A novel enantiospecific synthesis of (S)-(–)-methyl 6,8-dihydroxyoctanoate, a precursor of (R)-(+)-α-lipoic acid
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1990/C3/C39900000729
Reference12 articles.
1. Proof that the absolute configuration of natural α-lipoic acid is R by the synthesis of its enantiomer [(S)-(–)-α-lipoic acid] from (S)-malic acid
2. Enantiospecific synthesis of (R-(+)-α-lipoic acid from d-glucose
3. Stereospecific synthesis of α-lipoic acid
4. Asymmetric synthesis via acetal templates. 12. Highly diastereoselective coupling reactions with a ketene acetal. An efficient, asymmetric synthesis of R-(+)-α-lipoic acid
5. Enantioselective synthesis of R-(+)-α-lipoic acid
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