Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Dexuan Xiang"'
Publikováno v:
Applied Physics Letters. 122
It is widely recognized that hybrid (organic/inorganic) light emitting diodes (LEDs) are of concern because they use an organic material instead of rare earth phosphors, but extending their lifetime remains challenging. To construct organic luminesce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a79ac0ce821e32b0f034dc7f0162f348
https://doi.org/10.1063/5.0146021
https://doi.org/10.1063/5.0146021
Publikováno v:
Optical Materials. 126:112226
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4476355cfa4b0f13266c469173b12d4f
https://doi.org/10.1016/j.optmat.2022.112226
https://doi.org/10.1016/j.optmat.2022.112226
Autor:
Hongwei Lin, Huan Yao, Xiyue Gao, Li Zhang, Qionglin Luo, Yuejun Ouyang, Bailin Xiang, Shasha Liu, Dexuan Xiang
Publikováno v:
Chemistry Letters; Nov2021, Vol. 50 Issue 11, p1879-1882, 4p
Publikováno v:
RSC Adv.. 3:1346-1349
A facile and efficient one-pot synthesis of substituted 2,5-dihydrofurans from cinnamaldehydes and β-oxo amides is described, and a mechanism involving the intramolecular oxidative cyclization of penta-2,4- dienamides, i.e. Knoevenagel condensation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbebc60248726c5ae99bc85937810dd8
https://doi.org/10.1039/c2ra21820h
https://doi.org/10.1039/c2ra21820h
Publikováno v:
RSC Adv.. 3:386-389
An unprecedented solvent-controlled, regio-switchable Knorr-type reaction for the synthesis of pyrazoles has been realized in the cyclocondensation of β-aminoenones with hydrazides. Single regioisomer of 3- or 5-arylaminopyrazole can be obtained sim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7b3f5d57b88fd0373f4f0fe43f7a1c8
https://doi.org/10.1039/c2ra22647b
https://doi.org/10.1039/c2ra22647b
Publikováno v:
Synthesis. 44:705-710
Efficient and divergent one-pot synthesis of cyclopropyl amides and esters from readily available 1-acetylcyclopropanes via iodoform reaction based on the selection of reaction conditions is reported. A series of substituted cyclopropyl amides were s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbbe96baa95773c8ef5cf499f85cded9
https://doi.org/10.1055/s-0031-1289693
https://doi.org/10.1055/s-0031-1289693
Publikováno v:
Organic Letters. 14:644-647
A highly regioselective synthesis of 3-arylamino- and 5-arylaminoisoxazoles from enaminones based on reaction condition selection is reported. 3-Arylaminoisoxazoles were produced by treating enaminones with aqueous hydroxylamine in DMF at 100 °C, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fac053d3f1a43305664e7fc1fc517fbb
https://doi.org/10.1021/ol203282h
https://doi.org/10.1021/ol203282h
Publikováno v:
Synlett. 2011:2187-2190
A facile and efficient one-pot synthesis of pyrano[2,3-b]quinolines has been developed via the Combes-type reaction of readily available enaminones, 2-arylamino-3-acetyl-5,6-dihydro-4H-pyrans, mediated by trifluoromethanesulfonic acid under solvent-f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5218d8df231b1337e953fac4a60a673e
https://doi.org/10.1055/s-0030-1261198
https://doi.org/10.1055/s-0030-1261198
Publikováno v:
Synthesis. 2009:1797-1800
A facile and practical one-pot synthesis of beta-oxo thioamides from beta-oxo amides has been developed. By treatment with isothiocyanates in ethanol in the presence of potassium carbonate, a series of beta-oxo amides was converted, under reflux, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c714af0e3696d24ae73e78228ba8463c
https://doi.org/10.1055/s-0028-1088078
https://doi.org/10.1055/s-0028-1088078
Publikováno v:
Tetrahedron. 64:4959-4966
A facile and efficient synthesis of substituted alpha-alkylidene-beta-lactams have been developed via a NaOH-promoted intramolecular aza-Michael addition of alpha-carbamoyl, alpha-(1-chlorovinyl) ketene-S,S-acetals and subsequent nucleophilic vinylic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc5ba28cd60889383b1fedd61c0c5150
https://doi.org/10.1016/j.tet.2008.03.093
https://doi.org/10.1016/j.tet.2008.03.093