Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hyo Sang Yoon"'
Publikováno v:
Journal of the Korean Society for Aeronautical & Space Sciences. 51:253-261
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03c88887a5b399b2253a9b2635ecf332
https://doi.org/10.5139/jksas.2023.51.4.253
https://doi.org/10.5139/jksas.2023.51.4.253
Autor:
Jin Hong Lee, Jung Bok Ryu, Wonjun Na, Wan Joo Kim, Albert S. Lee, Hyo Sang Yoon, Chong Min Koo
Publikováno v:
Electrochimica Acta. 222:1847-1852
A series of ionic liquids containing imidazolium, pyrrolidinium, or ether-functionalized pyrrolidinium cations incorporated with the same counter anion of bis(fluorosulfonyl)imide (FSI − ) were synthesized to investigate the effects of the cation s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6d48ae28bdc29a5b12c4d2697f13682
https://doi.org/10.1016/j.electacta.2016.11.176
https://doi.org/10.1016/j.electacta.2016.11.176
Publikováno v:
Organic Letters. 14:3272-3275
A remarkably efficient photosensitizer, N719 dye, was used in asymmetric tandem Michael addition/oxyamination of aldehydes, rendering α,β-substituted aldehydes in good yields with excellent levels of enantioselectivity and diastereoselectivity. Thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cadef8ee27b258445366d2ba854a86b0
https://doi.org/10.1021/ol3011858
https://doi.org/10.1021/ol3011858
Publikováno v:
European Journal of Organic Chemistry. 2012:1901-1905
Platinum-catalyzed addition of the oxygen nucleophile of a carbamate to an allyl bromide was carried out to afford a range of biologically active 5-vinyl-substituted oxazolidinones in good yields. Over the course of the reaction, a platinum complex,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cec66293db55e12c5ae59739eb25465
https://doi.org/10.1002/ejoc.201101799
https://doi.org/10.1002/ejoc.201101799
Publikováno v:
European Journal of Organic Chemistry. 2011:3748-3754
Upon platinum-catalyzed hydrogenation, allenynes underwent reductive cyclization to provide hetero- and carbocycles with completely controlled regio- and stereoselectivity. By employing hydrogen as a reductant, the use of stoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::299947cad4c90523c368fd2b1b9c04e6
https://doi.org/10.1002/ejoc.201100280
https://doi.org/10.1002/ejoc.201100280
Publikováno v:
Bulletin of the Korean Chemical Society. 32:3117-3119
E-mail: hyjang2@ajou.ac.krReceived January 10, 2011, Accepted February 11, 2011Key Words : Hydrogenative cyclization, Bisallene, Hydrometallation, Platinum hydrideThe transition metal-catalyzed reaction of allenes hasemerged as a useful protocol to p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20dcb975b661c636d0eeabf2410db8ec
https://doi.org/10.5012/bkcs.2011.32.8.3117
https://doi.org/10.5012/bkcs.2011.32.8.3117
Autor:
Pilsoo Kim, Hye-Young Jang, Ju-Hye Kim, Xuan-Huong Ho, Hoseop Yun, Eun-Jin Park, Hyo-Sang Yoon, Hwa-Jung Lee
Publikováno v:
ChemInform. 44
The title reaction proceeds through iminium-catalyzed Michael addition followed by copper-assisted addition of TEMPO in a one-pot manner.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30e3080313778b5613bdf8d7d37a1bbf
https://doi.org/10.1002/chin.201348084
https://doi.org/10.1002/chin.201348084
Publikováno v:
ChemInform. 43
Platinum-catalyzed addition of the oxygen nucleophile of a carbamate to an allyl bromide was carried out to afford a range of biologically active 5-vinyl-substituted oxazolidinones in good yields. Over the course of the reaction, a platinum complex,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4595223bdb139a6a6d66cd6d90518b12
https://doi.org/10.1002/chin.201235131
https://doi.org/10.1002/chin.201235131
Publikováno v:
ChemInform. 42
The platinum-catalyzed reductive cyclization of allenynes provides hetero- and carbocycles with completely controlled regio- and stereoselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93980c0a1ac7c024c9ddb1a6e699dd5a
https://doi.org/10.1002/chin.201149108
https://doi.org/10.1002/chin.201149108