Товарлар кимёси ва халқ табобати 2-том 2-нөмір (2023) · 24-43-беттер

SEPARATION OF RACEMIC 3-METHYL-3-AMINOPENTINE-1 TO OPTICALLY ACTIVE ANTIPODES BY DIASTEREOMERIZATION

Abdullaev, Takhir Kh., Isobaev, Muzafar D., Askarov, Ibragim R., Abdulloev, Obidjon Sh.

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Аңдатпа

The article presents the results of studies on the separation of racemic 3-methyl-3-aminopentine-1 of their derivatives into optically active antipodes by diastereomerization using by L–(+)-tartaric acid. The structures of the obtained compounds established by uzing IR and NMR spectroscopy.

Оптически активные аминыдиастереомерная сольэнантиомерыквантовохимические расчетыконформационный анализПМРИК-спектроскопияOptically active aminesdiastereomeric saltenantiomers

Метадеректер дереккөзі: журналдың OAI-PMH архиві · Sindex толық мәтінді сақтамайды, дереккөзге сілтеме береді.

Дәйексөз алу

APA 7 
Abdullaev, Takhir Kh., Isobaev, Muzafar D., Askarov, Ibragim R. & Abdulloev, Obidjon Sh. (2023). SEPARATION OF RACEMIC 3-METHYL-3-AMINOPENTINE-1 TO OPTICALLY ACTIVE ANTIPODES BY DIASTEREOMERIZATION. Товарлар кимёси ва халқ табобати, 2(2), 24-43.
GOST R 7.0.5 
Abdullaev, Takhir Kh., Isobaev, Muzafar D., Askarov, Ibragim R., Abdulloev, Obidjon Sh. SEPARATION OF RACEMIC 3-METHYL-3-AMINOPENTINE-1 TO OPTICALLY ACTIVE ANTIPODES BY DIASTEREOMERIZATION // Товарлар кимёси ва халқ табобати. 2023. Т. 2. № 2. С. 24-43.
BibTeX 
@article{kh.2023,
  author  = {Abdullaev, Takhir Kh. and Isobaev, Muzafar D. and Askarov, Ibragim R. and Abdulloev, Obidjon Sh.},
  title   = {SEPARATION OF RACEMIC 3-METHYL-3-AMINOPENTINE-1 TO OPTICALLY ACTIVE ANTIPODES BY DIASTEREOMERIZATION},
  journal = {Товарлар кимёси ва халқ табобати},
  year    = {2023},
  volume  = {2},
  number  = {2},
  pages   = {24-43}
}
RIS 
TY  - JOUR
AU  - Abdullaev, Takhir Kh.
AU  - Isobaev, Muzafar D.
AU  - Askarov, Ibragim R.
AU  - Abdulloev, Obidjon Sh.
TI  - SEPARATION OF RACEMIC 3-METHYL-3-AMINOPENTINE-1 TO OPTICALLY ACTIVE ANTIPODES BY DIASTEREOMERIZATION
JO  - Товарлар кимёси ва халқ табобати
PY  - 2023
VL  - 2
IS  - 2
SP  - 24
EP  - 43
ER  -