| Year |
Citation |
Score |
| 2013 |
Huang X, Cheng CC, Fischmann TO, Duca JS, Richards M, Tadikonda PK, Reddy PA, Zhao L, Siddiqui MA, Parry D, Davis N, Seghezzi W, Wiswell D, Shipps GW. Structure-based design and optimization of 2-aminothiazole-4-carboxamide as a new class of CHK1 inhibitors. Bioorganic & Medicinal Chemistry Letters. 23: 2590-4. PMID 23535330 DOI: 10.1016/j.bmcl.2013.02.108 |
0.48 |
|
| 2008 |
Altman RA, Hyde AM, Huang X, Buchwald SL. Orthogonal Pd- and Cu-based catalyst systems for C- and N-arylation of oxindoles. Journal of the American Chemical Society. 130: 9613-20. PMID 18588302 DOI: 10.1021/Ja803179S |
0.726 |
|
| 2007 |
Zheng N, Anderson KW, Huang X, Nguyen HN, Buchwald SL. A palladium-catalyzed regiospecific synthesis of N-aryl benzimidazoles. Angewandte Chemie (International Ed. in English). 46: 7509-12. PMID 17722125 DOI: 10.1002/Anie.200702542 |
0.708 |
|
| 2007 |
Huang X, Ying JY. Asymmetric transfer hydrogenation over Ru-TsDPEN catalysts supported on siliceous mesocellular foam Chemical Communications. 1825-1827. PMID 17476400 DOI: 10.1039/B615564B |
0.371 |
|
| 2006 |
Burgos CH, Barder TE, Huang X, Buchwald SL. Significantly improved method for the pd-catalyzed coupling of phenols with aryl halides: understanding ligand effects. Angewandte Chemie (International Ed. in English). 45: 4321-6. PMID 16733839 DOI: 10.1002/Anie.200601253 |
0.737 |
|
| 2005 |
Vorogushin AV, Huang X, Buchwald SL. Use of tunable ligands allows for intermolecular Pd-catalyzed C--O bond formation. Journal of the American Chemical Society. 127: 8146-9. PMID 15926842 DOI: 10.1021/Ja050471R |
0.59 |
|
| 2003 |
Nguyen HN, Huang X, Buchwald SL. The first general palladium catalyst for the Suzuki-Miyaura and carbonyl enolate coupling of aryl arenesulfonates. Journal of the American Chemical Society. 125: 11818-9. PMID 14505394 DOI: 10.1021/Ja036947T |
0.638 |
|
| 2003 |
Huang X, Anderson KW, Zim D, Jiang L, Klapars A, Buchwald SL. Expanding Pd-catalyzed C-N bond-forming processes: the first amidation of aryl sulfonates, aqueous amination, and complementarity with Cu-catalyzed reactions. Journal of the American Chemical Society. 125: 6653-5. PMID 12769573 DOI: 10.1021/Ja035483W |
0.735 |
|
| 2003 |
Huang X, Anderson KW, Zim D, Jiang L, Klapars aA, Buchwald SL. Expanding Pd-Catalyzed C−N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed Reactions [J. Am. Chem. Soc. 2003, 125, 6653−6655]. Journal of the American Chemical Society. 125: 10767-10767. DOI: 10.1021/Ja033450A |
0.695 |
|
| 2002 |
Harris MC, Huang X, Buchwald SL. Improved functional group compatibility in the palladium-catalyzed synthesis of aryl amines. Organic Letters. 4: 2885-8. PMID 12182580 DOI: 10.1021/Ol0262688 |
0.688 |
|
| 2002 |
Klapars A, Huang X, Buchwald SL. A general and efficient copper catalyst for the amidation of aryl halides. Journal of the American Chemical Society. 124: 7421-8. PMID 12071751 DOI: 10.1021/Ja0260465 |
0.631 |
|
| 2001 |
Torraca KE, Huang X, Parrish CA, Buchwald SL. An efficient intermolecular palladium-catalyzed synthesis of aryl ethers. Journal of the American Chemical Society. 123: 10770-1. PMID 11674023 DOI: 10.1021/Ja016863P |
0.73 |
|
| 2001 |
Huang X, Buchwald SL. New ammonia equivalents for the Pd-catalyzed amination of aryl halides. Organic Letters. 3: 3417-9. PMID 11594848 DOI: 10.1021/Ol0166808 |
0.639 |
|
| 2001 |
Klapars A, Antilla JC, Huang X, Buchwald SL. A general and efficient copper catalyst for the amidation of aryl halides and the N-arylation of nitrogen heterocycles. Journal of the American Chemical Society. 123: 7727-9. PMID 11481007 DOI: 10.1021/Ja016226Z |
0.718 |
|
| 2000 |
Fox JM, Huang X, Chieffi A, Buchwald SL. Highly active and selective catalysts for the formation of α-aryl ketones Journal of the American Chemical Society. 122: 1360-1370. DOI: 10.1021/Ja993912D |
0.709 |
|
| Show low-probability matches. |