Year |
Citation |
Score |
2016 |
Javed MS, Han X, Hu C, Zhou M, Huang Z, Tang X, Gu X. Tracking pseudocapacitive contribution to superior energy storage of MnS nanoparticles grown on carbon textile. Acs Applied Materials & Interfaces. PMID 27559608 DOI: 10.1021/Acsami.6B07924 |
0.512 |
|
2016 |
Golani LK, Wallace-Povirk A, Deis SM, Wong JE, Ke J, Gu X, Raghavan S, Wilson MR, Li X, Polin LA, de Waal PW, White K, Kushner J, O'Connor CE, Hou Z, et al. Tumor Targeting with Novel 6-Substituted Pyrrolo [2,3-d] Pyrimidine Antifolates with Heteroatom Bridge Substitutions Via Cellular Uptake by Folate Receptor α and the Proton-coupled Folate Transporter and Inhibition of De Novo Purine Nucleotide Biosynthesis. Journal of Medicinal Chemistry. PMID 27458733 DOI: 10.1021/Acs.Jmedchem.6B00594 |
0.3 |
|
2012 |
Liu Z, Mehta SJ, Lee KS, Grossman B, Qu H, Gu X, Nichol GS, Hruby VJ. Thio-Claisen rearrangement used in preparing anti-β-functionalized γ,δ-unsaturated amino acids: scope and limitations. The Journal of Organic Chemistry. 77: 1289-300. PMID 22283513 DOI: 10.1021/Jo201753Q |
0.754 |
|
2010 |
Liu Z, Qu H, Gu X, Lee KS, Grossman B, Kumirov VK, Hruby VJ. Novel anti-β-functionalized γ,δ-unsaturated amino acids via a thio-Claisen rearrangement Tetrahedron Letters. 51: 3518-3520. DOI: 10.1016/J.Tetlet.2010.04.102 |
0.727 |
|
2010 |
Liu Z, Qu H, Gu X, Lee K, Grossman B, Kumirov VK, Hruby VJ. ChemInform Abstract: Novel anti-β-Functionalized γ,δ-Unsaturated Amino Acids via a Thio-Claisen Rearrangement. Cheminform. 41: no-no. DOI: 10.1002/chin.201043191 |
0.557 |
|
2009 |
Liu Z, Qu H, Gu X, Min BJ, Nyberg J, Hruby VJ. Enantioselective synthesis of anti-β-substituted γ,δ- unsaturated amino acids: A highly selective asymmetric Thio-Claisen rearrangement (Organic Letters (2008) 10) Organic Letters. 11: 497. DOI: 10.1021/Ol8027913 |
0.778 |
|
2009 |
Liu Z, Qu H, Gu X, Min BJ, Nyberg J, Hruby VJ. ChemInform Abstract: Enantioselective Synthesis of anti-β-Substituted γ,δ-Unsaturated Amino Acids: A Highly Selective Asymmetric Thio-Claisen Rearrangement. Cheminform. 40. DOI: 10.1002/chin.200904186 |
0.63 |
|
2008 |
Min BJ, Gu X, Yamamoto T, Petrov RR, Qu H, Lee YS, Hruby VJ. Synthesis of a novel benzyl-octahydropyrazino[1,2-a]pyrimidin-6-one derivative as a convenient internal bicyclic peptidomimetic. Tetrahedron Letters. 49: 2316-2319. PMID 19340283 DOI: 10.1016/J.Tetlet.2008.01.137 |
0.771 |
|
2008 |
Liu Z, Qu H, Gu X, Min BJ, Nichol GS, Nyberg J, Hruby VJ. Enantioselective synthesis of anti-beta-substituted gamma,delta-unsaturated amino acids: a highly selective asymmetric thio-Claisen rearrangement. Organic Letters. 10: 4105-8. PMID 18702500 DOI: 10.1021/Ol801657Q |
0.776 |
|
2008 |
Sutton GM, Josephine Babin M, Gu X, Hruby VJ, Butler AA. A derivative of the melanocortin receptor antagonist SHU9119 (PG932) increases food intake when administered peripherally. Peptides. 29: 104-11. PMID 18054119 DOI: 10.1016/J.Peptides.2007.10.014 |
0.418 |
|
2008 |
Qu H, Gu X, Liu Z, Min BJ, Hruby VJ. ChemInform Abstract: Asymmetric Eschenmoser-Claisen Rearrangement for anti-β-Substituted γ,δ-Unsaturated Amino Acids. Cheminform. 39. DOI: 10.1002/chin.200812203 |
0.587 |
|
2007 |
Qu H, Gu X, Liu Z, Min BJ, Hruby VJ. Asymmetric Eschenmoser-Claisen rearrangement for anti-beta-substituted gamma,delta-unsaturated amino acids. Organic Letters. 9: 3997-4000. PMID 17760455 DOI: 10.1021/Ol701704H |
0.743 |
|
2006 |
