Year |
Citation |
Score |
2023 |
Andrews JA, Kalepu J, Palmer CF, Poole DL, Christensen KE, Willis MC. Photocatalytic Carboxylate to Sulfinamide Switching Delivers a Divergent Synthesis of Sulfonamides and Sulfonimidamides. Journal of the American Chemical Society. PMID 37738304 DOI: 10.1021/jacs.3c07974 |
0.512 |
|
2022 |
Kanchupalli V, Thorbole LA, Kalepu J, Joseph D, Arshad M, Katukojvala S. Rhodium-Catalyzed Enal Transfer with -Methoxypyridazinium Salts. Organic Letters. 24: 3850-3854. PMID 35587254 DOI: 10.1021/acs.orglett.2c01424 |
0.529 |
|
2021 |
Moseley DF, Kalepu J, Willis MC. Azine-N-oxides as effective controlling groups for Rh-catalysed intermolecular alkyne hydroacylation. Chemical Science. 12: 13068-13073. PMID 34745537 DOI: 10.1039/d1sc03915f |
0.458 |
|
2019 |
Kalepu J, Pilarski LT. Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations. Molecules (Basel, Switzerland). 24. PMID 30813564 DOI: 10.3390/molecules24050830 |
0.346 |
|
2018 |
Kalepu J, Gandeepan P, Ackermann L, Pilarski LT. C4-H indole functionalisation: precedent and prospects. Chemical Science. 9: 4203-4216. PMID 29780550 DOI: 10.1039/C7Sc05336C |
0.322 |
|
2016 |
Dawande SG, Harode M, Kalepu J, Katukojvala S. Ag(i)-catalyzed intramolecular transannulation of enynone tethered donor-acceptor cyclopropanes: a new synthesis of 2,3-dihydronaphtho[1,2-b]furans. Chemical Communications (Cambridge, England). 52: 13699-13701. PMID 27819079 DOI: 10.1039/C6Cc07220H |
0.619 |
|
2016 |
Kalepu J, Katukojvala S. Dienamine Activation of Diazoenals: Application to the Direct Synthesis of Functionalized 1,4-Oxazines. Angewandte Chemie (International Ed. in English). 55: 7831-5. PMID 26949079 DOI: 10.1002/Anie.201600878 |
0.822 |
|
2014 |
Dawande SG, Kanchupalli V, Kalepu J, Chennamsetti H, Lad BS, Katukojvala S. Rhodium enalcarbenoids: direct synthesis of indoles by rhodium(II)-catalyzed [4+2] benzannulation of pyrroles. Angewandte Chemie (International Ed. in English). 53: 4076-80. PMID 24590818 DOI: 10.1002/Anie.201400161 |
0.614 |
|
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