Ram Chandra Dhakal, Ph.D. - Publications

Affiliations: 
2001-2003 Chemistry/Biology Tri-Chandra Multiple Campus 
 2004-2005 Chemistry Tribhuvan University 
 2012-2013 Chemistry Middle Tennessee State University, Murfreesboro, TN, United States 
 2013-2017 Chemistry University of Vermont, Burlington, VT, United States 
Area:
organic synthesis, Organic Methodology, Medicinal Chemistry, Pharmaceutical Chemistry, Computational Chemistry, Natural Product, Heterocycles, Cycloaddition, Organometallic, Isolation and Extraction

13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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  0.64
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  0.64
2019 Dhakal R, Parkin S, Lehmler HJ. 2,3-Dichloro-3',4'-dihydroxybiphenyl. Iucrdata. 4. PMID 32030359 DOI: 10.1107/S241431461900662X  0.64
2019 Dhakal R, Parkin S, Lehmler HJ. 3,5-Dichloro-3',4'-dimethoxybiphenyl. Iucrdata. 4. PMID 32030358 DOI: 10.1107/S2414314619005182  0.64
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  0.64
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  0.64
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  1
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  1
2016 Dhakal, R. C., 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. DOI: http://doi.org/10.1016/j.tet.2016.03.037  0.8
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  1
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  1
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  1
2009 Ram Chandra Dhakal, Meena Rajbhandari, Surya K. Kalauni, Suresh Awale, Mohan. B. Gewali. Phytochemical Constituents of the Bark of Vitex negundo L. Journal of Nepal Chemical Society. 89-92. DOI: http://dx.doi.org/10.3126/jncs.v23i0.2101  0.01
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