Total synthesis of tropinone using 1,3-dipolar cycloaddition of cyclic azomethine ylide and phenyl vinyl sulfone as the key step

Joydev K. Laha

Химия природных соединений · 2010-yil

Maqola ma’lumotlari
MualliflarJoydev K. Laha
JurnalХимия природных соединений
NashriyotЎзбекистон Республикаси ФА
ISSN0009-3130, 1573-8388
Nashr sanasi2010-05-01
Jild46
Son2
Betlar254-256
TilIngliz
Ilmiy sohaKimyo
DOI10.1007/s10600-010-9581-x
Indeksga qo‘shilgan2026-09-02

Ilmiy soha

Iqtibos keltirish

APAJoydev K. Laha (2010). Total synthesis of tropinone using 1,3-dipolar cycloaddition of cyclic azomethine ylide and phenyl vinyl sulfone as the key step. Химия природных соединений, 46(2), 254-256. https://doi.org/10.1007/s10600-010-9581-x
GOST (OAK)Joydev K. Laha Total synthesis of tropinone using 1,3-dipolar cycloaddition of cyclic azomethine ylide and phenyl vinyl sulfone as the key step // Химия природных соединений. – 2010. – T. 46, № 2. – P. 254-256. – DOI: 10.1007/s10600-010-9581-x.
MLAJoydev K. Laha. “Total synthesis of tropinone using 1,3-dipolar cycloaddition of cyclic azomethine ylide and phenyl vinyl sulfone as the key step.” Химия природных соединений, 46(2), 254-256, 2010. https://doi.org/10.1007/s10600-010-9581-x
ChicagoJoydev K. Laha. “Total synthesis of tropinone using 1,3-dipolar cycloaddition of cyclic azomethine ylide and phenyl vinyl sulfone as the key step.” Химия природных соединений, 46(2), 254-256 (2010). https://doi.org/10.1007/s10600-010-9581-x
HarvardJoydev K. Laha (2010) ‘Total synthesis of tropinone using 1,3-dipolar cycloaddition of cyclic azomethine ylide and phenyl vinyl sulfone as the key step’, Химия природных соединений, 46(2), 254-256. https://doi.org/10.1007/s10600-010-9581-x
BibTeX
@article{joydevklaha2010,
  title = {Total synthesis of tropinone using 1,3-dipolar cycloaddition of cyclic azomethine ylide and phenyl vinyl sulfone as the key step},
  author = {Joydev K. Laha},
  journal = {Химия природных соединений},
  year = {2010},
  volume = {46},
  number = {2},
  pages = {254-256},
  doi = {10.1007/s10600-010-9581-x},
  url = {https://doi.org/10.1007/s10600-010-9581-x}
}

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