Year |
Citation |
Score |
2010 |
Tudge M, Savarin CG, Difelice K, Maligres P, Humphrey G, Reamer B, Tellers DM, Hughes D. Development of a kilogram-scale asymmetric synthesis of a potent DP receptor antagonist Organic Process Research and Development. 14: 787-798. DOI: 10.1021/Op100008M |
0.364 |
|
2009 |
Thiel OR, Achmatowicz M, Bernard C, Wheeler P, Savarin C, Correll TL, Kasparian A, Allgeier A, Bartberger MD, Tan H, Larsen RD. Development of a practical synthesis of a p38 MAP kinase inhibitor Organic Process Research and Development. 13: 230-241. DOI: 10.1021/Op800250V |
0.324 |
|
2007 |
Savarin CG, Grisé C, Murry JA, Reamer RA, Hughes DL. Novel intramolecular reactivity of oximes: synthesis of cyclic and spiro-fused imines. Organic Letters. 9: 981-3. PMID 17319674 DOI: 10.1021/ol0630043 |
0.395 |
|
2006 |
Tudge M, Tamiya M, Savarin C, Humphrey GR. Development of a novel, highly efficient halide-catalyzed sulfenylation of indoles. Organic Letters. 8: 565-8. PMID 16468712 DOI: 10.1021/OL052615C |
0.401 |
|
2006 |
Tudge M, Tamiya M, Savarin C, Humphrey GR. Development of a Novel, Highly Efficient Halide-Catalyzed Sulfenylation of Indoles. Cheminform. 37. DOI: 10.1002/CHIN.200626111 |
0.332 |
|
2004 |
Corley EG, Conrad K, Murry JA, Savarin C, Holko J, Boice G. Direct synthesis of 4-arylpiperidines via palladium/copper(I)-cocatalyzed Negishi coupling of a 4-piperidylzinc iodide with aromatic halides and triflates. The Journal of Organic Chemistry. 69: 5120-3. PMID 15255748 DOI: 10.1021/JO049647I |
0.533 |
|
2004 |
Corley EG, Conrad K, Murry JA, Savarin C, Holko J, Boice G. Direct Synthesis of 4-Arylpiperidines via Palladium/Copper(I)-Cocatalyzed Negishi Coupling of a 4-Piperidylzinc Iodide with Aromatic Halides and Triflates. Cheminform. 35. DOI: 10.1002/CHIN.200446140 |
0.604 |
|
2002 |
Savarin C, Srogl J, Liebeskind LS. A mild, nonbasic synthesis of thioethers. The copper-catalyzed coupling of boronic acids with N-thio(alkyl, aryl, heteroaryl)imides Organic Letters. 4: 4309-4312. PMID 12443085 DOI: 10.1021/Ol026948A |
0.675 |
|
2002 |
Savarin CG, Murry JA, Dormer PG. An expedient synthesis of highly functionalized naphthyridones and quinolines from a common N-aryl pyridinone template. Organic Letters. 4: 2071-4. PMID 12049520 DOI: 10.1021/ol025950z |
0.341 |
|
2002 |
Liebeskind LS, Srogl J, Savarin C, Polanco C. Bioinspired organometallic chemistry Pure and Applied Chemistry. 74: 115-122. DOI: 10.1351/Pac200274010115 |
0.436 |
|
2001 |
Savarin C, Liebeskind LS. Nonbasic, room temperature, palladium-catalyzed coupling of aryl and alkenyl iodides with boronic acids mediated by copper(I) thiophene-2-carboxylate (CuTC). Organic Letters. 3: 2149-52. PMID 11440566 DOI: 10.1021/Ol010060P |
0.702 |
|
2001 |
Savarin C, Srogl J, Liebeskind LS. Substituted alkyne synthesis under nonbasic conditions: copper carboxylate-mediated, palladium-catalyzed thioalkyne-boronic acid cross-coupling. Organic Letters. 3: 91-3. PMID 11429881 DOI: 10.1021/Ol006807D |
0.731 |
|
2001 |
Savarin C, Liebeskind LS. Nonbasic, room temperature, palladium-catalyzed coupling of aryl and alkenyl iodides with boronic acids mediated by copper(I) thiophene-2-carboxylate (CuTC) Organic Letters. 3: 2149-2151. DOI: 10.1021/ol010060p |
0.7 |
|
2001 |
Savarin C, Srogl J, Liebeskind LS. Substituted alkyne synthesis under nonbasic conditions: Copper carboxylate-mediated, palladium-catalyzed thioalkyne-boronic acid cross-coupling Organic Letters. 3: 91-93. DOI: 10.1021/ol006807d |
0.735 |
|
2000 |
Savarin C, Srogl J, Liebeskind LS. Thiol ester-boronic acid cross-coupling. Catalysis using alkylative activation of the palladium thiolate intermediate. Organic Letters. 2: 3229-31. PMID 11009388 DOI: 10.1021/Ol000231A |
0.69 |
|
2000 |
Savarin C, Srogl J, Liebeskind LS. Thiol ester-boronic acid cross-coupling. Catalysis using alkylative activation of the palladium thiolate intermediate Organic Letters. 2: 3229-3231. |
0.695 |
|
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