Cleavage of P=O in the presence of P-N: aminophosphine oxide reduction with in situ boronation of the P(III) product.
about
First ever observation of the intermediate of phosphonium salt and ylide hydrolysis: P-hydroxytetraorganophosphorane.The Mechanism of Phosphonium Ylide Alcoholysis and Hydrolysis: Concerted Addition of the O-H Bond Across the P=C Bond.Chemoselective reduction of the phosphoryl bond of O-alkyl phosphinates and related compounds: an apparently impossible transformation.The Lightest Element Phosphoranylidene: NHC-Supported Cyclic Borylidene-Phosphorane with Significant B=P Character.
P2860
Cleavage of P=O in the presence of P-N: aminophosphine oxide reduction with in situ boronation of the P(III) product.
description
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name
Cleavage of P=O in the presenc ...... th in situ boronation of the P
@nl
Cleavage of P=O in the presenc ...... onation of the P(III) product.
@en
type
label
Cleavage of P=O in the presenc ...... th in situ boronation of the P
@nl
Cleavage of P=O in the presenc ...... onation of the P(III) product.
@en
prefLabel
Cleavage of P=O in the presenc ...... th in situ boronation of the P
@nl
Cleavage of P=O in the presenc ...... onation of the P(III) product.
@en
P2093
P2860
P356
P1476
Cleavage of P=O in the presenc ...... onation of the P(III) product.
@en
P2093
Declan G Gilheany
Elizabeth V Jennings
Kamalraj V Rajendran
Niall P Kenny
P2860
P304
14210-14214
P356
10.1002/CHEM.201302907
P407
P577
2013-09-11T00:00:00Z