Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Albert R. Fatkhutdinov"'
Publikováno v:
International Journal of Chemical Kinetics. 48:161-168
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65380cb7fc7ace28471a3e84401e1451
https://doi.org/10.1002/kin.20981
https://doi.org/10.1002/kin.20981
Autor:
Daut R. Islamov, Vladimir I. Galkin, Olga N. Kataeva, Fanuza G. Shamsutdinova, Anton V. Il, Albert R. Fatkhutdinov, Alexey V. Salin
Publikováno v:
Current Organic Synthesis. 13:132-141
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58eaca64976e3332a0993e1211df0b5f
https://doi.org/10.2174/1570179412999150723154625
https://doi.org/10.2174/1570179412999150723154625
Autor:
Alexey V. Salin, Daut R. Islamov, Anton V. Il'in, Vladimir I. Galkin, Albert R. Fatkhutdinov, Olga N. Kataeva, Fanuza G. Shamsutdinova
Publikováno v:
Tetrahedron Letters. 56:6282-6286
An efficient PBu3-catalyzed α-addition of the P(O)–H bond to ethyl phenylpropiolate has been developed. This strategy offers a facile method for the preparation of synthetically useful alkenyl phosphonates and phosphinates proceeding under neutral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07b9110f4e26944423ebfef54b434f07
https://doi.org/10.1016/j.tetlet.2015.09.137
https://doi.org/10.1016/j.tetlet.2015.09.137
Autor:
Albert R. Fatkhutdinov, Vladimir I. Galkin, Anton V. II'in, Fanuza G. Shamsutdinova, Alexey V. Salin
Publikováno v:
Heteroatom Chemistry. 25:205-216
In aprotic solvents, kinetics of the reaction of triphenylphosphine with acrylic acid is second order in the acid and first order in the phosphine. To find the most suitable model to describe the solvent effect on this reaction, the third-order rate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea009ec602b757aa801853a15fe79d70
https://doi.org/10.1002/hc.21161
https://doi.org/10.1002/hc.21161
Publikováno v:
International Journal of Chemical Kinetics. 46:206-215
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da2c856a3a360e634865d1c8f9aaf06c
https://doi.org/10.1002/kin.20842
https://doi.org/10.1002/kin.20842
Autor:
A. A. Sobanov, Alexey V. Salin, Vladimir I. Galkin, Albert R. Fatkhutdinov, Anton V. Il'in, Evgeniy I. Sotov, Brian R. James
Publikováno v:
Journal of Physical Organic Chemistry. 26:675-678
Kinetic data provide evidence that proton transfer to the carbanion centre of a phosphonium zwitterion is the rate-determining step in quarternization reactions of triphenylphosphine with electron-deficient alkenes in acetic acid solution. This concl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8e93bd16ea3eb3374220192244bf4fb
https://doi.org/10.1002/poc.3154
https://doi.org/10.1002/poc.3154
Autor:
Olga N. Kataeva, Daut R. Islamov, Anton V. Il'in, Vladimir I. Galkin, Albert R. Fatkhutdinov, Alexey V. Salin, Fanuza G. Shamsutdinova
Publikováno v:
ChemInform. 47
An efficient PBu3-catalyzed α-addition of the P(O)–H bond to ethyl phenylpropiolate has been developed. This strategy offers a facile method for the preparation of synthetically useful alkenyl phosphonates and phosphinates proceeding under neutral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d972dab492805c59a611bec9227b607
https://doi.org/10.1002/chin.201608204
https://doi.org/10.1002/chin.201608204
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 191:1628-1629
Conjugate addition of diisobutyl phosphite to activated alkenes under PBu3 catalysis affords corresponding phosphonates in high yields within short reaction times.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90725c3c93c6873f39344b4ba84df2da
https://doi.org/10.1080/10426507.2016.1223657
https://doi.org/10.1080/10426507.2016.1223657