Year |
Citation |
Score |
2017 |
Singh MK, Waybright J, Zhang Q. A facile method to enable a model phospholipid cell-permeable and photoactivatable Tetrahedron. 73: 3677-3683. DOI: 10.1016/J.Tet.2017.04.026 |
0.31 |
|
2015 |
Huang W, Zhang Q. Fluorous photoaffinity labeling to probe protein-small molecule interactions. Methods in Molecular Biology (Clifton, N.J.). 1263: 253-61. PMID 25618351 DOI: 10.1007/978-1-4939-2269-7_20 |
0.311 |
|
2014 |
Huang W, Proctor A, Sims CE, Allbritton NL, Zhang Q. Fluorous enzymatic synthesis of phosphatidylinositides. Chemical Communications (Cambridge, England). 50: 2928-31. PMID 24496473 DOI: 10.1039/C4Cc00022F |
0.361 |
|
2013 |
Huang W, Barrett M, Hajicek N, Hicks S, Harden TK, Sondek J, Zhang Q. Small molecule inhibitors of phospholipase C from a novel high-throughput screen. The Journal of Biological Chemistry. 288: 5840-8. PMID 23297405 DOI: 10.1074/Jbc.M112.422501 |
0.338 |
|
2012 |
Wang X, Barrett M, Sondek J, Harden TK, Zhang Q. Fluorescent phosphatidylinositol 4,5-bisphosphate derivatives with modified 6-hydroxy group as novel substrates for phospholipase C. Biochemistry. 51: 5300-6. PMID 22703043 DOI: 10.1021/Bi300637H |
0.328 |
|
2011 |
Song Z, Zhang Q. Design, synthesis, and incorporation of fluorous 5-methylcytosines into oligonucleotides. The Journal of Organic Chemistry. 76: 10263-8. PMID 22082055 DOI: 10.1021/Jo2015399 |
0.347 |
|
2011 |
Huang W, Jiang D, Wang X, Wang K, Sims CE, Allbritton NL, Zhang Q. Kinetic analysis of PI3K reactions with fluorescent PIP2 derivatives. Analytical and Bioanalytical Chemistry. 401: 1881-8. PMID 21789487 DOI: 10.1007/S00216-011-5257-Z |
0.325 |
|
2011 |
Huang W, Hicks SN, Sondek J, Zhang Q. A fluorogenic, small molecule reporter for mammalian phospholipase C isozymes. Acs Chemical Biology. 6: 223-8. PMID 21158426 DOI: 10.1021/Cb100308N |
0.327 |
|
2006 |
Curran DP, Zhang Q, Lu H, Gudipati V. On the proof and disproof of natural product stereostructures: characterization and analysis of a twenty-eight member stereoisomer library of murisolins and their Mosher ester derivatives. Journal of the American Chemical Society. 128: 9943-56. PMID 16866554 DOI: 10.1021/Ja062469L |
0.649 |
|
2006 |
Curran DP, Zhang Q, Richard C, Lu H, Gudipati V, Wilcox CS. Total synthesis of a 28-member stereoisomer library of murisolins. Journal of the American Chemical Society. 128: 9561-73. PMID 16848495 DOI: 10.1021/Ja061801Q |
0.678 |
|
2005 |
Zhang Q, Curran DP. Quasienantiomers and quasiracemates: new tools for identification, analysis, separation, and synthesis of enantiomers. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 4866-80. PMID 15915521 DOI: 10.1002/Chem.200500076 |
0.523 |
|
2005 |
Curran DP, Wang X, Zhang Q. Light, medium, and heavy fluorous triarylphosphines exhibit comparable reactivities to triphenylphosphine in typical reactions of triarylphosphines. The Journal of Organic Chemistry. 70: 3716-9. PMID 15845013 DOI: 10.1021/Jo050116J |
0.507 |
|
2004 |
Zhang Q, Lu H, Richard C, Curran DP. Fluorous mixture synthesis of stereoisomer libraries: total syntheses of (+)-murisolin and fifteen diastereoisomers. Journal of the American Chemical Society. 126: 36-7. PMID 14709047 DOI: 10.1021/Ja038542E |
0.539 |
|
2003 |
Vallin KS, Zhang Q, Larhed M, Curran DP, Hallberg A. A new regioselective Heck vinylation with enamides. Synthesis and investigation of fluorous-tagged bidentate ligands for fast separation. The Journal of Organic Chemistry. 68: 6639-45. PMID 12919028 DOI: 10.1021/Jo034265I |
0.484 |
|
2003 |
Curran DP, Zhang Q. Microwave Heating Effects Rapid and Selective Decarboalkoxylation of Mono-Alkylated Malonates and β-Ketoesters Advanced Synthesis and Catalysis. 345: 329-332. DOI: 10.1002/Adsc.200390033 |
0.45 |
|
2002 |
Zhang Q, Rivkin A, Curran DP. Quasiracemic synthesis: concepts and implementation with a fluorous tagging strategy to make both enantiomers of pyridovericin and mappicine. Journal of the American Chemical Society. 124: 5774-81. PMID 12010052 DOI: 10.1021/Ja025606X |
0.654 |
|
2001 |
Luo Z, Zhang Q, Oderaotoshi Y, Curran DP. Fluorous mixture synthesis: a fluorous-tagging strategy for the synthesis and separation of mixtures of organic compounds. Science (New York, N.Y.). 291: 1766-9. PMID 11230688 DOI: 10.1126/Science.1057567 |
0.625 |
|
2000 |
Zhang Q, Luo Z, Curran DP. Separation of "light fluorous" reagents and catalysts by fluorous solid-phase extraction: synthesis and study of a family of triarylphosphines bearing linear and branched fluorous tags. The Journal of Organic Chemistry. 65: 8866-73. PMID 11149827 DOI: 10.1021/Jo000464F |
0.599 |
|
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