Add to ORKG© 2016 Taylor & Francis Group, LLC.Conjugate addition of diisobutyl phosphite to activated alkenes under PBu3 catalysis affords corresponding phosphonates in high yields within short reaction times
The hydrophosphination of carbon-carbon multiple bonds has been generally performed under acid, base...
We carried out a comprehensive study on the generality, scope, limitations, and mechanism of the pal...
We carried out a comprehensive study on the generality, scope, limitations, and mechanism of the pal...
© 2016 Taylor & Francis Group, LLC.Conjugate addition of diisobutyl phosphite to activated alkenes u...
© 2016 Taylor & Francis Group, LLC.Conjugate addition of diisobutyl phosphite to activated alkenes u...
© 2016 Taylor & Francis Group, LLC.Conjugate addition of diisobutyl phosphite to activated alkenes u...
© 2016 Bentham Science Publishers.Conjugate addition of dialkyl phosphites and ethyl phenylphosphina...
© 2016 Bentham Science Publishers.Conjugate addition of dialkyl phosphites and ethyl phenylphosphina...
© 2016 Taylor & Francis Group, LLC.The Michael-type addition of tertiary phosphines to electron-defi...
© 2015 Elsevier Ltd. An efficient PBu3-catalyzed α-addition of the P(O)-H bond to ethyl phenylpropio...
© 2015 Elsevier Ltd. An efficient PBu3-catalyzed α-addition of the P(O)-H bond to ethyl phenylpropio...
© 2015 Elsevier Ltd. An efficient PBu3-catalyzed α-addition of the P(O)-H bond to ethyl phenylpropio...
© 2015 Elsevier Ltd. An efficient PBu3-catalyzed α-addition of the P(O)-H bond to ethyl phenylpropio...
The hydrophosphination of carbon–carbon multiple bonds has been generally performed under acid, base...
We carried out a comprehensive study on the generality, scope, limitations, and mechanism of the pal...
The hydrophosphination of carbon-carbon multiple bonds has been generally performed under acid, base...
We carried out a comprehensive study on the generality, scope, limitations, and mechanism of the pal...
We carried out a comprehensive study on the generality, scope, limitations, and mechanism of the pal...
© 2016 Taylor & Francis Group, LLC.Conjugate addition of diisobutyl phosphite to activated alkenes u...
© 2016 Taylor & Francis Group, LLC.Conjugate addition of diisobutyl phosphite to activated alkenes u...
© 2016 Taylor & Francis Group, LLC.Conjugate addition of diisobutyl phosphite to activated alkenes u...
© 2016 Bentham Science Publishers.Conjugate addition of dialkyl phosphites and ethyl phenylphosphina...
© 2016 Bentham Science Publishers.Conjugate addition of dialkyl phosphites and ethyl phenylphosphina...
© 2016 Taylor & Francis Group, LLC.The Michael-type addition of tertiary phosphines to electron-defi...
© 2015 Elsevier Ltd. An efficient PBu3-catalyzed α-addition of the P(O)-H bond to ethyl phenylpropio...
© 2015 Elsevier Ltd. An efficient PBu3-catalyzed α-addition of the P(O)-H bond to ethyl phenylpropio...
© 2015 Elsevier Ltd. An efficient PBu3-catalyzed α-addition of the P(O)-H bond to ethyl phenylpropio...
© 2015 Elsevier Ltd. An efficient PBu3-catalyzed α-addition of the P(O)-H bond to ethyl phenylpropio...
The hydrophosphination of carbon–carbon multiple bonds has been generally performed under acid, base...
We carried out a comprehensive study on the generality, scope, limitations, and mechanism of the pal...
The hydrophosphination of carbon-carbon multiple bonds has been generally performed under acid, base...
We carried out a comprehensive study on the generality, scope, limitations, and mechanism of the pal...
We carried out a comprehensive study on the generality, scope, limitations, and mechanism of the pal...