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Organic Chemistry: Current Research

Organic Chemistry: Current Research
Open Access

ISSN: 2161-0401

+44 20 3868 9735

Organic Chemistry: Current Research : Citations & Metrics Report

Articles published in Organic Chemistry: Current Research have been cited by esteemed scholars and scientists all around the world. Organic Chemistry: Current Research has got h-index 11, which means every article in Organic Chemistry: Current Research has got 11 average citations.

Following are the list of articles that have cited the articles published in Organic Chemistry: Current Research.

  2021 2020 2019 2018 2017

Year wise published articles

57 12 10 11 9

Year wise citations received

87 78 72 44 44
Journal total citations count 453
Journal impact factor 3.81
Journal 5 years impact factor 4.92
Journal cite score 5.93
Journal h-index 11
Journal h-index since 2017 10
Important citations

nishiya n, murai m, hosoda a, yonezawa h, omori n. bucillamine prevents afatinib-mediated inhibition of epidermal growth factor receptor signaling. pharmaceuticals. 2019;12(4):165.

sravya i. res rev: j pharm toxicol studies.

kolyakina ev, grishin id, gruzdeva ln, grishin df. polymerization of methyl methacrylate and acrylonitrile in the presence of copper bian complex. iran polym j. 2018;27(8):599-609.

chmielarz p. synthesis of pyridoxine‐based eagle‐shaped asymmetric star polymers through se atrp. polym advan technol. 2017;28(12):1787-1793.

chmielarz p. synthesis of inositol‐based star polymers through low ppm atrp methods. polymers for advanced technologies. 2017;28(12):1804-1812.

kohzadian a, zare a. effective and rapid synthesis of pyrido [2, 3-d: 6, 5-d′] dipyrimidines catalyzed by a mesoporous recoverable silica-based nanomaterial. silicon. 2019:1-9.

pal s, metin o, türkmen ye. synthesis of fluoranthene derivatives via tandem suzuki–miyaura and intramolecular c–h arylation reactions under both homogeneous and heterogeneous catalytic conditions. acs omega. 2017;2(12):8689-8696.

vekteris v, styra a, mokšin v, grinbergienÄ— i, jurevičius m, turla v, et al. numerical simulation of a pulsating flow generated in an ejector. transactions of famena. 2018;42(2):97-107.

koe a. copper-catalyzed one-pot tandem synthesis of unsymmetrical diaryl chalcogenides. western illinois university; 2015.

Åžoriga Åžg, costinela i. interaction of diphenylamine (dpa) with cu2o (110) and (111) surfaces.

pagett ab, lloyd‐jones gc. suzuki–miyaura cross‐coupling. org reac. 2004:547-620.

chopade mu, magar rr, choudhare ss, padghan sv. development of drug intermediates via alkylation using fe (acac) 3 as transition metal catalyst.

lee d, kondo h, kuwayama y, takahashi k, arima s, omura s, et al. total synthesis of 4-epi-atpenin a5 as a potent nematode complex ii inhibitor. tetrahedron. 2019;75(24):3178-3185.

kolanowska a, kuziel aw, jÄ™drysiak rg, krzywiecki m, korczeniewski e, wiÅ›niewski m, et al. ullmann reactions of carbon nanotubes—advantageous and unexplored functionalization toward tunable surface chemistry. nanomaterials. 2019;9(11):1619.

mitsudo k, asada t, inada t, kurimoto y, mandai h, suga s. cu/fe/o= pph3-catalyzed etherification for the synthesis of aryl 3-benzo [b] thienyl ethers. chem lett. 2018;47(8):1044-1047.

onoabedje ea, okoro uc. ligand-supported palladium-catalyzed cross-coupling reactions of (hetero) aryl chlorides. syn comm. 2019;49(17):2117-2146.

layek s, agrahari b, dey s, ganguly r, pathak dd. copper (ii)-faciliated synthesis of substituted thioethers and 5-substituted 1h-tetrazoles: experimental and theoretical studies. j organomet chem. 2019;896:194-206.

pankhurst jr, curcio m, sproules s, lloyd-jones gc, love jb. earth-abundant mixed-metal catalysts for hydrocarbon oxygenation. inorganic chemistry. 2018;57(10):5915-5928.

kazemi n, shahri mm. magnetically separable and reusable cufe 2 o 4 spinel nanocatalyst for the o-arylation of phenol with aryl halide under ligand-free condition. j inorg organomet p. 2017;27(5):1264-1273.

gupta a, jamatia r, patil ra, ma yr, pal ak. copper oxide/reduced graphene oxide nanocomposite-catalyzed synthesis of flavanones and flavanones with triazole hybrid molecules in one pot: a green and sustainable approach. acs omega. 2018;3(7):7288-7299.

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