Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ye-Fei Nan"'
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 5, Pp o1105-o1105 (2010)
The title compound, C12H16O5, is a derivative of β-(3,4-dihydroxyphenyl)-α-hydroxy acid. The crystal packing is stabilized by intermolecular O—H...O hydrogen bonds.
Externí odkaz:
https://doaj.org/article/2ef4b940c6364ff792c10c69b286499c
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 3, Pp o566-o566 (2008)
In the title compound, C12H13NO5, the azlactone of vanillin, the acrylic acid side chain has a trans extended conformation. There are intermolecular N—H...O and O—H...O hydrogen bonds in the crystal structure.
Externí odkaz:
https://doaj.org/article/6414bfbc433c40dbbcb926211041641e
Publikováno v:
In Thermochimica Acta 2003 406(1):77-87
Publikováno v:
Current Pharmaceutical Analysis. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::901357976fbcafcf20d9404a30a059f6
https://doi.org/10.2174/1573412913666161110111715
https://doi.org/10.2174/1573412913666161110111715
Publikováno v:
Tetrahedron: Asymmetry. 22:4-7
The highly enantioselective synthesis of ( R )-isopropyl 3-(3′,4′-dihydroxyphenyl)-2-hydroxypropanoate and its enantiomer has been achieved starting from 3,4-dihydroxybenzaldehyde. The stereogenic centers were established through asymmetric dihyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20dbbe0fc14a8e8065ee613c80a52a12
https://doi.org/10.1016/j.tetasy.2010.11.030
https://doi.org/10.1016/j.tetasy.2010.11.030
Publikováno v:
Chromatographia. 71:1031-1037
A simple, sensitive and rapid method for the analysis of jasminoidin in rabbit plasma by liquid chromatography coupled to tandem mass spectrometry was developed. Detection was by positive ion electrospray ionization in multiple reactions monitoring m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::264eba12fad85d20725e98df78909715
https://doi.org/10.1365/s10337-010-1572-3
https://doi.org/10.1365/s10337-010-1572-3
Publikováno v:
Asian Journal of Chemistry. 25:7158-7160
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35be90e78897a069266f0f1e8b6f3216
https://doi.org/10.14233/ajchem.2013.14496
https://doi.org/10.14233/ajchem.2013.14496
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 62:o3742-o3743
In the title compound, C10H10Br2O2, the angle between the dibromovinyl group and the benzene ring is 42.2 (2)°.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d82b33653422f0b67ee1f1a06da8836a
https://doi.org/10.1107/s1600536806026262
https://doi.org/10.1107/s1600536806026262
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 62:o3233-o3234
In the title compound, C13H16O4, the two ester groups adopt syn- and anti-conformations. The two carbonyl O atoms are acceptors of acetylene H atoms in C—H⋯O interactions which, together with van der Waals contacts, determine the crystal pack
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3939f39f9f49e85202d29dddf01a2a4
https://doi.org/10.1107/s1600536806025505
https://doi.org/10.1107/s1600536806025505
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 62:o2385-o2386
In the crystal structure of the title compound, C18H16O5, O—H⋯O hydrogen bonds connect the molecules into centrosymmetric dimers that form stacks down the a axis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1df6a5ed8b58b6b8a3fd43a937de486f
https://doi.org/10.1107/s160053680601734x
https://doi.org/10.1107/s160053680601734x