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Biflavonoid Structures

In combination, the class of biflavonoids represents a library of over 20,000 different molecules, each of which is capable of multiple H-bondings and hydrophobic interactions. Not all these have been found to exist in nature so far. However, biflavonoid theoretical library covers a wide range of the configurational and conformational space, thus suggesting that the scope of interesting biological activities may be extraordinary. [2] [Pg.5]

The structure of a given biflavonoid is typically elucidated using intensive ID and 2D NMR (COSY, NOESY).[10, 11] Circular dichroism (CD) is used to determine the absolute configuration in molecules that possess stereocenters. [12] Occasionally, additional spectroscopic techniques are used (MS, IR, UV and single crystal X-ray). [Pg.5]

In the present chapter, the structures of the biflavonoids are represented and included in diverse figures to illustrate their variability, rearrangements, and different stereochemistry. A number was assigned to each structure for further references. Due to the large number of molecules, the structures were classified and divided into series, each series shares a similar backbone, containing a variety of different substituents. [Pg.6]

II-7-Di-0-methyl-I-2,3,II-2,3-tetrahydro-amentoflavone Semeoarpetin Nallaflavone 11-3, 4 substituent -O-CH2-O- (methylenedioxyl). [Pg.11]

Robustaflavone series consists of two flavonoid units linked by a (I-3, II-6) bond. This series was also subdivided into the following sets structures containing two flavone imits, (l-3, II-6)-biflavones (64-73) a flavone and a flavonol imit, (I-3, II-6)-flavone-flavonol (74) a flavanone and a flavone unit, (l-3, II-6)-flavanone-flavone (75-79) a flavone and a flavanone imit, (I-3, II-6)-flavone-flavanone (80-82) and finally, a set containing structures with two flavanone units or two flavanonol units, (l-3, II-6)-biflavanones and (1-3, 11-6)-biflavanonols (83-85). [Pg.12]


This reaction was used in the synthesis of biflavonoid structures (85), which are analogues of natural compounds isolated from Garcinia species, members of the Guttiferae famOy.1 2,169... [Pg.229]


See other pages where Biflavonoid Structures is mentioned: [Pg.394]    [Pg.5]    [Pg.5]    [Pg.9]    [Pg.11]    [Pg.13]    [Pg.15]    [Pg.17]    [Pg.19]    [Pg.21]    [Pg.23]    [Pg.25]    [Pg.27]    [Pg.29]    [Pg.31]    [Pg.33]    [Pg.35]    [Pg.37]    [Pg.39]    [Pg.41]    [Pg.43]    [Pg.45]    [Pg.47]    [Pg.49]    [Pg.51]    [Pg.53]    [Pg.55]    [Pg.57]    [Pg.59]    [Pg.61]    [Pg.63]    [Pg.65]    [Pg.67]    [Pg.69]    [Pg.71]    [Pg.73]    [Pg.75]    [Pg.77]    [Pg.79]    [Pg.81]    [Pg.83]    [Pg.85]    [Pg.87]    [Pg.89]    [Pg.91]    [Pg.93]    [Pg.95]    [Pg.189]    [Pg.307]   


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Biflavonoids

Structural Variations of Biflavonoids

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