dc.date.accessioned |
2019-01-22T20:40:26Z |
|
dc.date.available |
2019-01-22T20:40:26Z |
|
dc.date.issued |
2018 |
|
dc.identifier.issn |
1042-6507 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/148233 |
|
dc.description.abstract |
© 2018, © 2018 Taylor & Francis Group, LLC. The previously proposed mechanism for phospha-Michael addition of tertiary phosphines to electron-deficient alkenes has been amended according to the secondary kinetic isotope effects provided by α-deuterated activated alkenes. The data obtained have shown that rate-determining protonation of intermediate phosphonium zwitterion proceeds not directly at its carbanionic center but first at a heteroatom of the attached electron-withdrawing group, with subsequent isomerization of the enolic/eniminic intermediate to stable keto-/cyanophosphonium product. |
|
dc.relation.ispartofseries |
Phosphorus, Sulfur and Silicon and the Related Elements |
|
dc.subject |
kinetic isotope effects |
|
dc.subject |
Kinetics |
|
dc.subject |
mechanism |
|
dc.subject |
reactive intermediates |
|
dc.subject |
vibrational-rotational coupling |
|
dc.title |
Recent advances in studying the mechanism of phospha-Michael addition of tertiary phosphines to electron-deficient alkenes on the basis of kinetic isotope effects |
|
dc.type |
Article in Press |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.source.id |
SCOPUS10426507-2018-SID85058212695 |
|