Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Jaeduk Yoo"'
Autor:
Kang Min Ok, Ranjan Dutta, Dikhi Firmansyah, Jaeduk Yoo, Hongil Jo, Chang-Hee Lee, Endale Mulugeta, Ravi Ranjan Kumar
Publikováno v:
Bulletin of the Korean Chemical Society. 38:1163-1168
A series of carbazole–benzimidazole conjugates and corresponding BF2-complexes (BODIPYs) are synthesized and characterized. Carbazole–benzimidazole conjugates are synthesized by the condensation of 1-formyl carbazole and phenylene diamines in goo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba46bdee3f4266bc01d99106037d327b
https://doi.org/10.1002/bkcs.11240
https://doi.org/10.1002/bkcs.11240
Autor:
Eli M. Espinoza, Chang-Hee Lee, Valentine I. Vullev, Daniel T. Gryko, Kamil Skonieczny, Jillian M. Larsen, Jaeduk Yoo, Michał Barbasiewicz
Publikováno v:
Chemistry – A European Journal. 22:7485-7496
Photoinduced intramolecular direct arylation allows structurally unique compounds containing phenanthro[9',10':4,5]imidazo[1,2-f]phenanthridine and imidazo[1,2-f]phenanthridine skeletons, which mediate excited-state intramolecular proton transfer (ES
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6755ae581c24587d964c1d9953bb45a1
https://doi.org/10.1002/chem.201504944
https://doi.org/10.1002/chem.201504944
Publikováno v:
Bulletin of the Korean Chemical Society. 36:1919-1921
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1095a2039184058cd4b46d2edde6fef0
https://doi.org/10.1002/bkcs.10352
https://doi.org/10.1002/bkcs.10352
Autor:
Jungyeol Lee, Krishna Kanta Ghosh, Dohee Kim, Nam-Young Kang, Jun-Young Kim, Jaeduk Yoo, Wan Si Yan Diana, Yun Kyung Kim, Yun-Mi Jeong, Young-Tae Chang
Publikováno v:
Chemical Communications. 51:9336-9338
A low-toxicity nucleus staining fluorescent probe, CDb12, was developed for real time mitosis imaging in live cells. CDb12 was identified by unbiased high-throughput imaging-based screening of a new xanthone library (AX). Unlike the conventional Hoec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ee1e4040d584ac1b982a2f91d3104d7
https://doi.org/10.1039/c5cc02295a
https://doi.org/10.1039/c5cc02295a
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 15:674-677
meso-diethylmalonylidene-(1,4-naphthi)thiaporphyrin containing exocyclic C – C double bonds at meso-positions has been synthesized and characterized. The compound undergoes initial protonation at the α-position of the diethylmalonyl group with lar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b95e5a7c129fa43e3f3498724b3fc90
https://doi.org/10.1142/s1088424611003604
https://doi.org/10.1142/s1088424611003604
Autor:
Jung Oh Huh, Chang-Hee Lee, Hyosun Lee, Yoon Sup Lee, June Jeon, Kibong Kim, Jong Taek Kim, Jaeduk Yoo, David G. Churchill, Shin Hei Choi
Publikováno v:
Inorganic Chemistry. 50:5351-5360
One 8-phenyl and two 8-mesityl-substituted "scorpionate"-like BODIPY-type species of the formula [3,4,4-tris(5-R-(2-thienyl))-8-(2,4,6-R'-phenyl)-4-bora-3a,4a-diaza-s-indacene (R = H, R' = H, 3a; R, = H, R' = Me, 2a; R, = Me, R' = Me, 2b)] have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2d036e3c1edd55537b0e21fa6ffb59d
https://doi.org/10.1021/ic101681h
https://doi.org/10.1021/ic101681h
Publikováno v:
European Journal of Organic Chemistry. 2011:2911-2915
A supramolecular host-guest complex stimulated by lithium cation and fluoride anion, functioning as reliable fluorescence "Off-On-Off" switching system has been developed. Nonfluorescent, receptor-bound fluorophore is exclusively displaced by second
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2ab735b34ff2ba912cd0a7f5755b745
https://doi.org/10.1002/ejoc.201100359
https://doi.org/10.1002/ejoc.201100359
Publikováno v:
Bulletin of the Korean Chemical Society. 31:630-634
The design and synthesis of anion receptors possessing high affinity and selectivity still remains a challenging task due to rather complex nature of anionic species compared with those of cations. Among the vari-ous neutral anion receptors reported
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82f9543d3c58f4383370a50769c59b33
https://doi.org/10.5012/bkcs.2010.31.03.630
https://doi.org/10.5012/bkcs.2010.31.03.630
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 66:209-212
Pyrrole-based tripodal receptors have been synthesized and characterized. The synthesis utilized an unusual direct nucleophilic substitution of tris-(bromomethyl)-2,4,6-trimethybenzene with pyrrole. The anion binding studies indicate that the acetate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c4a20be29699dae6dda4bc0fea5ee54
https://doi.org/10.1007/s10847-009-9700-0
https://doi.org/10.1007/s10847-009-9700-0
Publikováno v:
Organic Letters. 11:3626-3629
A strapped calix[4]pyrrole bearing a 1,3-indanedione group at a beta-pyrrolic position has been synthesized and studied as a ratiometric cyanide-selective chemosensor. A concentration-dependent bleaching of the initial yellow color was observed upon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d74f4cb2307728985606b101b2211e5
https://doi.org/10.1021/ol901361h
https://doi.org/10.1021/ol901361h