Year |
Citation |
Score |
2015 |
Du K, Luo Z, Guo P, Tang W, Wu N, Zheng P, Du W, Zeng A, Jing W, Chang C, Fu Q. Preparation and evaluation of a molecularly imprinted sol-gel material as the solid-phase extraction adsorbents for the specific recognition of cloxacilloic acid in cloxacillin. Journal of Separation Science. PMID 26592970 DOI: 10.1002/jssc.201500961 |
0.476 |
|
2015 |
Tian D, Luo Z, Zhou M, Li M, Yu L, Wang C, Yuan J, Li F, Tian B, Sui B, Chen H, Fu ZF, Zhao L. The critical role of K1685 and K1829 in the large protein of rabies virus on viral pathogenicity and immune evasion. Journal of Virology. PMID 26468538 DOI: 10.1128/JVI.02050-15 |
0.477 |
|
2015 |
Luo Z, Tian D, Zhou M, Xiao W, Zhang Y, Li M, Sui B, Wang W, Guan H, Chen H, Fu ZF, Zhao L. λ-Carrageenan P32 Is a Potent Inhibitor of Rabies Virus Infection. Plos One. 10: e0140586. PMID 26465753 DOI: 10.1371/journal.pone.0140586 |
0.483 |
|
2010 |
Curran DP, Hadida S, Kim S, Luo Z. ChemInform Abstract: Fluorous Tin Hydrides: A New Family of Reagents for Use and Reuse in Radical Reactions. Cheminform. 30: no-no. DOI: 10.1002/chin.199947187 |
0.406 |
|
2010 |
Ryu I, Niguma T, Minakata S, Komatsu M, Luo Z, Curran DP. ChemInform Abstract: Radical Carbonylations with Fluorous Allyltin Reagents. Cheminform. 30: no-no. DOI: 10.1002/chin.199925071 |
0.392 |
|
2010 |
KAINZ S, LUO Z, CURRAN DP, LEITNER W. ChemInform Abstract: Synthesis of Perfluoroalkyl-Substituted Aryl Bromides and Their Purification over Fluorous Reverse Phase Silica. Cheminform. 30: no-no. DOI: 10.1002/chin.199904080 |
0.468 |
|
2003 |
Curran DP, Amatore M, Guthrie D, Campbell M, Go E, Luo Z. Synthesis and reactions of fluorous carbobenzyloxy (FCbz) derivatives of alpha-amino acids. The Journal of Organic Chemistry. 68: 4643-7. PMID 12790566 DOI: 10.1021/Jo0344283 |
0.654 |
|
2002 |
Zhang W, Luo Z, Chen CH, Curran DP. Solution-phase preparation of a 560-compound library of individual pure mappicine analogues by fluorous mixture synthesis. Journal of the American Chemical Society. 124: 10443-50. PMID 12197746 DOI: 10.1021/Ja026947D |
0.548 |
|
2002 |
Luo Z, Swaleh SM, Theil F, Curran DP. Resolution of 1-(2-naphthyl)ethanol by a combination of an enzyme-catalyzed kinetic resolution with a fluorous triphasic separative reaction. Organic Letters. 4: 2585-7. PMID 12123382 DOI: 10.1021/Ol026232F |
0.476 |
|
2001 |
Luo Z, Williams J, Read RW, Curran DP. Fluorous Boc ((F)Boc) carbamates: new amine protecting groups for use in fluorous synthesis. The Journal of Organic Chemistry. 66: 4261-6. PMID 11397162 DOI: 10.1021/Jo010111W |
0.509 |
|
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 |
0.644 |
|
2001 |
Ryu I, Kreimerman S, Niguma T, Minakata S, Komatsu M, Luo Z, Curran DP. Synthesis of perfluorinated allylic compounds by radical allylation and their purification over fluorous reverse-phase silica Tetrahedron Letters. 42: 947-950. DOI: 10.1016/S0040-4039(00)02153-5 |
0.535 |
|
2001 |
Ryu I, Kreimerman S, Niguma T, Minakata S, Komatsu M, Luo Z, Curran DP. ChemInform Abstract: Synthesis of Perfluorinated Allylic Compounds by Radical Allylation and Their Purification over Fluorous Reverse-Phase Silica. Cheminform. 32: no-no. DOI: 10.1002/chin.200120067 |
0.489 |
|
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 |
0.65 |
|
1999 |
Curran DP, Luo Z. Fluorous Synthesis with Fewer Fluorines (Light Fluorous Synthesis): Separation of Tagged from Untagged Products by Solid-Phase Extraction with Fluorous Reverse-Phase Silica Gel Journal of the American Chemical Society. 121: 9069-9072. DOI: 10.1021/Ja991496R |
0.54 |
|
1999 |
Curran DP, Hadida S, Kim S, Luo Z. Fluorous Tin Hydrides: A New Family of Reagents for Use and Reuse in Radical Reactions Journal of the American Chemical Society. 121: 6607-6615. DOI: 10.1021/Ja990069A |
0.57 |
|
1999 |
Ryu I, Niguma T, Minakata S, Komatsu M, Luo Z, Curran DP. Radical carbonylations with fluorous allyltin reagents Tetrahedron Letters. 40: 2367-2370. DOI: 10.1016/S0040-4039(99)00188-4 |
0.487 |
|
1998 |
Curran DP, Luo Z, Degenkolb P. "Propylene spaced" allyl tin reagents: a new class of fluorous tin reagents for allylations under radical and metal-catalyzed conditions. Bioorganic & Medicinal Chemistry Letters. 8: 2403-8. PMID 9873550 DOI: 10.1016/S0960-894X(98)00435-1 |
0.492 |
|
1998 |
Kainz S, Luo Z, Curran DP, Leitner W. Synthesis of Perfluoroalkyl-Substituted Aryl Bromides and Their Purification Over Fluorous Reverse Phase Silica Synthesis. 1998: 1425-1427. DOI: 10.1055/S-1998-2186 |
0.5 |
|
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