The synthesis of 8-methyl-PGC22 and 12-methyl-PGAa3 and -PGE24 has been described recently. Degradation to biological inactive PGB-derivatives 1s lmpossible in these compounds. We now wish to report the synthesis of the lO,lO-dimethyl-PGEl analog A, which cannot be deactivated easily by transformat
โฆ LIBER โฆ
Synthesis of 10,10-dimethylprostaglandin F1 and F2 analogues
โ Scribed by O. G. Plantema; H. de Koning; H. O. Huisman
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 772 KB
- Volume
- 102
- Category
- Article
- ISSN
- 0165-0513
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