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Limonium

Hydroxybenzoylrhamnoside) Limonium sinense aerial parts Plumbaginaceae 434... [Pg.774]

Limonium perezii 1 L. gmelinii / Murraya paniculata Oricia suaveolens... [Pg.75]

A new alkaloid, 4-formyl-8-hydroxyquinoline, was isolated from Broussonetia zeylanica the structure was apparent from spectral studies and by its Wolff-Kishner reduction to 8-hydroxy-4-methylquinoline. 6-Hydroxykynurenic acid was obtained from Limonium species " this is the first time that the compound has been isolated from members of the Plumbaginaceae. A new synthesis of echinopsine has been carried out (Scheme 2). ... [Pg.76]

The optimal concentration of irradiated chitosan for the growth of shoot clusters and shoot multiplication rate was 70 mg/L for Chrysanthemum, 50-100 mg/L for Lisianthus, and 30-100 mg/L for Limonium. Fresh biomass increased by 68.1% for Chrysanthemum, 48.5% for Lisianthus, and 53.6% for Limomum (Luan et al. 2005). A comparison of the above results showed that the molecular wdght of irradiated chitosan is smaller, and the bioactivity of plant-growth promotion is stronger. [Pg.620]

Occupational asthma and contact urticaria from dried flowers of Limonium tartaricum. Allergy 48 285-290 176. [Pg.214]

A hobby gardener developed delayed urticaria from elm, Ulmus spp., with inhibition by aluminum sulphate [399]- Other plants causing contact urticaria in this group include Lily longifolium and tulip [400], Limonium tartaricum (from dried flowers) [401], and chrysanthemum [402]. For a more complete listing of contact urticaria to plants see Lahti [403] and Table 6. [Pg.755]

Pigment from Oxalis cernua, also present in Chirita micromusa, Limonium bonduellii and Petrocosmea kerrii. Yellow cryst. (EtOH aq.). Mp 250-258°. [(xf -13° (Py). 6-0-13-D-Glucopyranoside [633-15-8]. Aureusin... [Pg.28]

Coumaranones such as (31) have been suggested as intermediates in the synthesis of the yellow aurone pigments and it is apposite that a related structure (32) has recently been found in the heartwood of Acacia crombei. ° This represents the first report of a spirocoumaranone in nature. At one time, all known plant aurones had a catechol B-ring [e.g. (33)] and their synthesis seemed to be in some way related to this fact. However, an exception to this regularity has now appeared. Asen and Plimmer have discovered an aurone with a single hydroxy-group in its B-ring, namely (34), in yellow flowers of a Limonium cultivar, where it occurs in conjunction with (33) and the chalcone (26). [Pg.230]

Solanaceae) (leaves) (145) Thapsia villosa L. (Apiaceae) (fruits) (146) Limonium perezii E.T. Hubb. L. gmelinii (Willd.) Kuntze (Plumbaginaceae) (147) Ephedra spp. (Ephedraceae) (148)... [Pg.158]


See other pages where Limonium is mentioned: [Pg.805]    [Pg.713]    [Pg.171]    [Pg.86]    [Pg.85]    [Pg.129]    [Pg.992]    [Pg.994]    [Pg.1011]    [Pg.713]    [Pg.431]    [Pg.123]    [Pg.123]    [Pg.190]    [Pg.307]    [Pg.615]    [Pg.617]    [Pg.382]    [Pg.8]    [Pg.628]    [Pg.629]    [Pg.205]    [Pg.748]    [Pg.174]   
See also in sourсe #XX -- [ Pg.571 ]




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Limonium perezii

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