Natural Occurrence of Enantiomeric and meso‐Astaxanthin 1. Ex Lobster Eggs (Homarus gammarus)
- 23 April 1980
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 63 (3) , 711-715
- https://doi.org/10.1002/hlca.19800630321
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Absolute Configuration of ActinioerythrinHelvetica Chimica Acta, 1978
- Synthese von optisch aktiven, natürlichen Carotinoiden und strukturell verwandten Naturprodukten. II. Synthese von (3 S, 3′S)‐AstaxanthinHelvetica Chimica Acta, 1978
- 1H‐NMR.‐, 13C‐NMR.‐, UV.‐ und CD.‐Daten von synthetischem (3S, 3′S)‐Astaxanthin, seinem 15‐cis‐Isomeren und einigen analogen VerbindungenHelvetica Chimica Acta, 1977
- Synthese des (R)‐trans‐11‐Hydroxy‐8‐dodecensäure‐lactons (Recieifeiolid)Helvetica Chimica Acta, 1976
- Animal carotenoids: 7, 8-didehydroastaxanthin and 7, 8, 7′, 8′-tetradehydroastaxanthin from lobster eggsBiochemical Systematics and Ecology, 1976
- (3R,3′R)-astaxanthin from the yeast Phaffia rhodozymaPhytochemistry, 1976
- Synthese der enantiomeren 1,6‐Spiro[4.4]nonadieneHelvetica Chimica Acta, 1972
- The biosynthesis of astaxanthin. VI. the conversion of [14c]lutein and [14c] β-carotene in goldfishInternational Journal of Biochemistry, 1972
- The biosynthesis of astaxanthinInternational Journal of Biochemistry, 1970
- Über die Chiralität der enantiomeren Spiro[4.4]nonan‐1,6‐dioneHelvetica Chimica Acta, 1968