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Hyacinthacines family

Other synthetic approaches to hyacinthacine skeleton using the xylose-derived nitrone were reported. In 2010, the synthesis of (—)-hyacinthacine A3 66 (the enantiomer of the naturally occurring (+)-hyacinthacine A3) was described by Hu et al. [20]. This member of the hyacinthacines family includes a chiral center at the C-5 position of the B-ring (Scheme 12). [Pg.387]


See other pages where Hyacinthacines family is mentioned: [Pg.373]    [Pg.375]    [Pg.377]    [Pg.379]    [Pg.381]    [Pg.383]    [Pg.385]    [Pg.387]    [Pg.389]    [Pg.391]    [Pg.393]    [Pg.395]    [Pg.397]    [Pg.399]    [Pg.401]    [Pg.403]    [Pg.405]    [Pg.407]    [Pg.409]    [Pg.411]    [Pg.413]    [Pg.414]    [Pg.417]    [Pg.419]   


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Hyacinthacine

Hyacinthacines

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