Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Rongbi Han"'
Publikováno v:
Letters in Drug Design & Discovery. 6:548-553
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83ffbcfe540ac6bbbcedeafc08b39400
https://doi.org/10.2174/157018009789108231
https://doi.org/10.2174/157018009789108231
Publikováno v:
CNSneurological disorders drug targets. 15(10)
A series of new 8-alkylamino-5, 6-dihydro-4H-benzo[f][1,2,4]triazolo [4,3-a]azepine derivatives were synthesized and screened for their anticonvulsant activities by the maximal electroshock (MES) test, subcutaneous pentylenetetrazol (scPTZ) test, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::677a35861fe6981cb8cdc77db0ed6f3b
https://pubmed.ncbi.nlm.nih.gov/26996166
https://pubmed.ncbi.nlm.nih.gov/26996166
Autor:
Byung Min Lee, Rongbi Han, Young Moo Jun, Younbong Park, Gil Hwan Ahn, Kee In Son, Byeong Hyo Kim
Publikováno v:
Tetrahedron Letters. 47:7295-7299
2-Nitroaryl aldehydes, ketones, and imines were reductively cyclized to 2,1-benzisoxazoles with good yields in the presence of indium and iodine in MeOH. Under a similar condition, N-(2-nitrobenzylidene)anilines were produced mixtures of 2,1-benzisox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4050da4523f28c76faef8219a7c17863
https://doi.org/10.1016/j.tetlet.2006.08.027
https://doi.org/10.1016/j.tetlet.2006.08.027
Autor:
Byung Mook Kim, Byeong Hyo Kim, Byung Min Lee, Rongbi Han, Young Moo Jun, Bong Kwan Soh, Insik Jeon, Tae Hee Han
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 179:167-175
Photostimulated tethered free radical reactions for the intramolecular cyclizations towards α-tetralones, N-containing α-tetralone analogues, 3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]chromen-5-ones and 2,3,4,4a,6,10b-hexahydropyrano[3,2-c]quinolin-5-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75418fd3ab550aeceecf557b53eacfdb
https://doi.org/10.1016/j.jphotochem.2005.08.009
https://doi.org/10.1016/j.jphotochem.2005.08.009
Publikováno v:
Synthetic Communications. 31:3577-3586
By applying indium, Ac2O, MeOH, and catalytic amount of InCl3 in CHCl3 solution, nitroarenes were transformed into N,O-diacylated N-arylhydroxylamines in moderate to excellent yields. *Dedicated to Professor Jack W. Timberlake on the occasion of his
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f850ba97251232e7e0006bf0a8bed07
https://doi.org/10.1081/scc-100107004
https://doi.org/10.1081/scc-100107004
Publikováno v:
Tetrahedron Letters. 41:2137-2140
2-Nitro-substituted acylbenzenes or iminobenzenes such as 2-nitrobenzaldehydes, 2′-nitroacetophenone, and N-(2-nitrobenzylidene)anilines were cyclized toward 2,1-benzisoxazoles in the presence of 2-bromo-2-nitropropane and indium in an MeOH/H2O sol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e135b241532e11b5e09df7c143537e5f
https://doi.org/10.1016/s0040-4039(00)00098-8
https://doi.org/10.1016/s0040-4039(00)00098-8
Publikováno v:
Tetrahedron Letters. 44:77-79
N-Arylacetamides were prepared in excellent yields from nitroarenes in the presence of acetic anhydride, acetic acid and indium by a one-pot procedure.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6820413f1b52f65d239ebb7bb098acb
https://doi.org/10.1016/s0040-4039(02)02479-6
https://doi.org/10.1016/s0040-4039(02)02479-6
Publikováno v:
ChemInform. 31
2-Nitro-substituted acylbenzenes or iminobenzenes such as 2-nitrobenzaldehydes, 2′-nitroacetophenone, and N-(2-nitrobenzylidene)anilines were cyclized toward 2,1-benzisoxazoles in the presence of 2-bromo-2-nitropropane and indium in an MeOH/H2O sol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6487472aa26015c0b674306e1e121c9
https://doi.org/10.1002/chin.200025136
https://doi.org/10.1002/chin.200025136
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf7b6c04c661d16b7c5bb6f255da2429
https://doi.org/10.1002/chin.200030113
https://doi.org/10.1002/chin.200030113
Publikováno v:
ChemInform. 32
In a mild reaction with SmI2, aldimines have been converted into homoallyl amines in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13becdf5cf059ff4d426e9a82df2f72a
https://doi.org/10.1002/chin.200149046
https://doi.org/10.1002/chin.200149046