Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ya-bing Wei"'
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 1, Pp o205-o205 (2009)
Molecules of the title compound, C10H12FNO3, are nearly planar considering all non-H atoms with a mean deviation of 0.0288 Å. Molecules are linked through intermolecular N—H...O and N—H...F hydrogen bonds.
Externí odkaz:
https://doaj.org/article/c21661816fb9419db75a97755be60054
Publikováno v:
Tetrahedron. 68:9186-9191
Utilizing toluene/isopropanol (20:1 to 40:1) as a solvent and KHF2 as an additive, the rhodium/diene-catalyzed asymmetric arylation (RCAA) reaction of arylboronic acids to N-Boc-protected α,β-unsaturated δ-lactam proceeded smoothly to afford chira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0ff6477f54d690a7f635c38cab6c96a
https://doi.org/10.1016/j.tet.2012.09.001
https://doi.org/10.1016/j.tet.2012.09.001
Publikováno v:
Chinese Chemical Letters. 21:1338-1341
A versatile synthesis of novel zanamivir analogues modified at C-4 and C-8 positions was described. The formation of amides from the acid with corresponding amines, followed by click chemistry generated the triazole substituted compounds as novel ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84e8917caddf1d1f564159e34ab29b1c
https://doi.org/10.1016/j.cclet.2010.06.021
https://doi.org/10.1016/j.cclet.2010.06.021
Autor:
Jingshan Shen, Guangxin Xia, Wei-Xi Jin, Ruyun Ji, Ya-Bing Wei, Tian Guanghui, Xinjian Chen, Shunan Lai
Publikováno v:
Chinese Journal of Chemistry. 25:241-245
Novel pyridopyrazolopyrimidinone derivatives were designed and synthesized as potential PDE5 inhibitors. The target compounds demonstrated significant inhibitory activity against human platelet PDE5, but less potent than sildenafil.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0906c205cb7f95070e75a571113ebf71
https://doi.org/10.1002/cjoc.200790048
https://doi.org/10.1002/cjoc.200790048
Publikováno v:
ChemInform. 44
Utilizing toluene/isopropanol (20:1 to 40:1) as a solvent and KHF2 as an additive, the rhodium/diene-catalyzed asymmetric arylation (RCAA) reaction of arylboronic acids to N-Boc-protected α,β-unsaturated δ-lactam proceeded smoothly to afford chira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3180895c425713c9612ebbdcacdc6c10
https://doi.org/10.1002/chin.201311149
https://doi.org/10.1002/chin.201311149