Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Yusuke Makida"'
Autor:
Sungho Nam, Ji Whan Kim, Hye Jin Bae, Yusuke Makida Maruyama, Daun Jeong, Joonghyuk Kim, Jong Soo Kim, Won‐Joon Son, Hyein Jeong, Jaesang Lee, Soo‐Ghang Ihn, Hyeonho Choi
Publikováno v:
Advanced Science, Vol 8, Iss 16, Pp n/a-n/a (2021)
Abstract Although the organic light‐emitting diode (OLED) has been successfully commercialized, the development of deep‐blue OLEDs with high efficiency and long lifetime remains a challenge. Here, a novel hyperfluorescent OLED that incorporates t
Externí odkaz:
https://doaj.org/article/1425e622608c4f4fa4064df44d26aeb4
Akademický článek
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Autor:
Young Mo Sung, Eun Suk Kwon, Yusuke Makida Maruyama, Youngsik Shin, Soo-Ghang Ihn, Jong Soo Kim, Hyeonho Choi, Hyo Sug Lee, Jung-Hwa Kim, Joonghyuk Kim, Soohwan Sul
Intramolecular charge transfer (ICT) plays a critical role in determining the photophysical properties of organic molecules, including their luminescence efficiencies. Twisted intramolecular charge transfer (TICT) is a process in which structural cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::435701e263cfdce2e2a9653b9b7cbe00
https://doi.org/10.21203/rs.3.rs-1134592/v1
https://doi.org/10.21203/rs.3.rs-1134592/v1
Akademický článek
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Publikováno v:
The Journal of Organic Chemistry. 83:3829-3839
A chemoselective hydrogenation of isoquinoline carbocycles was achieved by using the catalyst prepared from Ru(methallyl)2(cod) and trans-chelate chiral ligand PhTRAP. The unique chemoselectivity achieved in this hydrogenation could be ascribed to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86394013cddf10f8821991698c212436
https://doi.org/10.1021/acs.joc.8b00190
https://doi.org/10.1021/acs.joc.8b00190
Publikováno v:
Chemistry Letters. 46:1814-1817
A wide range of benzyl carbonates reacted with dimethyl phosphonate or diphenylphosphine oxide in the presence of the palladium catalyst, [Pd(η3-allyl)Cl]2–DPEphos, to give dimethyl benzylphosphonates and benzyldiphenylphosphine oxides in high yie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc6cf4d9735b55f5ec50a40e4fb237a9
https://doi.org/10.1246/cl.170901
https://doi.org/10.1246/cl.170901
Autor:
Hye Jin Bae, Jaesang Lee, Ji Whan Kim, Sungho Nam, Jong Soo Kim, Hyeonho Choi, Yusuke Makida Maruyama, Hye-In Jeong, Daun Jeong, Joonghyuk Kim, Won-Joon Son, Soo-Ghang Ihn
Publikováno v:
Advanced Science
Advanced Science, Vol 8, Iss 16, Pp n/a-n/a (2021)
Advanced Science, Vol 8, Iss 16, Pp n/a-n/a (2021)
Although the organic light‐emitting diode (OLED) has been successfully commercialized, the development of deep‐blue OLEDs with high efficiency and long lifetime remains a challenge. Here, a novel hyperfluorescent OLED that incorporates the Pt(II)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0989a4522f33f086d122e7eeb51f3884
https://doi.org/10.1002/advs.202100586
https://doi.org/10.1002/advs.202100586
Autor:
Ryoichi Kuwano, Yusuke Makida
The dearomative reduction of (hetero)aromatic compounds represents one of straightforward and attractive transformations for the construction of chiral cyclic compounds, which contain important structural motifs in a wide range of scientific discipli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65510c31e58dfc623e4f4e98a44078cd
https://doi.org/10.1016/b978-0-12-812126-9.00005-5
https://doi.org/10.1016/b978-0-12-812126-9.00005-5
Publikováno v:
Angewandte Chemie International Edition. 55:11859-11862
High enantioselectivity was achieved for the hydrogenation of azaindoles by using the chiral catalyst, which was prepared from [Ru(η(3) -methallyl)2 (cod)] and a trans-chelating bis(phosphine) ligand (PhTRAP). The dearomative reaction exclusively oc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b7a4f7a5f24ad29d184e62875dd9239
https://doi.org/10.1002/anie.201606083
https://doi.org/10.1002/anie.201606083
Vicinal stereocenters are found in many natural and unnatural compounds. Although metal-catalyzed cross-coupling reactions of unactivated alkyl electrophiles are emerging as a powerful tool in organic synthesis, there have been virtually no reports o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::491e05aaea90ecdf33ab2f69ac72845d
https://resolver.caltech.edu/CaltechAUTHORS:20170419-135029412
https://resolver.caltech.edu/CaltechAUTHORS:20170419-135029412