Zur Konfiguration des Vitamin‐D3‐Metaboliten 25, 26‐Dihydroxycholecalciferol: Synthese von (25S,26)‐ und (25R,26)‐Dihydroxycholecalciferol
- 29 April 1981
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 64 (3) , 915-938
- https://doi.org/10.1002/hlca.19810640328
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- The absolute configuration of the natural 26,26‐dihydroxycholecalciferolFEBS Letters, 1980
- The configuration at C‐25 of human 25,26‐dihydroxycholecalciferolFEBS Letters, 1979
- Totalsynthese von natürlichem α‐Tocopherol. 4. Mitteilung. Aufbau des Chromanringsystems aus Trimethylhydrochinon und einem optisch aktiven C4‐ bzw. C5‐SynthonHelvetica Chimica Acta, 1979
- The absolute configuration of the natural 25,26‐dihydroxycholecalciferolFEBS Letters, 1978
- Pairs inP21: probability distributions which lead to estimates of the two-phase structure seminvariants in the vicinity of ±π/2Acta Crystallographica Section A, 1978
- A synthesis of the ophiobolin nucleusThe Journal of Organic Chemistry, 1977
- Vitamin D3 Metabolites I. Synthesis of 25‐hydroxycholesterolHelvetica Chimica Acta, 1974
- Vitamin D, example and challengeCellular and Molecular Life Sciences, 1973
- Tris[3-(trifluoromethylhydroxymethylene)-d-camphorato]europium(III). Chiral shift reagent for direct determination of enantiomeric compositionsJournal of the American Chemical Society, 1971
- The application of phase relationships to complex structures. III. The optimum use of phase relationshipsActa Crystallographica Section A, 1971