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Calystegins

Scheme 5 Carbohydrate carbocyclization in the total synthesis of calystegine B2 (28) [27,28]... Scheme 5 Carbohydrate carbocyclization in the total synthesis of calystegine B2 (28) [27,28]...
The Staudinger/aza-Withg procedure has recently also been used by Mellet and Fernandez for the synthesis of calystegine B2, B3, and B4 analogues, emphasizing the growing importance of this methodology [12]. [Pg.498]

The Hanna group developed a rapid route to (+)-calystegine B2 (7-79) [35], a natural product with strong glycosidase enzyme-inhibiting properties [36]. As the key step, a triple domino procedure first published by Madsen and coworkers was em-... [Pg.508]

Scheme 7.21. Zinc-mediated domino reaction in the total synthesis of (+)-calystegine B2 (7-79). Scheme 7.21. Zinc-mediated domino reaction in the total synthesis of (+)-calystegine B2 (7-79).
Preparation of polyhydroxylated 6-oxanortropane glycomimetics (e.g. 32), structurally related to the glycosidase inhibitor family of the calystegines, was reported. The synthetic strategy involves the furanose/piperidine... [Pg.234]

A syndrome in livestock occurs with respect to Ipomoea species, which have been found to poison sheep in Australia and goats in Africa (Molyneux et ah, 1995). The analysis of 7. calobra and 7. polpha from Queensland showed that these plants contain not only calystegines B2 and Cl, but also swainsonine. An... [Pg.45]

Examples of other fluorinated inhibitors, mainly of D-glucosidases, are the 2-deoxy-2-fluoro derivative 106 (Scheme 27) of miglitol (A-hydroxyethy I -1 -deoxynoj i i i my-cin, 107),229 4-deoxy-4,4-difluoroisofagomine (108),230 3-deoxy-3-fluoro-calystegin B2 (109),231 the 1-deoxyfluoro derivative (110) of 2,5-dideoxy-2,5-imino-D-mann-itol,232 as well as the 3-deoxyfluoro analogue (111) of nonnatural l-DMDP (2,5-dideoxy-2,5-imino-L-mannitol)233 and the 3-deoxy-3,3-difluoro derivative (112) of 2,5-dideoxy-2,5-imino-D-glucitol (113).234 All of these are weaker inhibitors than the parent compounds. l,4,6-Trideoxy-6-fluoro-l,4-imino-D-mannitol (114) was prepared by Winchester and coworkers.210... [Pg.220]

Many alkaloids can be produced by root cultures. The most known applications are with anabasine, nicotine, harmine, harmaline, hyoscyamine, calystegine, scopolamine, Enzymes such as... [Pg.204]

Analysis and Biological Activities of Potato Clycoalkaloids, Calystegine Alkaloids, Phenolic Compounds, and Anthocyanins... [Pg.127]

This limited overview on the analysis of four classes of the following secondary potato metabolites is, except for anthocyanins, largely limited to our own studies of glycoalkaloids, calystegine alkaloids, and phenolic compounds. Because interest in these potato constituents arises from potential health benefits and occasional toxicity, we also include in this overview a brief discussion of these aspects that relate to composition and a description of experimental methods. The interested reader should consult the cited references for an entry into the extensive worldwide literature on the diverse analytical and biological aspects for these metabolites. [Pg.127]

Table 6.2 Glycoalkaloid and calystegine content of potato flesh, potato peel, and whole potatoes of eight potato cultivars... [Pg.135]

We validated and improved a GC-MS method to measure the two major potato calystegines A3 and B2 in freeze-dried potato peel and potato flesh samples (Friedman et al., 2003c). We used this method to analyze the same potatoes that we previously analyzed for glycoalkaloids (Table 6.2). [Pg.137]

Figure 6.4 illustrates the separation on GC-MS total ion chromatograms of calystegines A3 and B2 extracted from potato powders. Results of the GC-MS analyses for calystegines A3 and B2 are shown in Table 6.2. For whole potatoes, there is a 12-fold variation from lowest... [Pg.138]


See other pages where Calystegins is mentioned: [Pg.278]    [Pg.279]    [Pg.317]    [Pg.527]    [Pg.527]    [Pg.45]    [Pg.49]    [Pg.49]    [Pg.69]    [Pg.69]    [Pg.413]    [Pg.192]    [Pg.221]    [Pg.223]    [Pg.232]    [Pg.232]    [Pg.266]    [Pg.278]    [Pg.287]    [Pg.290]    [Pg.292]    [Pg.215]    [Pg.135]    [Pg.135]    [Pg.136]    [Pg.136]    [Pg.136]    [Pg.136]    [Pg.136]    [Pg.137]    [Pg.138]    [Pg.138]    [Pg.138]    [Pg.138]   
See also in sourсe #XX -- [ Pg.495 ]

See also in sourсe #XX -- [ Pg.228 ]

See also in sourсe #XX -- [ Pg.210 ]




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Alkaloids calystegines

Biosynthesis of calystegines

Boyer and Lallemand homochiral -calystegines

Calystegia sepium (Calystegines

Calystegine

Calystegine

Calystegine alkaloids

Calystegine alkaloids fractions

Calystegine alkaloids hydrophilic alkaloid

Calystegines

Calystegines Convolvulaceae family

Calystegines biosynthesis

Calystegines calystegine

Calystegines detection

Calystegines isolation procedures

Calystegines nortropane alkaloids

Calystegines plant activity

Calystegines properties

Calystegines structures

Calystegines tropane alkaloids

Calystegines, glycosidase

Convolvulaceae calystegines

Convolvulaceae calystegines found

Homochiral -calystegines

Homochiral -calystegines synthesis

Solanaceae plants calystegines found

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