Year |
Citation |
Score |
2014 |
Truong PM, Zavalij PY, Doyle MP. Highly enantioselective carbonyl-ene reactions of 2,3-diketoesters: efficient and atom-economical process to functionalized chiral α-hydroxy-β-ketoesters. Angewandte Chemie (International Ed. in English). 53: 6468-72. PMID 24846809 DOI: 10.1002/Anie.201402233 |
0.56 |
|
2014 |
Mandler MD, Truong PM, Zavalij PY, Doyle MP. Catalytic conversion of diazocarbonyl compounds to imines: applications to the synthesis of tetrahydropyrimidines and β-lactams. Organic Letters. 16: 740-3. PMID 24423056 DOI: 10.1021/Ol403427S |
0.614 |
|
2014 |
Truong PM, Mandler MD, Shanahan CS, Doyle MP. Lewis acid catalyzed diastereoselective 1,3-dipolar cycloaddition between diazoacetoacetate enones and azomethine ylides Heterocycles. 88: 1039-1049. DOI: 10.3987/Com-13-S(S)63 |
0.588 |
|
2014 |
Mandler MD, Truong PM, Zavalij PY, Doyle MP. Catalytic conversion of diazocarbonyl compounds to imines: Applications to the synthesis of tetrahydropyrimidines and β-lactams Organic Letters. 16: 740-743. DOI: 10.1021/ol403427s |
0.467 |
|
2014 |
Truong PM, Mandler MD, Doyle MP. The chemistry of vicinal tricarbonyls: An expedient route to fully-substituted 3-aminopyrroles Tetrahedron Letters. DOI: 10.1016/J.Tetlet.2014.10.139 |
0.567 |
|
2014 |
Truong PM, Zavalij PY, Doyle MP. Highly enantioselective carbonyl-ene reactions of 2,3-diketoesters: Efficient and atom-economical process to functionalized chiral α-hydroxy-β-ketoesters Angewandte Chemie - International Edition. 53: 6468-6472. DOI: 10.1002/anie.201402233 |
0.543 |
|
2013 |
Shanahan CS, Truong P, Mason SM, Leszczynski JS, Doyle MP. Diazoacetoacetate enones for the synthesis of diverse natural product-like scaffolds. Organic Letters. 15: 3642-5. PMID 23829448 DOI: 10.1021/Ol4015199 |
0.553 |
|
2013 |
Truong PM, Mandler MD, Zavalij PY, Doyle MP. Tetrahydroquinolines and benzazepines through catalytic diastereoselective formal [4 + 2]-cycloaddition reactions between donor-acceptor cyclopropenes and imines Organic Letters. 15: 3278-3281. PMID 23777207 DOI: 10.1021/Ol401308D |
0.577 |
|
2012 |
Truong P, Shanahan CS, Doyle MP. Divergent stereocontrol of acid catalyzed intramolecular aldol reactions of 2,3,7-triketoesters: Synthesis of highly functionalized cyclopentanones Organic Letters. 14: 3608-3611. PMID 22738671 DOI: 10.1021/Ol301317A |
0.58 |
|
2012 |
Truong P, Shanahan CS, Doyle MP. ChemInform Abstract: Divergent Stereocontrol of Acid Catalyzed Intramolecular Aldol Reactions of 2,3,7-Triketoesters: Synthesis of Highly Functionalized Cyclopentanones. Cheminform. 43: no-no. DOI: 10.1002/chin.201246056 |
0.539 |
|
2011 |
Truong P, Xu X, Doyle MP. An efficient methodology to substituted furans via oxidation of functionalized α-diazo-β-ketoacetates. Tetrahedron Letters. 52: 2093-2096. PMID 21516185 DOI: 10.1016/J.Tetlet.2010.11.166 |
0.563 |
|
2011 |
Truong P, Xu X, Doyle MP. ChemInform Abstract: An Efficient Methodology to Substituted Furans via Oxidation of Functionalized α-Diazo-β-ketoacetates. Cheminform. 42: no-no. DOI: 10.1002/chin.201132088 |
0.37 |
|
2011 |
Baumstark AL, Kennedy GD, Vasquez PC, Desalegn N, Truong P. ChemInform Abstract: Synthesis of Hexa(methyl/phenyl) Substituted Pyrazolines and Thermolysis to Hexasubstituted Cyclopropanes. Cheminform. 42: no-no. DOI: 10.1002/chin.201105114 |
0.303 |
|
2010 |
Baumstark AL, Kennedy GD, Vasquez PC, Desalegn N, Truong P. Synthesis of hexa(methyl/phenyl) substituted pyrazolines and thermolysis to hexasubstituted cyclopropanes Journal of Heterocyclic Chemistry. 47: 1255-1258. DOI: 10.1002/Jhet.266 |
0.346 |
|
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