Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Nian-Yu Huang"'
Publikováno v:
Chinese Chemical Letters. 27:345-348
A green Passerini three-component reaction of 2-(4-oxo-4,5,6,7-tetrahydro-1 H -indol-1-yl)acetic acid with alkyl or aryl isocyanides and aldehydes was reported under aqueous conditions at 35 °C for 1 h, and 21 indolone- N -amino acid derivatives wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64f7742956171664b6ce378145cc3fe9
https://doi.org/10.1016/j.cclet.2015.11.008
https://doi.org/10.1016/j.cclet.2015.11.008
Publikováno v:
Advanced Materials Research. 1096:477-480
Dye-sensitized solar cells are attracted much interest in the fields of clean energy. In this work, a novel ruthenium terpyridine dimeric complex (N749 dimer) was designed and synthesized through the coordination of 4,4',4"-tricarboxy-2,2':6',2"-terp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa4d34a0008bdedd9ccdd37dfbb9d439
https://doi.org/10.4028/www.scientific.net/amr.1096.477
https://doi.org/10.4028/www.scientific.net/amr.1096.477
Publikováno v:
Archiv der Pharmazie. 348:206-213
In this publication, we design and report the synthesis of calix[4]arene-based β-diketo derivatives as novel HIV-1 integrase (IN) inhibitors. The target compounds were obtained using Claisen condensation, and their structures were characterized by N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e56d62e858b5ca17728d67d8e4fbd2fe
https://doi.org/10.1002/ardp.201400390
https://doi.org/10.1002/ardp.201400390
Publikováno v:
RSC Advances. 5:37574-37580
We synthesized a D–π–A–π–A type dye and demonstrated its application in dye-sensitized solar cells (DSSCs). This D–π–A–π–A type dye, named C321, consisted of a triphenylamine as a donor, a 3,4-ethylenedioxythiophene (EDOT) as a π
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::482f29ba017da31a3a3647a3aeca5e49
https://doi.org/10.1039/c5ra05287d
https://doi.org/10.1039/c5ra05287d
Publikováno v:
Chinese Journal of Organic Chemistry. 40:2051
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c1bf7eb4d32ebbfc30abd3acffdc2a9
https://doi.org/10.6023/cjoc202003037
https://doi.org/10.6023/cjoc202003037
Publikováno v:
Advanced Materials Research. :49-52
A series of bis (2-tetrahydrobenzofuranyl) alkanes in good yield under solvent-free conditions from differently aromatic substituted aldehydes and 3-methyl-6,7-dihydrobenzofuran-4(5H)-one in the presence of H2SO4•SiO2as catalyst at 90oC. Their stru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5043a4cb08d87bbddc3ad25f35c01e4c
https://doi.org/10.4028/www.scientific.net/amr.1033-1034.49
https://doi.org/10.4028/www.scientific.net/amr.1033-1034.49
Publikováno v:
Advanced Materials Research. 997:128-131
A pair of triazole-linked bistetrahydrobenzofuran derivatives were prepared in high yields through Cu (II)-catalyzed click reaction under mild conditions. All of the intermediates and target compounds were characterized by NMR, IR, ESI-MS and element
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bae7bbe11682484ecba60fbc27df5694
https://doi.org/10.4028/www.scientific.net/amr.997.128
https://doi.org/10.4028/www.scientific.net/amr.997.128
Publikováno v:
Chinese Chemical Letters. 25:737-740
A series of novel calix[4]arene derivatives incorporating two triazolyl 1,3-diketo subunits in alternate positions at the lower rim were synthesized and screened for HIV integrase inhibition activity. The chemical structures of these compounds were c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0014f47e63441b5337cc581fc75bb94f
https://doi.org/10.1016/j.cclet.2014.03.012
https://doi.org/10.1016/j.cclet.2014.03.012
Publikováno v:
Advanced Materials Research. 918:32-35
Discovery of bioactive ingredients from plants and fungi is always the hot spots in medicinal chemistry. The trametenolic acid B was a bioactive lanostane-type triterpenoid inTrametes lactinea(Berk.) Pat. In this work, four semi-synthetic derivatives
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd3eeea77e223fb6b5756ff8c8c6d56b
https://doi.org/10.4028/www.scientific.net/amr.918.32
https://doi.org/10.4028/www.scientific.net/amr.918.32
Publikováno v:
ARKIVOC: Online Journal of Organic Chemistry. 2009, p220-232. 13p. 4 Diagrams, 2 Charts.