Asymmetric Aldol Reactions di Aswini Kumar Giri, Saumen Hajra edito da SPS
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Asymmetric Aldol Reactions

Synthesis of Paraconic Acids & Lignans

Editore:

SPS

EAN:

9783639713312

ISBN:

3639713311

Pagine:
244
Formato:
Paperback
Lingua:
Tedesco
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Descrizione Asymmetric Aldol Reactions

Chiral auxiliary based and organocatalyzed aldol reactions have been used for the asymmetric synthesis of various natural products. These reactions steps have been used in synthesizing ¿-butyrolactone containing natural products and their analogs. An asymmetric route for one-pot synthesis of trans- and cis-4,5-disubstituted-¿-butyrolactones via reagent sequence controlled syn- and anti- aldol reactions of N-succinyl-2-oxazolidinone are described. Mechanistic studies are discussed. Using these asymmetric syn- and anti-aldol reactions of chiral N-succinyl-2-oxazolidinones, trans-paraconic acids and cis-paraconic acids are synthesized in both of their enantiomeric forms. Enantioselective one-pot synthesis of ¿-(hydroxyalkyl)-¿-butyrolactones employing cross-aldol reaction catalyzed by an organocatalyst is described. Efficient routes for the asymmetric synthesis of (¿)-enterolactone, natural hydroxyenterolactone and its analog utilizing organocatalytic asymmetric cross-aldol reaction and C-alkylation as the key steps are achieved. Similar routes have provided chiral intermediates, which could be converted to epi-isohydroxymatairesinol and (7¿R)-7¿-hydroxymatairesinol.

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