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Acetogenins stereoselective synthesis

A double intramolecular Sn> O-cyclization for the stereoselective synthesis of the bistetra-hydrofuran core of Acetogenins has been achieved <99JOC2259>. [Pg.151]

Total Stereoselective Synthesis of Acetogenins of Annonaceae A New Class of Bioactive Polyketides... [Pg.193]

It is to answer so many questions that different groups around the world are studying the total stereoselective synthesis of acetogenins of Annonaceae. [Pg.196]

Stereoselective intramolecular oxymercuration of carbohydrate derivatives was proposed as the key reaction for efficient preparation of mono- and dihydroxylated unsymmetrical bis-tetrahydrofuran skeletons present in naturally occurring biologically active acetogenins. The trans- and. mz-selective intramolecular oxymercurations were explored in an enantioselective synthesis of the bis-tetrahydrofuran skeleton of mucoxin (Fig. 57).73... [Pg.250]


See other pages where Acetogenins stereoselective synthesis is mentioned: [Pg.16]    [Pg.136]    [Pg.152]    [Pg.527]    [Pg.16]    [Pg.661]    [Pg.196]    [Pg.135]    [Pg.365]    [Pg.664]    [Pg.360]    [Pg.1609]    [Pg.218]   


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Acetogenin synthesis

Acetogenins synthesis

Stereoselective synthesis

Stereoselective synthesis of acetogenins

Stereoselectivity synthesis

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