Форма представления | Статьи в российских журналах и сборниках |
Год публикации | 2017 |
Язык | английский |
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Миронов Владимир Федорович, автор
Немтарев Андрей Владимирович, автор
|
|
Шемахина Мария Эдуардовна, автор
|
Библиографическое описание на языке оригинала |
A.V.Nemtarev, M.E.Shemakhina, V.F.Mironov. 3,3,6-Trimethyl-2-chlorocyclohexeno[1,2-d]-1,2-oxaphosphol-4-ene-2-oxide as a convenient precursor for the synthesis of dimephosphone analogs. // Russ. J. Gen. Chem. 2017. Vol. 87. No. 4. P. 887-889. Doi 10.1134/S1070363217040387. |
Аннотация |
A convenient approach to the synthesis of 3,3,6-trimethyl-2-chlorocyclohexeno[1,2-d]-1,2-oxaphosphol-3-ene-2-oxide was developed based on the reaction of the naturally occurring terpenoketone pulegone with methyl dichlorophosphite. Treatment of oxaphospholene-2-oxide with water or ethanol yielded γ-phosphoryl ketones, dimephosphone analogs. The studied hydrolysis and alcoholysis processes differ in stereoselectivity. |
Ключевые слова |
pulegone, methyl dichlorophosphite, phosphorylation, oxaphospholene, phosphoryl ketones, oxoalkylphosphonates |
Название журнала |
Russian Journal of General Chemistry
|
URL |
https://link.springer.com/article/10.1134/S1070363217040387 |
Пожалуйста, используйте этот идентификатор, чтобы цитировать или ссылаться на эту карточку |
https://repository.kpfu.ru/?p_id=174862 |
Полная запись метаданных |
Поле DC |
Значение |
Язык |
dc.contributor.author |
Миронов Владимир Федорович |
ru_RU |
dc.contributor.author |
Немтарев Андрей Владимирович |
ru_RU |
dc.contributor.author |
Шемахина Мария Эдуардовна |
ru_RU |
dc.date.accessioned |
2017-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2017-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2017 |
ru_RU |
dc.identifier.citation |
A.V.Nemtarev, M.E.Shemakhina, V.F.Mironov. 3,3,6-Trimethyl-2-chlorocyclohexeno[1,2-d]-1,2-oxaphosphol-4-ene-2-oxide as a convenient precursor for the synthesis of dimephosphone analogs. // Russ. J. Gen. Chem. 2017. Vol. 87. No. 4. P. 887-889. Doi 10.1134/S1070363217040387. |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/?p_id=174862 |
ru_RU |
dc.description.abstract |
Russian Journal of General Chemistry |
ru_RU |
dc.description.abstract |
A convenient approach to the synthesis of 3,3,6-trimethyl-2-chlorocyclohexeno[1,2-d]-1,2-oxaphosphol-3-ene-2-oxide was developed based on the reaction of the naturally occurring terpenoketone pulegone with methyl dichlorophosphite. Treatment of oxaphospholene-2-oxide with water or ethanol yielded γ-phosphoryl ketones, dimephosphone analogs. The studied hydrolysis and alcoholysis processes differ in stereoselectivity. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
pulegone |
ru_RU |
dc.subject |
methyl dichlorophosphite |
ru_RU |
dc.subject |
phosphorylation |
ru_RU |
dc.subject |
oxaphospholene |
ru_RU |
dc.subject |
phosphoryl ketones |
ru_RU |
dc.subject |
oxoalkylphosphonates |
ru_RU |
dc.title |
3,3,6-Trimethyl-2-chlorocyclohexeno[1,2-d]-1,2-oxaphosphol-4-ene-2-oxide as a convenient precursor for the synthesis of dimephosphone analogs |
ru_RU |
dc.type |
Статьи в российских журналах и сборниках |
ru_RU |
|