Year |
Citation |
Score |
2020 |
Zhang CY, Flor S, Ruiz P, Dhakal R, Hu X, Teesch LM, Ludewig G, Lehmler HJ. 3,3'-Dichlorobiphenyl is Metabolized to a Complex Mixture of Oxidative Metabolites, Including Novel Methoxylated Metabolites, by HepG2 Cells. Environmental Science & Technology. PMID 32910851 DOI: 10.1021/Acs.Est.0C03476 |
0.478 |
|
2020 |
Elser BA, Kayali K, Dhakal R, O'Hare B, Wang K, Lehmler HJ, Stevens HE. Combined maternal exposure to cypermethrin and stress affect embryonic brain and placental outcomes in mice. Toxicological Sciences : An Official Journal of the Society of Toxicology. PMID 32191333 DOI: 10.1093/Toxsci/Kfaa040 |
0.434 |
|
2019 |
Dhakal R, Parkin S, Lehmler HJ. 3-(3,5-Dichlorophenyl)benzene-1,2-diol. Iucrdata. 4. PMID 34708161 DOI: 10.1107/s2414314619012021 |
0.49 |
|
2019 |
Dhakal R, Parkin S, Lehmler HJ. 2,3-Dichloro-3',4'-dihydroxybiphenyl. Iucrdata. 4. PMID 32030359 DOI: 10.1107/S241431461900662X |
0.54 |
|
2019 |
Dhakal R, Parkin S, Lehmler HJ. 3,5-Dichloro-3',4'-dimethoxybiphenyl. Iucrdata. 4. PMID 32030358 DOI: 10.1107/S2414314619005182 |
0.515 |
|
2019 |
Dhakal R, Li X, Parkin SR, Lehmler HJ. Synthesis of mono- and dimethoxylated polychlorinated biphenyl derivatives starting from fluoroarene derivatives. Environmental Science and Pollution Research International. PMID 31893358 DOI: 10.1007/S11356-019-07133-3 |
0.567 |
|
2019 |
Saktrakulkla P, Dhakal RC, Lehmler HJ, Hornbuckle KC. A semi-target analytical method for quantification of OH-PCBs in environmental samples. Environmental Science and Pollution Research International. PMID 31359319 DOI: 10.1007/S11356-019-05775-X |
0.472 |
|
2019 |
Dhakal R, Parkin S, Lehmler H. 3-(3,5-Dichlorophenyl)benzene-1,2-diol Iucrdata. 4. DOI: 10.1107/S2414314619012021 |
0.56 |
|
2018 |
Dhakal R, Ivancic M, Brewer M. Two-Step Sequence of Cycloadditions Gives Structurally Complex Tetracyclic 1,2,3,4-Tetrahydrocinnoline Products. The Journal of Organic Chemistry. PMID 29781614 DOI: 10.1021/Acs.Joc.8B00683 |
0.658 |
|
2016 |
Dhakal RC, Brewer M. Intramolecular (4 + 2) cycloaddition of aryl-1-aza-2-azoniaallene salts: A practical approach to highly sterically-congested polycyclic protonated azomethine imines. Tetrahedron. 72: 3718-3728. PMID 32071487 DOI: 10.1016/J.Tet.2016.03.037 |
0.677 |
|
2015 |
Hong X, Bercovici DA, Yang Z, Al-Bataineh N, Srinivasan R, Dhakal RC, Houk KN, Brewer M. Mechanism and Dynamics of Intramolecular C-H Insertion Reactions of 1-Aza-2-azoniaallene Salts. Journal of the American Chemical Society. 137: 9100-7. PMID 26151292 DOI: 10.1021/Jacs.5B04474 |
0.688 |
|
2015 |
Hong X, Bercovici DA, Yang Z, Al-Bataineh N, Srinivasan R, Dhakal RC, Houk KN, Brewer M. Mechanism and Dynamics of Intramolecular C-H Insertion Reactions of 1-Aza-2-azoniaallene Salts Journal of the American Chemical Society. 137: 9100-9107. DOI: 10.1021/jacs.5b04474 |
0.672 |
|
2015 |
Dhakal RC, Brewer M. Intramolecular (4+2) cycloaddition of aryl-1-aza-2-azoniaallene salts: A practical approach to highly sterically-congested polycyclic protonated azomethine imines Tetrahedron. DOI: 10.1016/j.tet.2016.03.037 |
0.677 |
|
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