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Molecular chromonics

A mass spectral study of 2-methyl-, 3-methyl- and 2,3-dimethyl-chromone (136), (137) and (138) has been reported (790MS345). In each case the molecular ion appears as the base peak, together with ions which correspond to [M-CO]-, [M-CHO]t, [RDA]t, [RDA + H]+ and [RDA-CO]t. Metastable peaks confirmed that the formation of [M-CHO]- occurs in two steps from [M]t. The reaction pathway for (136) and (138) is given in equation (2). In compound (137), [M-CHO]t is an abundant fragment ion (60%, cf. 35% for 136). That its generation occurs by more than one route is suggested not only by its high abundance, but also by the appearance of appropriate metastable ion peaks two pathways are operative (Scheme 17). [Pg.613]

Chalcone synthase (CHS), the first plant natural product polyketide synthase (PKS) to be characterized at the molecular level (39), catalyzes the condensation of 4-coumaroyl-CoA with three molecules of malonyl-CoA to afford naringenin chalcone, a precursor of the major classes of plant flavonoids. The cloning of a novel type III pentaketide chromone synthase (PCS) from aloe (Aloe arborescens, Liliaceae) rich in aromatic polyketides, especially quinones such as aloe-emodin and emodin, resulted in... [Pg.489]

The phosphorohydrazide derivatives of chromone seem to be very interesting due to their potential biological activity and the possible application in cancer chemotherapy. Figures 4 and 5 present the molecular structures of two such compounds ( )-3- [(diphenoxyphosphoryl)-2-methylhydrazone]-methyleno -... [Pg.495]

Among vast varieties of lyotropic LCs, chromonic mesophases are the families of new research target starting only about two or three decades ago. The properties are different from those of ordinary lyotropic mesogens of surfactant type. The molecules constitute aromatic(s) in the center, and hydrophilic parts are scattered around the molecules rather than aliphatic structures. Therefore, they are rigid and planar disklike or planklike, rather than micelles of flexible molecular assemblies of ordinary surfactants. The molecules aggregate in solution to form... [Pg.277]

Molecular iodine in the synthesis of chromone-type compounds 12COS 583. [Pg.292]


See other pages where Molecular chromonics is mentioned: [Pg.586]    [Pg.216]    [Pg.178]    [Pg.526]    [Pg.100]    [Pg.40]    [Pg.604]    [Pg.613]    [Pg.614]    [Pg.615]    [Pg.716]    [Pg.586]    [Pg.660]    [Pg.216]    [Pg.72]    [Pg.604]    [Pg.613]    [Pg.614]    [Pg.615]    [Pg.716]    [Pg.216]    [Pg.586]    [Pg.27]    [Pg.343]    [Pg.660]    [Pg.182]    [Pg.216]    [Pg.196]    [Pg.139]    [Pg.140]    [Pg.586]    [Pg.285]    [Pg.280]    [Pg.27]    [Pg.2151]    [Pg.467]    [Pg.333]    [Pg.237]    [Pg.404]    [Pg.216]   
See also in sourсe #XX -- [ Pg.2 ]

See also in sourсe #XX -- [ Pg.2 , Pg.983 ]




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Chromone

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