56372-47-5Relevant articles and documents
A Catalyst-Free Synthesis of Phosphinic Amides Using O-Benzoylhydroxylamines
Zhu, Rui,Pan, Chongqing,Gu, Zhenhua
supporting information, p. 5862 - 5865 (2015/12/11)
A practical approach for the synthesis of phosphinic amides via the coupling of secondary phosphine oxides (SPOs) with O-benzoylhydroxylamines has been reported. Simply heating the mixture of SPOs and O-benzoylhydroxylamines in the presence of K2/su
The reactivity of arylphosphorus acid amides under Birch reduction conditions
Stankevic, Marek,Wlodarczyk, Adam,Nieckarz, Damian
, p. 4351 - 4371 (2013/07/26)
Several classes of arylphosphorus acid amides have been tested in reactions with alkali metal solutions in liquid ammonia. The outcomes of such reactions depend on the structures of the starting materials. Generally, two processes-Birch reduction or cleavage of the P-aryl bond-can be operative. Diarylphosphinic amides tend to undergo double Birch reduction to afford bis(cyclohexadienyl)phosphinic amides. Copyright
Efficient amidation and esterification of phosphoric acid using Cl 3CCN/ Ph3P
Kasemsuknimit, Atthapol,Satyender, Apuri,Chavasiri, Warinthorn,Jang, Doo Ok
scheme or table, p. 3486 - 3488 (2012/01/13)
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