Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Hong-Ru Dong"'
Autor:
Hong-Ru Dong1 1000467@luas.edu.cn
Publikováno v:
Indian Journal of Chemistry (0019-5103). 2023, Vol. 62 Issue 1, p53-59. 7p.
Publikováno v:
Indian Journal of Chemistry. Sect B. Dec2021, Vol. 60B Issue 12, p1629-1635. 7p.
Autor:
Hong-Ru Dong, Jian-Guo Wu
Publikováno v:
Heterocyclic Communications. 24:109-112
New 1-aryl-4-[(aziridine-1-yl)diarylmethyl]-5-methyl-1H-1,2,3-triazole derivatives 7a–i were synthesized by a one-pot reaction of diaryl-(1-aryl-5-methyl-1H-1,2,3-triazol-4-yl)methanols 6a–i derived from 1-aryl-5-methyl-1H-1,2,3-triazole-4-carbox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2126ff59c33a9063209b8f2b6d9b2f3
https://doi.org/10.1515/hc-2017-0144
https://doi.org/10.1515/hc-2017-0144
Publikováno v:
RSC Advances. 5:10768-10772
One-pot, atom-economical, catalyst-free and tri-component domino reactions are applied to the diversity-oriented synthesis (DOS) of disubstituted piperazine derivatives under mild conditions with moderate to high yields. This protocol exhibits potent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b218db28a62f47cb23c2a688898db823
https://doi.org/10.1039/c4ra14811h
https://doi.org/10.1039/c4ra14811h
Some new 1-aryl-4-[(aziridine-1-yl)diaryl-methyl]-5-methyl-1H-1,2,3-triazole derivatives 7j–s were synthesized by the one-pot reaction of diaryl-(1-aryl-5-methyl-1H-1,2,3-triazol-4-yl)methanol compounds 6j–s formed from 1-aryl-5-methyl-1H-1,2,3-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d3219b66c27f4561b483a8d2a56eaef
Publikováno v:
Tetrahedron. 70:8405-8412
An efficient iodine-mediated cascade synthesis of 3-aza-bicyclo[3.1.0]hex-2-ene derivatives from easily prepared N -allyl enamines has been developed. The advantages of the reaction include facilitative preparation of substrates 3a – t , good funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::745a919ff6ee522ed7c89c599c3f445f
https://doi.org/10.1016/j.tet.2014.08.043
https://doi.org/10.1016/j.tet.2014.08.043
Publikováno v:
Green Chem.. 16:3454-3457
Domino nucleophilic addition was used for four-component Al2O3-catalyzed environmentally friendly synthesis of polysubstituted β-cyanopropan-1-one. Domino nucleophilic addition involves removal of the cyano group linked to active methylene by the ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::968d3aede5913e30980ed6021dfa5fed
https://doi.org/10.1039/c4gc00386a
https://doi.org/10.1039/c4gc00386a
Publikováno v:
RSC Adv.. 4:55827-55831
A novel and efficient one-pot method has been developed for the synthesis of 2-substituted-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one derivative by the combination of [3 + 3] cycloaddition, reduction, deamination reactions. The fused heterocyclic com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ef1ced606bff4ba3aab5843af0196af
https://doi.org/10.1039/c4ra02714k
https://doi.org/10.1039/c4ra02714k
Publikováno v:
Journal of Chemical Crystallography. 40:1078-1081
(5-Methyl-3-phenyl-1H-pyrazol-1-yl)-[5-(p-tolylamino)-2H-1,2,3-triazol-4-yl]methanone was synthesized and characterized by 1H NMR, MS and IR spectra data. The structure of title compound was identified by X-ray diffraction. Compound, C20H18N6O, Mr =
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a8b3d84feca85242696abdb433f392e
https://doi.org/10.1007/s10870-010-9798-3
https://doi.org/10.1007/s10870-010-9798-3
Publikováno v:
Journal of Chemical Crystallography. 39:87-90
5-Methyl-1-(1-naphthyl)-1,2,3-triazol-4-carboxyl acid 3 was synthesized from 1-aminonaphthalene. The yielded product 3 was investigated with X-ray crystallographic, NMR, MS and IR techniques. Compound 3, C14H11N3O2, Mr = 253.26, crystallizes in the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7e82ceecd5458f128f8f5f7fea560a2
https://doi.org/10.1007/s10870-008-9408-9
https://doi.org/10.1007/s10870-008-9408-9