Synthesis and calming activity of 6H-2-Amino-4-Aryl-6-(4-β-D-Allopyranosyloxyphenyl)-1,3-Thiazine

Li Fu, Ye Ding, Ying Li, Shufan Yin

Химия природных соединений · 2010-yil

Maqola ma’lumotlari
MualliflarLi Fu, Ye Ding, Ying Li, Shufan Yin
JurnalХимия природных соединений
NashriyotЎзбекистон Республикаси ФА
ISSN0009-3130, 1573-8388
Nashr sanasi2010-05-01
Jild46
Son2
Betlar169-172
TilIngliz
Ilmiy sohaKimyo
DOI10.1007/s10600-010-9559-8
Indeksga qo‘shilgan2026-09-02

DOI: 10.1007/s10600-010-9559-8 · Maqolaning asl sahifasi

Ilmiy soha

Kimyo

Iqtibos keltirish

APALi Fu, Ye Ding, Ying Li, & Shufan Yin (2010). Synthesis and calming activity of 6H-2-Amino-4-Aryl-6-(4-β-D-Allopyranosyloxyphenyl)-1,3-Thiazine. Химия природных соединений, 46(2), 169-172. https://doi.org/10.1007/s10600-010-9559-8
GOST (OAK)Li Fu va b. Synthesis and calming activity of 6H-2-Amino-4-Aryl-6-(4-β-D-Allopyranosyloxyphenyl)-1,3-Thiazine // Химия природных соединений. – 2010. – T. 46, № 2. – P. 169-172. – DOI: 10.1007/s10600-010-9559-8.
MLALi Fu, Ye Ding, Ying Li, and Shufan Yin. “Synthesis and calming activity of 6H-2-Amino-4-Aryl-6-(4-β-D-Allopyranosyloxyphenyl)-1,3-Thiazine.” Химия природных соединений, 46(2), 169-172, 2010. https://doi.org/10.1007/s10600-010-9559-8
ChicagoLi Fu, Ye Ding, Ying Li, and Shufan Yin. “Synthesis and calming activity of 6H-2-Amino-4-Aryl-6-(4-β-D-Allopyranosyloxyphenyl)-1,3-Thiazine.” Химия природных соединений, 46(2), 169-172 (2010). https://doi.org/10.1007/s10600-010-9559-8
HarvardLi Fu, Ye Ding, Ying Li, and Shufan Yin (2010) ‘Synthesis and calming activity of 6H-2-Amino-4-Aryl-6-(4-β-D-Allopyranosyloxyphenyl)-1,3-Thiazine’, Химия природных соединений, 46(2), 169-172. https://doi.org/10.1007/s10600-010-9559-8
BibTeX
@article{lifu2010,
  title = {Synthesis and calming activity of 6H-2-Amino-4-Aryl-6-(4-β-D-Allopyranosyloxyphenyl)-1,3-Thiazine},
  author = {Li Fu and Ye Ding and Ying Li and Shufan Yin},
  journal = {Химия природных соединений},
  year = {2010},
  volume = {46},
  number = {2},
  pages = {169-172},
  doi = {10.1007/s10600-010-9559-8},
  url = {https://doi.org/10.1007/s10600-010-9559-8}
}

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