Year |
Citation |
Score |
2008 |
Altman RA, Anderson KW, Buchwald SL. Pyrrole-2-carboxylic acid as a ligand for the Cu-catalyzed reactions of primary anilines with aryl halides. The Journal of Organic Chemistry. 73: 5167-9. PMID 18543973 DOI: 10.1021/Jo8008676 |
0.685 |
|
2007 |
Jones CP, Anderson KW, Buchwald SL. Sequential Cu-catalyzed amidation-base-mediated camps cyclization: a two-step synthesis of 2-Aryl-4-quinolones from o-halophenones. The Journal of Organic Chemistry. 72: 7968-73. PMID 17850097 DOI: 10.1021/Jo701384N |
0.708 |
|
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 |
0.684 |
|
2006 |
Anderson KW, Tundel RE, Ikawa T, Altman RA, Buchwald SL. Monodentate phosphines provide highly active catalysts for Pd-catalyzed C-N bond-forming reactions of heteroaromatic halides/amines and (H)N-heterocycles. Angewandte Chemie (International Ed. in English). 45: 6523-7. PMID 16955526 DOI: 10.1002/Anie.200601612 |
0.707 |
|
2006 |
Anderson KW, Ikawa T, Tundel RE, Buchwald SL. The selective reaction of aryl halides with KOH: synthesis of phenols, aromatic ethers, and benzofurans. Journal of the American Chemical Society. 128: 10694-5. PMID 16910660 DOI: 10.1021/Ja0639719 |
0.635 |
|
2006 |
Billingsley KL, Anderson KW, Buchwald SL. A highly active catalyst for Suzuki-Miyaura cross-coupling reactions of heteroaryl compounds. Angewandte Chemie (International Ed. in English). 45: 3484-8. PMID 16639772 DOI: 10.1002/Anie.200600493 |
0.703 |
|
2006 |
Tundel RE, Anderson KW, Buchwald SL. Expedited palladium-catalyzed amination of aryl nonaflates through the use of microwave-irradiation and soluble organic amine bases. The Journal of Organic Chemistry. 71: 430-3. PMID 16388678 DOI: 10.1021/Jo052131U |
0.629 |
|
2006 |
Larsen CH, Anderson KW, Tundel RE, Buchwald SL. Palladium-catalyzed Heck alkynylation of benzyl chlorides Synlett. 2941-2946. DOI: 10.1055/S-2006-949625 |
0.716 |
|
2006 |
Buchwald S, Anderson K, Ikawa T, Tundel R. Pd-Catalyzed Synthesis of Phenols and Aromatic Ethers from Aryl Halides Synfacts. 2006: 1163-1163. DOI: 10.1055/S-2006-949484 |
0.502 |
|
2005 |
Anderson KW, Buchwald SL. General catalysts for the Suzuki-Miyaura and Sonogashira coupling reactions of aryl chlorides and for the coupling of challenging substrate combinations in water. Angewandte Chemie (International Ed. in English). 44: 6173-7. PMID 16097019 DOI: 10.1002/Anie.200502017 |
0.58 |
|
2004 |
Klapars A, Parris S, Anderson KW, Buchwald SL. Synthesis of medium ring nitrogen heterocycles via a tandem copper-catalyzed C-N bond formation-ring-expansion process. Journal of the American Chemical Society. 126: 3529-33. PMID 15025480 DOI: 10.1021/Ja038565T |
0.563 |
|
2003 |
Anderson KW, Mendez-Perez M, Priego J, Buchwald SL. Palladium-catalyzed amination of aryl nonaflates. The Journal of Organic Chemistry. 68: 9563-73. PMID 14656080 DOI: 10.1021/Jo034962A |
0.651 |
|
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 |
0.685 |
|
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 |
0.653 |
|
2002 |
Anderson KW, Tepe JJ. The first intermolecular Friedel-Crafts acylation with beta-lactams. Organic Letters. 4: 459-61. PMID 11820904 DOI: 10.1021/Ol010291W |
0.321 |
|
2002 |
Anderson KW, Tepe JJ. Trifluoromethanesulfonic acid catalyzed Friedel-Crafts acylation of aromatics with β-lactams Tetrahedron. 58: 8475-8481. DOI: 10.1016/S0040-4020(02)01026-8 |
0.385 |
|
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