Form of presentation | Articles in Russian journals and collections |
Year of publication | 2017 |
Язык | английский |
|
Mironov Vladimir Fedorovich, author
Nemtarev Andrey Vladimirovich, author
|
|
Shemakhina Mariya Eduardovna, author
|
Bibliographic description in the original language |
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. |
Annotation |
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. |
Keywords |
pulegone, methyl dichlorophosphite, phosphorylation, oxaphospholene, phosphoryl ketones, oxoalkylphosphonates |
The name of the journal |
Russian Journal of General Chemistry
|
URL |
https://link.springer.com/article/10.1134/S1070363217040387 |
Please use this ID to quote from or refer to the card |
https://repository.kpfu.ru/eng/?p_id=174862&p_lang=2 |
Full metadata record |
Field DC |
Value |
Language |
dc.contributor.author |
Mironov Vladimir Fedorovich |
ru_RU |
dc.contributor.author |
Nemtarev Andrey Vladimirovich |
ru_RU |
dc.contributor.author |
Shemakhina Mariya Eduardovna |
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/eng/?p_id=174862&p_lang=2 |
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 |
Articles in Russian journals and collections |
ru_RU |
|