Year |
Citation |
Score |
2020 |
Renner J, Thakur A, Rutz PM, Cowley JM, Evangelista JL, Kumar P, Prater MB, Stolley RM, Louie J. Total Synthesis of Indolizidine Alkaloids via Nickel-Catalyzed (4 + 2) Cyclization. Organic Letters. PMID 31928010 DOI: 10.1021/Acs.Orglett.9B04479 |
0.684 |
|
2020 |
Chandra D, Verma S, Pandey CB, Yadav AK, Kumar P, Tiwari B, Jat JL. Direct synthesis of secondary amides from ketones through Beckmann rearrangement using O-(mesitylsulfonyl)hydroxylamine Tetrahedron Letters. 61: 151822. DOI: 10.1016/J.Tetlet.2020.151822 |
0.341 |
|
2015 |
Thakur A, Evangelista JL, Kumar P, Louie J. An in Situ Approach to Nickel-Catalyzed Cycloaddition of Alkynes and 3-Azetidinones. The Journal of Organic Chemistry. PMID 26412483 DOI: 10.1021/Acs.Joc.5B01458 |
0.679 |
|
2014 |
Kumar P, Thakur A, Hong X, Houk KN, Louie J. Ni(NHC)]-catalyzed cycloaddition of diynes and tropone: apparent enone cycloaddition involving an 8π insertion. Journal of the American Chemical Society. 136: 17844-51. PMID 25416006 DOI: 10.1021/Ja5105206 |
0.662 |
|
2012 |
Kumar P, Zhang K, Louie J. An expeditious route to eight-membered heterocycles by nickel-catalyzed cycloaddition: Low-temperature Csp2-Csp3 bond cleavage Angewandte Chemie - International Edition. 51: 8602-8606. PMID 22806996 DOI: 10.1002/Anie.201203521 |
0.646 |
|
2012 |
Kumar P, Louie J. A single step approach to piperidines via Ni-catalyzed β-carbon elimination. Organic Letters. 14: 2026-9. PMID 22468962 DOI: 10.1021/Ol300534J |
0.67 |
|
2011 |
Kumar P, Louie J. Nickel-mediated cycloaddition by two sequential C-H activations. Angewandte Chemie (International Ed. in English). 50: 10768-9. PMID 21954038 DOI: 10.1002/Anie.201103621 |
0.507 |
|
2011 |
Kumar P, Prescher S, Louie J. A serendipitous discovery: nickel catalyst for the cycloaddition of diynes with unactivated nitriles. Angewandte Chemie (International Ed. in English). 50: 10694-8. PMID 21932226 DOI: 10.1002/Anie.201104475 |
0.636 |
|
2011 |
Kumar P, Troast DM, Cella R, Louie J. Ni-catalyzed ketene cycloaddition: a system that resists the formation of decarbonylation side products. Journal of the American Chemical Society. 133: 7719-21. PMID 21528904 DOI: 10.1021/Ja2007627 |
0.58 |
|
2011 |
Kumar P, Louie J. Nickel-katalysierte Cycloaddition durch zwei sequenzielle C-H-Aktivierungen Angewandte Chemie. 123: 10956-10958. DOI: 10.1002/Ange.201103621 |
0.498 |
|
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