dc.contributor.author |
Khusainova N. |
|
dc.contributor.author |
Mostovaya O. |
|
dc.contributor.author |
Berdnikov E. |
|
dc.contributor.author |
Efremov Y. |
|
dc.contributor.author |
Sharafutdinova D. |
|
dc.contributor.author |
Cherkasov R. |
|
dc.date.accessioned |
2018-09-17T21:17:54Z |
|
dc.date.available |
2018-09-17T21:17:54Z |
|
dc.date.issued |
2004 |
|
dc.identifier.issn |
1066-5285 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/134803 |
|
dc.description.abstract |
The reaction of 1,2-ethanedithiol with diethyl vinylphosphonate in the presence of EtONa occurs as the addition of the sulfhydryl group to the β-carbon atom of the substrate to give 1:1 and 1:2 adducts. The nucleophilic addition of 2-mercaptoethanol at the β position of the multiple bond of diethyl vinyl-, diethyl allenyl-, and diethyl prop-1-ynylphosphonates involves only the sulfhydryl group. © 2004 Springer Science+Business Media, Inc. |
|
dc.relation.ispartofseries |
Russian Chemical Bulletin |
|
dc.subject |
1,2-ethanedithiol |
|
dc.subject |
2-mercaptoethanol |
|
dc.subject |
Diethyl allenylphosphonate |
|
dc.subject |
Diethyl prop-1-ynylphosphonate |
|
dc.subject |
Diethyl vinylphosphonate |
|
dc.subject |
Functionalization |
|
dc.subject |
Nucleophilic addition |
|
dc.title |
Reactions of 1,2-ethanedithiol and 2-mercaptoethanol with unsaturated derivatives of four-coordinate phosphorus acids |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
10 |
|
dc.relation.ispartofseries-volume |
53 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
2253 |
|
dc.source.id |
SCOPUS10665285-2004-53-10-SID21644474461 |
|