Форма представления | Статьи в зарубежных журналах и сборниках |
Год публикации | 2021 |
Язык | английский |
|
Павельев Роман Сергеевич, автор
|
Библиографическое описание на языке оригинала |
Sapozhnikov S.V, Pavelyev R.S, Shtyrlin N.V, Synthetic route optimization of pyridosept antiseptic drug candidate//AIP Conference Proceedings. - 2021. - Vol.2388, Is.. - Art. №030040. |
Аннотация |
In this work we have described the transformation of synthetic route of the antiseptic drug candidate Pyridosept. Initial method has included in seven steps and has poor overall yield of target compound. This is the convenient developing process, scalable and technologi. The overall yield was increased up to 22% in four steps without column chromatography purification which allows to obtain the target compound with purity of 99.5+% which is especially important for the active ingredient. |
Ключевые слова |
pyridoxine, vitamin B6, antiseptic |
Название журнала |
AIP Conference Proceedings
|
URL |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85120410305&doi=10.1063%2f5.0068420&partnerID=40&md5=d35907ab35f3080ef4a200cb123f35d2 |
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https://repository.kpfu.ru/?p_id=261926 |
Полная запись метаданных ![](https://shelly.kpfu.ru/pdf/picture/arrow_black_right.gif) |
Поле DC |
Значение |
Язык |
dc.contributor.author |
Павельев Роман Сергеевич |
ru_RU |
dc.date.accessioned |
2021-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2021-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2021 |
ru_RU |
dc.identifier.citation |
Sapozhnikov S.V, Pavelyev R.S, Shtyrlin N.V, Synthetic route optimization of pyridosept antiseptic drug candidate//AIP Conference Proceedings. - 2021. - Vol.2388, Is.. - Art. №030040. |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/?p_id=261926 |
ru_RU |
dc.description.abstract |
AIP Conference Proceedings |
ru_RU |
dc.description.abstract |
In this work we have described the transformation of synthetic route of the antiseptic drug candidate Pyridosept. Initial method has included in seven steps and has poor overall yield of target compound. This is the convenient developing process, scalable and technologi. The overall yield was increased up to 22% in four steps without column chromatography purification which allows to obtain the target compound with purity of 99.5+% which is especially important for the active ingredient. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
pyridoxine |
ru_RU |
dc.subject |
vitamin B6 |
ru_RU |
dc.subject |
antiseptic |
ru_RU |
dc.title |
Synthetic route optimization of pyridosept antiseptic drug candidate |
ru_RU |
dc.type |
Статьи в зарубежных журналах и сборниках |
ru_RU |
|