| Mualliflar | O. I. Fedorova, L. S. Morozova, Л. М. Алексеева, Г. С. Гриненко |
|---|---|
| Jurnal | Химия природных соединений |
| Nashriyot | Ўзбекистон Республикаси ФА |
| ISSN | 0009-3130, 1573-8388 |
| Nashr sanasi | 1983-07-01 |
| Jild | 19 |
| Son | 4 |
| Betlar | 437-440 |
| Til | Ingliz |
| Ilmiy soha | Farmatsevtika |
| DOI | 10.1007/bf00575701 |
| Indeksga qo‘shilgan | 2026-09-02 |
DOI: 10.1007/bf00575701 · Maqolaning asl sahifasi
| APA | O. I. Fedorova, L. S. Morozova, Л. М. Алексеева, & Г. С. Гриненко (1983). Preparation of 16-substituted 3-hydroxyestra-1,3,5(10)-triene-17-ones starting with the bromination of estrone acetate. Химия природных соединений, 19(4), 437-440. https://doi.org/10.1007/bf00575701 |
|---|---|
| GOST (OAK) | O. I. Fedorova va b. Preparation of 16-substituted 3-hydroxyestra-1,3,5(10)-triene-17-ones starting with the bromination of estrone acetate // Химия природных соединений. – 1983. – T. 19, № 4. – P. 437-440. – DOI: 10.1007/bf00575701. |
| MLA | O. I. Fedorova, L. S. Morozova, Л. М. Алексеева, and Г. С. Гриненко. “Preparation of 16-substituted 3-hydroxyestra-1,3,5(10)-triene-17-ones starting with the bromination of estrone acetate.” Химия природных соединений, 19(4), 437-440, 1983. https://doi.org/10.1007/bf00575701 |
| Chicago | O. I. Fedorova, L. S. Morozova, Л. М. Алексеева, and Г. С. Гриненко. “Preparation of 16-substituted 3-hydroxyestra-1,3,5(10)-triene-17-ones starting with the bromination of estrone acetate.” Химия природных соединений, 19(4), 437-440 (1983). https://doi.org/10.1007/bf00575701 |
| Harvard | O. I. Fedorova, L. S. Morozova, Л. М. Алексеева, and Г. С. Гриненко (1983) ‘Preparation of 16-substituted 3-hydroxyestra-1,3,5(10)-triene-17-ones starting with the bromination of estrone acetate’, Химия природных соединений, 19(4), 437-440. https://doi.org/10.1007/bf00575701 |
| BibTeX | @article{oifedorova1983,
title = {Preparation of 16-substituted 3-hydroxyestra-1,3,5(10)-triene-17-ones starting with the bromination of estrone acetate},
author = {O. I. Fedorova and L. S. Morozova and Л. М. Алексеева and Г. С. Гриненко},
journal = {Химия природных соединений},
year = {1983},
volume = {19},
number = {4},
pages = {437-440},
doi = {10.1007/bf00575701},
url = {https://doi.org/10.1007/bf00575701}
} |
Boshqa maqola uchun iqtibos tayyorlash
Химия природных соединений — barcha maqolalar · 1983-yil arxivi
The flavonoid content of green pea (Pisum sativum L.) seeds determined by HPLC was compared with data reported in the literature. Rutin (29.12 mg), quercetin (22.51 mg), luteolin (14.01 mg), dihydroquercetin (9.85 mg)…
The content of water-soluble vitamins (B1, B2, B3, B6, B9, PP, B12, C) in plant samples of the Cactaceae family was determined using the high-performance liquid chromatography (HPLC) method. The analyses were carried…
Obesity is one of the most prevalent chronic metabolic disorders worldwide and is strongly associated with an increased risk of type 2 diabetes mellitus, cardiovascular disease, arterial hypertension, and metabolic…
This study evaluated the antiradical activity of mixed chamomile and basil extracts prepared at different plant ratios and using different solvents. Chamomile-to-basil ratios of 1:1, 3:1, and 1:3 were extracted with…
This article evaluates the antiradical activity of onion (Allium cepa L.) and motherwort (Leonurus L.) plant extracts using the DPPH method. In the study, plant raw materials were mixed in mass ratios of 1:1, 3:1, and…
This article investigates the in vitro antiradical activity of four pomegranate varieties using a 2,2-diphenyl-1-picrylhydrazyl (DPPH) solution. The discoloration of the violet 2,2-diphenyl-1-picrylhydrazyl (DPPH)…