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Piperidine derivatives acetyl ester from

Verazine (37) has been the subject of a formal total synthesis (Scheme 1) based on the earlier reported versatile syntheses of solanidine and tomatidenol. As in the earlier work, Michael addition of the anion of the configurationally pure nitro-ester (30) to (29) gave the C-22 epimeric mixture (31), from which the individual diastereomers were isolated after acetylation. The (22S)-acetate (32) was converted via thioketal (34) and lactam (35) into the piperidine derivative (36). Base treatment of the N-chloro-derivative of (36) then gave verazine (37). [Pg.290]

Alkaloid biosynthesis needs the substrate. Substrates are derivatives of the secondary metabolism building blocks the acetyl coenzyme A (acetyl-CoA), shikimic acid, mevalonic acid and 1-deoxyxylulose 5-phosphate (Figure 21). The synthesis of alkaloids starts from the acetate, shikimate, mevalonate and deoxyxylulose pathways. The acetyl coenzyme A pathway (acetate pathway) is the source of some alkaloids and their precursors (e.g., piperidine alkaloids or anthraniUc acid as aromatized CoA ester (antraniloyl-CoA)). Shikimic acid is a product of the glycolytic and pentose phosphate pathways, a construction facilitated by parts of phosphoenolpyruvate and erythrose 4-phosphate (Figure 21). The shikimic acid pathway is the source of such alkaloids as quinazoline, quinoline and acridine. [Pg.67]

The a is L-lysine, as in the case of piperidine, but the f3 is different. The /3 is a-aminoadipic acid 6-semialdehyde. The q> is L-pipecolic acid, which is synthesized in plants from piperideine-6-carboxylic acid. In the case of many other organisms, the obligatory intermedia (q>) is derived from the /3. The

ring structure. The indolizidine nucleus will be formed only in the synthesis of the x- The deep structmal change occms when

Claisen reaction with acetyl or malonyl CoA (Cra/mCoA) and the ring closme process (by amide or imine) to 1-indolizidinone, which is the x- The second obligatory intermedia ( k ) only has the indolizidine nucleus. [Pg.97]


See other pages where Piperidine derivatives acetyl ester from is mentioned: [Pg.188]    [Pg.551]    [Pg.228]    [Pg.9]    [Pg.736]    [Pg.228]    [Pg.228]    [Pg.811]    [Pg.497]    [Pg.429]   
See also in sourсe #XX -- [ Pg.14 , Pg.557 , Pg.578 ]




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Acetyl derivative

Acetyl esters

Acetylation deriv

Ester acetylation

Ester derivation

Ester derivatives

From piperidines

Piperidine, derivatives

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