Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Ye Lim Kim"'
Autor:
Jee Young Seo, Hye-Ryeong Jo, Seung Hoon Lee, Do Gyeong Kim, Huiju Lee, Ye Lim Kim, Young In Choi, Sung Jun Jung, Hyeon Son
Publikováno v:
iScience, Vol 27, Iss 1, Pp 108617- (2024)
Summary: To investigate whether the defects in transient receptor potential canonical 4 (TRPC4), which is strongly expressed in the hippocampus, are implicated in ASD, we examined the social behaviors of mice in which Trpc4 was deleted (Trpc4−/−)
Externí odkaz:
https://doaj.org/article/c31a904f9c3d4e7aaefc593b5ba9f8d3
Publikováno v:
Fermentation, Vol 9, Iss 7, p 612 (2023)
Lactic acid bacteria have become popular because of their γ-aminobutyric acid (GABA)-producing ability. In the present study, we selected four Levilactobacillus brevis strains (MG5552, MG5405, MG5261, and MG5522) with GABA-producing ability from the
Externí odkaz:
https://doaj.org/article/1f3d98768f89425fbaf2a9e47a7faff6
Rh(II)-Catalyzed C–N Bond Formation Using Enynones and N–H Imines: An Approach to Diarylmethylamines
Publikováno v:
The Journal of Organic Chemistry. 87:16424-16435
A Rh(II)-catalyzed furyl carbene N-H insertion reaction involving an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9162642528473aad2893d0186ecac69b
https://doi.org/10.1021/acs.joc.2c02119
https://doi.org/10.1021/acs.joc.2c02119
Autor:
Ye Lim Kim, Jung Hyun Chae
Publikováno v:
Family and Environment Research. 60:331-344
The purpose of this study was to identify a support method for the introduction of metaverse-based classes (MBC) in home economics (HE) education. This was achieved by diagnosing the stages of concern and levels of use exhibited by HE teachers applyi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f2a9b0b95d3a90907efe7bf9e850d7a
https://doi.org/10.6115/fer.2022.022
https://doi.org/10.6115/fer.2022.022
Publikováno v:
Journal & Article Management System. 44:179-199
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f1051b0ebcae40f01e7c1c8e7a82e7d
https://doi.org/10.31927/asec.17.4.10
https://doi.org/10.31927/asec.17.4.10
Publikováno v:
Organic Letters. 23:6674-6679
An atom-economical strategy for the C-H alkenylation and C-H allylation of arenes by employing cyclopropenes as versatile alkenylating and allylating reagents is reported, catalyzed by cobalt. The Co-catalyzed C-H alkenylation process involves sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d0d84bea87f04c918f2479cef664a50
https://doi.org/10.1021/acs.orglett.1c02219
https://doi.org/10.1021/acs.orglett.1c02219
Publikováno v:
European Journal of Organic Chemistry. 2020:4026-4030
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12b1a64518f778e719bfad05f059c7e7
https://doi.org/10.1002/ejoc.202000565
https://doi.org/10.1002/ejoc.202000565
Autor:
Hyewon Chang, Ye-Lim Kim
Publikováno v:
School Mathematics. 22:51-68
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::616b7ab46a4fdb33ec7d7af684e97e4f
https://doi.org/10.29275/sm.2020.03.22.1.51
https://doi.org/10.29275/sm.2020.03.22.1.51
Publikováno v:
The Journal of organic chemistry. 86(23)
A simple transition metal-free strategy for the synthesis of pyrido[1,2-a]indolone derivatives has been devised through sodium methoxide-catalyzed intramolecular cyclization of 2-alkenylated N-pyrimidyl indoles. The reactions involved a Smiles rearra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8435fd03615021434585a5f4e1b85c61
https://pubmed.ncbi.nlm.nih.gov/34761671
https://pubmed.ncbi.nlm.nih.gov/34761671
Publikováno v:
Organic letters. 23(17)
An atom-economical strategy for the C-H alkenylation and C-H allylation of arenes by employing cyclopropenes as versatile alkenylating and allylating reagents is reported, catalyzed by cobalt. The Co-catalyzed C-H alkenylation process involves sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::01c67c02a8c7ae53123420e5bea62e56
https://pubmed.ncbi.nlm.nih.gov/34474571
https://pubmed.ncbi.nlm.nih.gov/34474571