An efficient procedure for the synthesis and isolation of (+)-(2R,3R,11R,12R)- and (−)-(2S,3S,11S,12S)-tetraphenyl-18-crown-6
✍ Scribed by John Crosby; Martin E. Fakley; Colin Gemmell; Keith Martin; Andrew Quick; Alexandra M.Z. Slawin; Hooshang Shahriari-Zavareh; J. Fraser Stoddart; David J. Williams
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 326 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
octadecanes have been preparedin single step reactions from the readily-available chiralprecursors, (RR)-and (5%).hydrobenzoins, followed by bulk isolations of the pure Id-crown-6 derivatives via their I.9 crystalline complexes with potassium nitrate (for the Uiphenyl derivative) or calcium nitrate (for the tetraphenyl derivative), obtaineddirectly from the worked-up crude reaction mixtures: X-ray crystal structures character&e the uncomplexed (RRRR)tetraphenyi-l&crown-6 and the 1 :I complex formed between its (SSSS)-enantiomer and calcium nitrate.
📜 SIMILAR VOLUMES
Plakoside A (1) is a prenylated galactosphingolipid isolated from the marine sponge Plakortis simplex and is strongly immunosuppressive without cytotoxicity. (2S,3R,11S,12R,2 §R,11 §S,12 §R)-plakoside A (1) was synthesized by combining sphingosine part 16, a-hydroxy acid part 24 and prenylated sugar
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