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Guibourtia

Fuendjiep, V. et al., Chalconoid and stilbenoid glycosides from Guibourtia tessmanii. Phytochemistry, 60, 803, 2002. [Pg.125]

Ej-3,4 -di methoxy-5-ruti nosy 1 stilbene Guibourtia tessmannii 16... [Pg.459]

Nyemba AM, Mpondo TN, Kimbu SF, Connolly JD (1995) Stilbene glycosides from Guibourtia tessmannii. Phytochemistry 39 895-898... [Pg.1943]

Fuendjiep V, Wji J, Tillequin F, Mulholl DA, Budzikiewicz H, Fomnm ZT, Nyemba AM, Koch M (2002) Chalconoid and stilbenoid glycosides frmn Guibourtia tessmanii. Phytochemistry 60 803-806... [Pg.1943]

The proguibourtinidins obtained from Guibourtia coleosperma that carry a 3,4,3, 5-tetrahydroxystilbene terminating unit are among the most interesting proanthocyanidins that have been isolated recently. As in most other ly i-cis proanthocyanidins the compound 50 contains only [4-yff] or A-trans substitution. The 2, i-trans dimer has a [4-a] bond and, interestingly, the trimer 51 has both a 2,3-cis and a 2,3-trans proanthocyanidin unit (345). Another trimer with mixed 2,3-stereochemistry in the proguibourtinidin units was isolated, but its structure was not defined. [Pg.613]

Roux D G 1959 Flavan-3,4-diols and leuco-anthocyanidins of Guibourtia spp. Nature 183 890-891... [Pg.648]

Roux D G, DeBruyn G C 1963 Condensed tannins. 17. Isolation of 4, 7-dihydroxyflavan-3,4-diol from Guibourtia colesperma. Biochem J 87 439... [Pg.648]

See other pages where Guibourtia is mentioned: [Pg.578]    [Pg.123]    [Pg.220]    [Pg.90]    [Pg.459]    [Pg.459]    [Pg.803]    [Pg.804]    [Pg.806]    [Pg.459]    [Pg.50]    [Pg.407]    [Pg.173]    [Pg.355]    [Pg.1904]    [Pg.606]    [Pg.1255]    [Pg.1255]    [Pg.127]    [Pg.230]   
See also in sourсe #XX -- [ Pg.671 ]



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Guibourtia tessmanii

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