Year |
Citation |
Score |
2010 |
Wang W, Xiong C, Zhang J, Hruby VJ. ChemInform Abstract: Practical, Asymmetric Synthesis of Aromatic-Substituted Bulky and Hydrophobic Tryptophan and Phenylalanine Derivatives. Cheminform. 33: no-no. DOI: 10.1002/chin.200235176 |
0.654 |
|
2010 |
Wang W, Zhang J, Xiong C, Hruby VJ. ChemInform Abstract: Design and Synthesis of Hydrophobic, Bulky χ2-Constrained Phenylalanine and Naphthylalanine Derivatives. Cheminform. 33: no-no. DOI: 10.1002/chin.200227225 |
0.635 |
|
2007 |
Davis FA, Xu H, Zhang J. Asymmetric synthesis of ring functionalized trans-2,6-disubstituted piperidines from N-sulfinyl delta-amino beta-keto phosphonates. total synthesis of (-)-myrtine. The Journal of Organic Chemistry. 72: 2046-52. PMID 17305397 DOI: 10.1021/Jo062365T |
0.387 |
|
2006 |
Davis FA, Xu H, Wu Y, Zhang J. Asymmetric synthesis of polyfunctionalized pyrrolidines from sulfinimine-derived pyrrolidine 2-phosphonates. Synthesis of pyrrolidine 225C. Organic Letters. 8: 2273-6. PMID 16706504 DOI: 10.1021/Ol060521C |
0.338 |
|
2005 |
Davis FA, Zhang J, Li Y, Xu H, DeBrosse C. Asymmetric synthesis of 2,4,5-trisubstituted piperidines from sulfinimine-derived δ-amino β-ketoesters. Formal synthesis of pseudodistomin B triacetate Journal of Organic Chemistry. 70: 5413-5419. PMID 15989321 DOI: 10.1021/Jo050373O |
0.411 |
|
2004 |
Davis FA, Wu Y, Xu H, Zhang J. Asymmetric synthesis of cis-5-substituted pyrrolidine 2-phosphonates using metal carbenoid NH insertion and δ-amino β-ketophosphonates Organic Letters. 6: 4523-4525. PMID 15548066 DOI: 10.1021/Ol048157+ |
0.357 |
|
2003 |
Zhang J, Xiong C, Ying J, Wang W, Hruby VJ. Stereoselective synthesis of novel dipeptide beta-turn mimetics targeting melanocortin peptide receptors. Organic Letters. 5: 3115-8. PMID 12916995 DOI: 10.1021/Ol0351347 |
0.724 |
|
2003 |
Xiong C, Zhang J, Davis P, Wang W, Ying J, Porreca F, Hruby VJ. Stereoselective synthesis of individual isomers of Leu-enkephalin analogues containing substituted beta-turn bicyclic dipeptide mimetics. Chemical Communications (Cambridge, England). 1598-9. PMID 12868772 DOI: 10.1039/B302235H |
0.738 |
|
2003 |
Zhang J, Wang W, Xiong C, Hruby VJ. Efficient and Stereoselective Synthesis of Novel cis-4-Substituted Proline Analogues. Cheminform. 34. DOI: 10.1016/S0040-4039(02)02865-4 |
0.672 |
|
2003 |
Zhang J, Wang W, Xiong C, Hruby VJ. Efficient and stereoselective synthesis of novel cis-4-substituted proline analogues Tetrahedron Letters. 44: 1413-1415. DOI: 10.1016/S0040-4039(02)02865-4 |
0.631 |
|
2003 |
Wang W, Cai M, Xiong C, Zhang J, Trivedi D, Hruby VJ. Design and Synthesis of Novel χ2-Constrained Phenylalanine, Naphthylalanine, and Tryptophan Analogues and Their Use in Biologically Active Melanotropin Peptides. Cheminform. 34. DOI: 10.1016/S0040-4020(02)00588-4 |
0.753 |
|
2002 |
Zhang J, Xiong C, Wang W, Ying J, Hruby VJ. Stereoselective bromination-suzuki cross-coupling of dehydroamino acids to form novel reverse-turn peptidomimetics: substituted unsaturated and saturated indolizidinone amino acids. Organic Letters. 4: 4029-32. PMID 12423078 DOI: 10.1021/Ol020160A |
0.717 |
|
2002 |
Wang W, Yang J, Ying J, Xiong C, Zhang J, Cai C, Hruby VJ. Stereoselective synthesis of dipeptide beta-turn mimetics: 7-benzyl and 8-phenyl substituted azabicyclo[4.3.0]nonane amino acid esters. The Journal of Organic Chemistry. 67: 6353-60. PMID 12201753 DOI: 10.1021/Jo0203591 |
0.747 |
|
2002 |
Wang W, Zhang J, Xiong C, Hruby VJ. Design and synthesis of hydrophobic, bulky χ2-constrained phenylalanine and naphthylalanine derivatives Tetrahedron Letters. 43: 2137-2140. DOI: 10.1016/S0040-4039(02)00249-6 |
0.719 |
|
2002 |
Wang W, Cai M, Xiong C, Zhang J, Trivedi D, Hruby VJ. Design and synthesis of novel χ2-constrained phenylalanine, naphthylalanine, and tryptophan analogues and their use in biologically active melanotropin peptides Tetrahedron. 58: 7365-7374. DOI: 10.1016/S0040-4020(02)00588-4 |
0.68 |
|
2002 |
Wang W, Xiong C, Zhang J, Hruby VJ. Practical, asymmetric synthesis of aromatic-substituted bulky and hydrophobic tryptophan and phenylalanine derivatives Tetrahedron. 58: 3101-3110. DOI: 10.1016/S0040-4020(02)00162-X |
0.729 |
|
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