Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Huan Chang Hsiao"'
Autor:
Cheng-Ming Hsieh, Huan-Chang Hsiao, Yuto Yamada, Wei-Ru Wu, U-Ser Jeng, Chun-Jen Su, Ying-Sheng Lin, Michihisa Murata, Yuan Jay Chang, Shih-Ching Chuang
Publikováno v:
ACS Applied Materials & Interfaces. 14:39109-39119
The device efficiency of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55d99fef9a295d7c2c66a188625cb675
https://doi.org/10.1021/acsami.2c06354
https://doi.org/10.1021/acsami.2c06354
Publikováno v:
Journal of the Chinese Chemical Society.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df534d971bd9f6b572ea6f619465a51d
https://doi.org/10.1002/jccs.202300145
https://doi.org/10.1002/jccs.202300145
Publikováno v:
Acta Crystallographica Section E Crystallographic Communications. 78:590-593
The crystal of the title compound, C60H38N2O2, which crystallizes in the monoclinic space group P21/n, was obtained by thermal evaporation of a 1:1 dichloromethane and hexanes solution of the pure compound. The crystal structure is stabilized by π
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ed27c480e329d3c4b954ee92bcf2f62
https://doi.org/10.1107/s2056989022004509
https://doi.org/10.1107/s2056989022004509
Autor:
Pratheepkumar Annamalai, Shang You Sun, Huan Chang Hsiao, Shih Ching Chuang, Jayachandran Jayakumar
Publikováno v:
Advanced Synthesis & Catalysis. 363:1695-1701
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46891bd6fb58b654e35e53c324f22db6
https://doi.org/10.1002/adsc.202001404
https://doi.org/10.1002/adsc.202001404
Publikováno v:
Organic Letters. 22:6252-6256
A novel and efficient reductive N-alkenylation of iminoquinones with electron-deficient olefins has been successfully developed by Pd(II)-catalyzed redox-neutral reactions, which provides a synthes...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfe4bd674379c1e1b8e666bcb2a3b9d4
https://doi.org/10.1021/acs.orglett.0c01929
https://doi.org/10.1021/acs.orglett.0c01929
Publikováno v:
Journal of the Chinese Chemical Society. 67:430-436
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d14a3b4949ed8cf5ac3864b9ccddb6b5
https://doi.org/10.1002/jccs.201900462
https://doi.org/10.1002/jccs.201900462
Publikováno v:
Acta crystallographica. Section E, Crystallographic communications. 78(Pt 6)
The crystal of the title compound, C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::de9a8909365bae6f88df3e5d9121a176
https://pubmed.ncbi.nlm.nih.gov/36072156
https://pubmed.ncbi.nlm.nih.gov/36072156
Autor:
Huan-Chang Hsiao, Shih-Ching Chuang, Jayachandran Jayakumar, Shang-You Sun, Guganchandar Vedarethinam
Publikováno v:
Angewandte Chemie. 132:699-704
Quaternary ammonium salts were synthesized in moderate to good yields through double oxidative C-H bond activation on azobenzenes. The mechanism of the highly regioselective reaction of 2-azobiaryls with alkenes to give orange-red-fluorescent cinnoli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92c3be5570b6c5ed8de3e2a658f73ea4
https://doi.org/10.1002/ange.201910959
https://doi.org/10.1002/ange.201910959
Publikováno v:
Advanced Synthesis & Catalysis. 361:683-689
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::103d4f280223e6b9ebfe5facedbe2ca4
https://doi.org/10.1002/adsc.201801352
https://doi.org/10.1002/adsc.201801352
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications; Jun2022, Vol. 78 Issue 6, p590-593, 14p