Zobrazeno 1 - 10
of 148
pro vyhledávání: '"Kwang-Hyun Ahn"'
Autor:
A. Young Ji, Annaram Thirupathi, Joon Young Hwang, Yuri Kim, Gyuri Han, Kwang-Hyun Ahn, Kyungtae Kang, Eun Joo Kang
Publikováno v:
Organic Letters. 25:1541-1546
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30585635bf22505a76d88c3d09570e07
https://doi.org/10.1021/acs.orglett.3c00330
https://doi.org/10.1021/acs.orglett.3c00330
Publikováno v:
Bulletin of the Korean Chemical Society. 44:370-379
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4e46c5a2f6a192ebbae6fd232c18993
https://doi.org/10.1002/bkcs.12667
https://doi.org/10.1002/bkcs.12667
Publikováno v:
Molecules, Vol 25, Iss 3, p 522 (2020)
5,6-Dihydroergosterol-glucose is an organic synthetic derivative of spinasterol-glucose, which has potent anti-inflammatory activity. We previously synthesized alpha and beta anomers of DHE-glycosides and compared their inhibitory activity on CCL17 a
Externí odkaz:
https://doaj.org/article/3e78281d3adf44d1a5557f1bfaf2a3f1
Autor:
Yu Jeong, Jang, Hyeju, An, Seunghee, Choi, Jayeon, Hong, Seung Hyun, Lee, Kwang-Hyun, Ahn, Youngmin, You, Eun Joo, Kang
Publikováno v:
Organic letters. 24(24)
Green-light-driven Fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e464866b978ae1bebe86a218bac223eb
https://pubmed.ncbi.nlm.nih.gov/35687841
https://pubmed.ncbi.nlm.nih.gov/35687841
Publikováno v:
Journal of Materials Chemistry C. 9:12102-12110
Effective host materials are required to improve the performance of phosphorescent organic light-emitting diodes (PhOLEDs). Herein, a series of triazine-dibenzofuran-based n-type host materials, DBT1–DBT4, was prepared by varying the substitution p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52280f637088156d7ddbd45dc16a5940
https://doi.org/10.1039/d1tc01369f
https://doi.org/10.1039/d1tc01369f
Publikováno v:
The Journal of Organic Chemistry. 85:9727-9736
The controversial single-electron-transfer process, frequently proposed in many 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)-mediated reactions, was investigated experimentally and theoretically using the oxidative cyclization of aroylhydrazone wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc47e13c3f791694aaacbdaebe615398
https://doi.org/10.1021/acs.joc.0c00937
https://doi.org/10.1021/acs.joc.0c00937
Publikováno v:
Advanced Synthesis & Catalysis. 362:2183-2188
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc2b5de3fe7fb8a0a34f8b805e42356d
https://doi.org/10.1002/adsc.202000191
https://doi.org/10.1002/adsc.202000191
Publikováno v:
Journal of CO2 Utilization. 34:516-521
Novel, efficient and multifunctional binary systems consisting of Fe-bisiminopyridine complexes and additives are presented as effective catalysts for the synthesis of cyclic carbonates from epoxides and carbon dioxide. Due to the synergistic effects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22f1702c7a52abf388e922278194c69f
https://doi.org/10.1016/j.jcou.2019.07.033
https://doi.org/10.1016/j.jcou.2019.07.033
Publikováno v:
ChemSusChem. 12:409-415
The use of multifunctional and sustainable Fe catalysts for the formation of cyclic carbonates from epoxides and carbon dioxide at 80 °C and 3 bar pressure is presented. The optimal catalyst possesses a halide counteranion and a hydrogen bond donor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61184b880ce20be56c4da18b5b80902a
https://doi.org/10.1002/cssc.201802563
https://doi.org/10.1002/cssc.201802563
Publikováno v:
The Journal of organic chemistry. 85(15)
The controversial single-electron-transfer process, frequently proposed in many 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)-mediated reactions, was investigated experimentally and theoretically using the oxidative cyclization of aroylhydrazone wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2cd8ddf8ce538ec0d4f4061d6625ff66
https://pubmed.ncbi.nlm.nih.gov/32614179
https://pubmed.ncbi.nlm.nih.gov/32614179