Zobrazeno 1 - 10
of 58
pro vyhledávání: '"In-Sook Han Lee"'
Autor:
Youngran Na, Wi-Gyeong Gwon, Eun Ju Kim, Mee-ok Lee, Sohyun Park, Eun-hee Park, Hee-soo Koo, Byung-jun Kim, Su-Jeong Hwang, In-Sook Han Lee
Publikováno v:
Journal of Food Hygiene and Safety. 35:219-224
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7fae266bb3afd2cd9848fc014464c56
https://doi.org/10.13103/jfhs.2020.35.3.219
https://doi.org/10.13103/jfhs.2020.35.3.219
Autor:
In-Sook Han Lee, Eun Jeong Jeong
Publikováno v:
Bulletin of the Korean Chemical Society. 40:668-673
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::203f7266f26f5fed6fb2d905ce29cdb6
https://doi.org/10.1002/bkcs.11749
https://doi.org/10.1002/bkcs.11749
Publikováno v:
Journal of Industrial and Engineering Chemistry. 58:386-390
New Ir(III) compound with sky-blue phosphorescence has been synthesized by one-pot reaction of [Ir(COD)2]BF4 with 2,3-dimethylimidazo[1,2-f]phenanthridine. This complex has a facial(fac) geometry around iridium metal center. The ligand has been found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50aca07bede610ee18b1e27c2195c168
https://doi.org/10.1016/j.jiec.2017.09.052
https://doi.org/10.1016/j.jiec.2017.09.052
Autor:
Sungjae Yang, Jun Ho Kim, Yong Kim, In-Sook Han Lee, Eun Jeong Jeong, Young-Jin Son, Deok Jeong, Jae Youl Cho, Tae Woong Kim, Byong Chul Yoo, Sunggyu Kim
Publikováno v:
Biomolecules & Therapeutics
(E)-3-Phenyl-1-(2-pyrrolyl)-2-propenone (PPP) is a pyrrole derivative of chalcone, in which the B-ring of chalcone linked to β-carbon is replaced by pyrrole group. While pyrrole has been studied for possible Src inhibition activity, chalcone, especi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c999e03156f822320e3867a4bd141e17
http://europepmc.org/articles/PMC5098538
http://europepmc.org/articles/PMC5098538
Autor:
In-Sook Han Lee, Eun Jeong Jeong
Publikováno v:
Bulletin of the Korean Chemical Society. 37:538-543
The 1H and 13C chemical shifts and the mass spectral fragmentation patterns of 1-aryl-3-phenylpropanes with m- or p-substituents (H, NO2 , Br, Cl, OCH3 , CH3 ) were studied. The electronic effects of the substituents seemed to be transmitted by the t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4a778c175f2726e15e5f591d4b3c4c8
https://doi.org/10.1002/bkcs.10720
https://doi.org/10.1002/bkcs.10720
Autor:
Eun Jeong Jeong, In-Sook Han Lee
Publikováno v:
Bulletin of the Korean Chemical Society. 36:295-299
1H and 13C NMR spectra of aryl esters of propionic acid, acrylic acid, and propiolic acid were systematically examined to find out the substituent effect on the chemical shift. The values of the chemical shift of the carbonyl carbon showed an inverse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf6127fd4a0e71752e03bc98c08fdc4d
https://doi.org/10.1002/bkcs.10067
https://doi.org/10.1002/bkcs.10067
Publikováno v:
Journal of Physical Organic Chemistry. Jul2007, Vol. 20 Issue 7, p484-490. 7p. 3 Charts, 3 Graphs.
Publikováno v:
Bulletin of the Korean Chemical Society. 34:936-942
Department of Chemistry, Kangwon National University, Chuncheon 200-701, KoreaReceived December 13, 2012, Accepted March 2, 2013Series of (E)-1-aryl-3-(2-pyrrolyl)-2-propenones, that were aldol condensation products between pyrrole-2-carbaldehyde and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dda4c7d6790b0292e1de39e7e633590
https://doi.org/10.5012/bkcs.2013.34.3.936
https://doi.org/10.5012/bkcs.2013.34.3.936
Publikováno v:
Bulletin of the Korean Chemical Society. 31:1689-1694
Substituent chemical shifts were examined for the 2- and 3-thiophene derivatives of chalcone and compared to the thiophene series of derivatives with the phenyl series. The chemical shift values for the α-carbons of the enones showed and inverse cor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c115f45011748e24395ed42dfd43bfe0
https://doi.org/10.5012/bkcs.2010.31.6.1689
https://doi.org/10.5012/bkcs.2010.31.6.1689
Autor:
Hyun Joo Kil, In-Sook Han Lee
Publikováno v:
The Journal of Physical Chemistry A. 113:10704-10709
Primary kinetic isotope effects (KIEs), k(H)/k(D), have been determined spectrophotometrically for the reactions of NAD(+) analogues (acridinium ions, 1a-e(+), and quinolinium ion, 2(+)) with heteroaromatic compounds such as 3-methyl-2-phenylbenzothi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9a59e3d47435f65c52721b57d986de4
https://doi.org/10.1021/jp905937x
https://doi.org/10.1021/jp905937x