Carducci MD, Gu X, Cole JR, Hruby VJ. [N-({(R)-2-[(N-Benzylprolyl)amino]phenyl}-phenylmethylene)-2(S)-(pent-4-enyl)-glycinato]nickel(II). Acta Crystallographica. Section E, Structure Reports Online. 62: m1219-m1220. PMID 17268578 DOI: 10.1107/S160053680601244X |
0.45 |
|
2006 |
Ying J, Gu X, Cai M, Dedek M, Vagner J, Trivedi DB, Hruby VJ. Design, synthesis, and biological evaluation of new cyclic melanotropin peptide analogues selective for the human melanocortin-4 receptor. Journal of Medicinal Chemistry. 49: 6888-96. PMID 17154518 DOI: 10.1021/Jm060768F |
0.714 |
|
2006 |
Qu H, Gu X, Min BJ, Liu Z, Hruby VJ. Synthesis of Anti-beta-substituted gamma,delta-unsaturated amino acids via Eschenmoser-Claisen rearrangement. Organic Letters. 8: 4215-8. PMID 16956190 DOI: 10.1021/Ol061414L |
0.746 |
|
2005 |
Gu X, Ying J, Min B, Cain JP, Davis P, Willey P, Navratilova E, Yamamura HI, Porreca F, Hruby VJ. Parallel synthesis and biological evaluation of different sizes of bicyclo[2,3]-Leu-enkephalin analogues. Biopolymers. 80: 151-63. PMID 15660379 DOI: 10.1002/Bip.20208 |
0.754 |
|
2004 |
Gu X, Ying J, Agnes RS, Navratilova E, Davis P, Stahl G, Porreca F, Yamamura HI, Hruby VJ. Novel design of bicyclic beta-turn dipeptides on solid-phase supports and synthesis of [3.3.0]-Bicyclo([2,3])-leu-enkephalin analogues. Organic Letters. 6: 3285-8. PMID 15355033 DOI: 10.1021/Ol0488183 |
0.765 |
|
2004 |
Ndungu JM, Gu X, Gross DE, Cain JP, Carducci MD, Hruby VJ. Synthesis of bicyclic dipeptide mimetics for the cholecystokinin and opioid receptors Tetrahedron Letters. 45: 4139-4142. DOI: 10.1016/J.Tetlet.2004.03.146 |
0.796 |
|
2004 |
Ndungu JM, Gu X, Gross DE, Ying J, Hruby VJ. A simple and efficient synthesis of an Asp-Gly dipeptide mimetic Tetrahedron Letters. 45: 3245-3247. DOI: 10.1016/J.Tetlet.2004.02.117 |
0.797 |
|
2004 |
Gu X, Ndungu JM, Qiu W, Ying J, Carducci MD, Wooden H, Hruby VJ. Large scale enantiomeric synthesis, purification, and characterization of ω-unsaturated amino acids via a Gly-Ni(II)-BPB-complex Tetrahedron. 60: 8233-8243. DOI: 10.1016/J.Tet.2004.06.087 |
0.788 |
|
2003 |
Ying J, Kövér KE, Gu X, Han G, Trivedi DB, Kavarana MJ, Hruby VJ. Solution structures of cyclic melanocortin agonists and antagonists by NMR. Biopolymers. 71: 696-716. PMID 14991679 DOI: 10.1002/Bip.10596 |
0.691 |
|
2003 |
Cowell SM, Gu X, Vagner J, Hruby VJ. Intelligent design in combinatorial chemistry: use of designed peptide libraries to explore secondary and tertiary structures in peptides and proteins. Methods in Enzymology. 369: 288-97. PMID 14722960 DOI: 10.1016/S0076-6879(03)69016-6 |
0.485 |
|
2003 |
Gu X, Cowell S, Ying J, Tang X, Hruby VJ. Synthesis of β-phenyl-δ,ε-unsaturated amino acids and stereoselective introduction of side chain groups into [4,3,0]-bicyclic β-turn dipeptides Tetrahedron Letters. 44: 5863-5866. DOI: 10.1016/S0040-4039(03)01383-2 |
0.725 |
|
2002 |
Gu X, Tang X, Cowell S, Ying J, Hruby VJ. A novel strategy toward [6,5]-bicyclic β-turn dipeptide Tetrahedron Letters. 43: 6669-6672. DOI: 10.1016/S0040-4039(02)01338-2 |
0.724 |
|
2001 |
Qiu W, Gu X, Soloshonok VA, Carducci MD, Hruby VJ. Stereoselective synthesis of conformationally constrained reverse turn dipeptide mimetics Tetrahedron Letters. 42: 145-148. DOI: 10.1016/S0040-4039(00)01864-5 |
0.577 |
|
2001 |
Qiu W, Gu X, Soloshonok VA, Carducci MD, Hruby VJ. ChemInform Abstract: Stereoselective Synthesis of Conformationally Constrained Reverse Turn Dipeptide Mimetics Cheminform. 32: no-no. DOI: 10.1002/chin.200116194 |
0.499 |
|
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