
Oslund RC, Su X, Haugbro M, Kee JM, Esposito M, David Y, Wang B, Ge E, Perlman DH, Kang Y, Muir TW, Rabinowitz JD. Bisphosphoglycerate mutase controls serine pathway flux via 3-phosphoglycerate. Nature Chemical Biology. PMID 28805803 DOI: 10.1038/Nchembio.2453 |
0.604 |
|
| 2015 |
Kee JM, Oslund RC, Couvillon AD, Muir TW. A second-generation phosphohistidine analog for production of phosphohistidine antibodies. Organic Letters. 17: 187-9. PMID 25531910 DOI: 10.1021/Ol503320P |
0.568 |
|
| 2014 |
Wender PA, Axtman AD, Golden JE, Kee JM, Sirois LE, Quiroz RV, Stevens MC. Function through bio-inspired, synthesis-informed design: step-economical syntheses of designed kinase inhibitors†Dedicated to Max Malacria, a friend and scholar whose science and creative contributions to step-economical synthesis have inspired us all and moved the field closer to the ideal.‡Electronic supplementary information (ESI) available: Synthetic procedures and spectral data. See DOI: 10.1039/c4qo00228hClick here for additional data file. Organic Chemistry Frontiers : An International Journal of Organic Chemistry / Royal Society of Chemistry. 1: 1166-1171. PMID 25632347 DOI: 10.1039/C4Qo00228H |
0.662 |
|
| 2014 |
Oslund RC, Kee JM, Couvillon AD, Bhatia VN, Perlman DH, Muir TW. A phosphohistidine proteomics strategy based on elucidation of a unique gas-phase phosphopeptide fragmentation mechanism. Journal of the American Chemical Society. 136: 12899-911. PMID 25156620 DOI: 10.1021/Ja507614F |
0.544 |
|
| 2013 |
Kee JM, Oslund RC, Perlman DH, Muir TW. A pan-specific antibody for direct detection of protein histidine phosphorylation. Nature Chemical Biology. 9: 416-21. PMID 23708076 DOI: 10.1038/Nchembio.1259 |
0.588 |
|
| 2012 |
Kee JM, Muir TW. Chasing phosphohistidine, an elusive sibling in the phosphoamino acid family. Acs Chemical Biology. 7: 44-51. PMID 22148577 DOI: 10.1021/Cb200445W |
0.539 |
|
| 2011 |
Wender PA, Buschmann N, Cardin NB, Jones LR, Kan C, Kee JM, Kowalski JA, Longcore KE. Gateway synthesis of daphnane congeners and their protein kinase C affinities and cell-growth activities. Nature Chemistry. 3: 615-9. PMID 21778981 DOI: 10.1038/Nchem.1074 |
0.688 |
|
| 2010 |
Kee JM, Villani B, Carpenter LR, Muir TW. Development of stable phosphohistidine analogues. Journal of the American Chemical Society. 132: 14327-9. PMID 20879710 DOI: 10.1021/Ja104393T |
0.597 |
|
| 2008 |
Wender PA, Kee JM, Warrington JM. Practical synthesis of prostratin, DPP, and their analogs, adjuvant leads against latent HIV. Science (New York, N.Y.). 320: 649-52. PMID 18451298 DOI: 10.1126/Science.1154690 |
0.502 |
|
| 2006 |
Wender PA, Bi FC, Buschmann N, Gosselin F, Kan C, Kee JM, Ohmura H. Studies on oxidopyrylium [5+2] cycloadditions: toward a general synthetic route to the C12-hydroxydaphnetoxins. Organic Letters. 8: 5373-6. PMID 17078721 DOI: 10.1021/Ol062234E |
0.662 |
|
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