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TOTAL SYNTHESIS OF dl-19-NOR-16,17-DEHYDROPROGESTERONE
dl-2-(7,11-Dimethyl-3,7,11 - trans,trans-dodecatrienyl)-3-methyl-cyclopent-2-enol was prepared by reduction of the corresponding ketone. This tetraenol, on treatment with trifluoroacetic acid, underwent stereoselective cyclization to give dl-3,17-dimethyl-A-nor-D-homoestra-3,16-diene. This tetracycl...
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| Опубликовано в: : | Proc Natl Acad Sci U S A |
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| Главные авторы: | , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
National Academy of Sciences
1969
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC277793/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/5256214/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.62.2.333 |
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