© 2016 Taylor & Francis Group, LLC.The Michael-type addition of tertiary phosphines to electron-deficient alkenes is a convenient way to generate reactive phosphonium zwitterionic intermediates, which participate readily in many synthetically useful transformations. Although the synthetic usefulness of the phospha–Michael addition has been largely demonstrated, knowledge on the kinetics and mechanism of this reaction is sparse. This paper briefly summarizes the contribution of our research group to find out the mechanism of this reaction
The structures of intermediates and transition states in the reaction of tertiary phosphines with un...
The kinetics of the reactions of tributylphosphine with allenic and olefinic Michael acceptors in di...
The kinetics of the reactions of tributylphosphine with allenic and olefinic Michael acceptors in di...
© 2016 Taylor & Francis Group, LLC.The Michael-type addition of tertiary phosphines to electron-defi...
© 2016 Taylor & Francis Group, LLC.The Michael-type addition of tertiary phosphines to electron-defi...
© 2018, © 2018 Taylor & Francis Group, LLC. The previously proposed mechanism for phospha-Michael ...
© 2018, © 2018 Taylor & Francis Group, LLC. The previously proposed mechanism for phospha-Michael ...
Kinetic data provide evidence that proton transfer to the carbanion centre of a phosphonium zwitteri...
Kinetic data provide evidence that proton transfer to the carbanion centre of a phosphonium zwitteri...
Kinetic data provide evidence that proton transfer to the carbanion centre of a phosphonium zwitteri...
Kinetic data provide evidence that proton transfer to the carbanion centre of a phosphonium zwitteri...
© 2016 Bentham Science Publishers.Conjugate addition of dialkyl phosphites and ethyl phenylphosphina...
© 2016 Taylor & Francis Group, LLC.Conjugate addition of diisobutyl phosphite to activated alkenes u...
Data obtained while studying the kinetics of quaternization of tertiary phosphines with the unsatura...
The kinetics of the reaction of tertiary phosphines with acrylic acid in a series of aprotic solvent...
The structures of intermediates and transition states in the reaction of tertiary phosphines with un...
The kinetics of the reactions of tributylphosphine with allenic and olefinic Michael acceptors in di...
The kinetics of the reactions of tributylphosphine with allenic and olefinic Michael acceptors in di...
© 2016 Taylor & Francis Group, LLC.The Michael-type addition of tertiary phosphines to electron-defi...
© 2016 Taylor & Francis Group, LLC.The Michael-type addition of tertiary phosphines to electron-defi...
© 2018, © 2018 Taylor & Francis Group, LLC. The previously proposed mechanism for phospha-Michael ...
© 2018, © 2018 Taylor & Francis Group, LLC. The previously proposed mechanism for phospha-Michael ...
Kinetic data provide evidence that proton transfer to the carbanion centre of a phosphonium zwitteri...
Kinetic data provide evidence that proton transfer to the carbanion centre of a phosphonium zwitteri...
Kinetic data provide evidence that proton transfer to the carbanion centre of a phosphonium zwitteri...
Kinetic data provide evidence that proton transfer to the carbanion centre of a phosphonium zwitteri...
© 2016 Bentham Science Publishers.Conjugate addition of dialkyl phosphites and ethyl phenylphosphina...
© 2016 Taylor & Francis Group, LLC.Conjugate addition of diisobutyl phosphite to activated alkenes u...
Data obtained while studying the kinetics of quaternization of tertiary phosphines with the unsatura...
The kinetics of the reaction of tertiary phosphines with acrylic acid in a series of aprotic solvent...
The structures of intermediates and transition states in the reaction of tertiary phosphines with un...
The kinetics of the reactions of tributylphosphine with allenic and olefinic Michael acceptors in di...
The kinetics of the reactions of tributylphosphine with allenic and olefinic Michael acceptors in di...