Synthesis and biological activity of 3,4-dihydropyrimidin-2-thione aminomethylene derivatives based on the alkaloid cytisine

И. В. Кулаков

Химия природных соединений · 2011-yil

Maqola ma’lumotlari
MualliflarИ. В. Кулаков
JurnalХимия природных соединений
NashriyotЎзбекистон Республикаси ФА
ISSN0009-3130, 1573-8388
Nashr sanasi2011-09-01
Jild47
Son4
Betlar597-599
TilIngliz
Ilmiy sohaKimyo
DOI10.1007/s10600-011-0004-4
Indeksga qo‘shilgan2026-09-02

DOI: 10.1007/s10600-011-0004-4 · Maqolaning asl sahifasi

Ilmiy soha

Kimyo

Iqtibos keltirish

APAИ. В. Кулаков (2011). Synthesis and biological activity of 3,4-dihydropyrimidin-2-thione aminomethylene derivatives based on the alkaloid cytisine. Химия природных соединений, 47(4), 597-599. https://doi.org/10.1007/s10600-011-0004-4
GOST (OAK)И. В. Кулаков Synthesis and biological activity of 3,4-dihydropyrimidin-2-thione aminomethylene derivatives based on the alkaloid cytisine // Химия природных соединений. – 2011. – T. 47, № 4. – P. 597-599. – DOI: 10.1007/s10600-011-0004-4.
MLAИ. В. Кулаков. “Synthesis and biological activity of 3,4-dihydropyrimidin-2-thione aminomethylene derivatives based on the alkaloid cytisine.” Химия природных соединений, 47(4), 597-599, 2011. https://doi.org/10.1007/s10600-011-0004-4
ChicagoИ. В. Кулаков. “Synthesis and biological activity of 3,4-dihydropyrimidin-2-thione aminomethylene derivatives based on the alkaloid cytisine.” Химия природных соединений, 47(4), 597-599 (2011). https://doi.org/10.1007/s10600-011-0004-4
HarvardИ. В. Кулаков (2011) ‘Synthesis and biological activity of 3,4-dihydropyrimidin-2-thione aminomethylene derivatives based on the alkaloid cytisine’, Химия природных соединений, 47(4), 597-599. https://doi.org/10.1007/s10600-011-0004-4
BibTeX
@article{article2011,
  title = {Synthesis and biological activity of 3,4-dihydropyrimidin-2-thione aminomethylene derivatives based on the alkaloid cytisine},
  author = {И. В. Кулаков},
  journal = {Химия природных соединений},
  year = {2011},
  volume = {47},
  number = {4},
  pages = {597-599},
  doi = {10.1007/s10600-011-0004-4},
  url = {https://doi.org/10.1007/s10600-011-0004-4}
}

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