Мақаланы E-mail арқылы жіберу Hydroxyketones in the thiadiazine cycle formation
- Авторлар: Pulatov E.K.1, Isobaev M.J.1, Mavlonov B.G.1
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Мекемелер:
- V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Republic of Tajikistan
- Шығарылым: Том 65, № 10 (2016)
- Беттер: 2475-2478
- Бөлім: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/239187
- DOI: https://doi.org/10.1007/s11172-016-1609-3
- ID: 239187
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Аннотация
Cyclocondensation of 1-hydroxyketones with thiosemicarbazide resulted in thiadiazines. Nitrate ester of 1-hydroxyketone reacted under similar conditions to give the corresponding thiosemicarbazone. In the case of bromoacetyl-substituted nitrate ester of 1-hydroxyketone, condensation proceeded via intramolecular reaction between the thiol and bromomethyl groups.
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Авторлар туралы
E. Pulatov
V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Republic of Tajikistan
Хат алмасуға жауапты Автор.
Email: coordin@yandex.ru
Тәжікстан, 299/2 ul. Aini, Dushanbe, 734063
M. Isobaev
V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Republic of Tajikistan
Email: coordin@yandex.ru
Тәжікстан, 299/2 ul. Aini, Dushanbe, 734063
B. Mavlonov
V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Republic of Tajikistan
Email: coordin@yandex.ru
Тәжікстан, 299/2 ul. Aini, Dushanbe, 734063
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