90609-99-7Relevant academic research and scientific papers
N-substituted aminomethanephosphonic and aminomethane-P-methylphosphinic acids as inhibitors of ureases
Berlicki, Lukasz,Bochno, Marta,Grabowiecka, Agnieszka,Bialas, Arkadiusz,Kosikowska, Paulina,Kafarski, Pawel
scheme or table, p. 1937 - 1945 (2012/10/18)
Small unextended molecules based on the diamidophosphate structure with a covalent carbon-to-phosphorus bond to improve hydrolytic stability were developed as a novel group of inhibitors to control microbial urea decomposition. Applying a structure-based
N-ALKYL-AMINOMETHYL-P-ETHYL- AND T-BUTYL-PHOSPHINIC ACID
Tyka, Roman,Haegele, Gerhard,Peters, Juergen
, p. 425 - 432 (2007/10/02)
Convenient one-batch-synthetic routes leading to the title compounds are described using easily accessible educts like N-alkyl-formamides, paraformaldehyde and alkyl- or aryldichlorophosphines.
N-ALKYL-N-PHOSPHONOMETHYLENE-AMINOMETHYL PHOSPHINIC ACIDS
Tyka, Roman,Haegele, Gerhard,Peters, Juergen
, p. 31 - 38 (2007/10/02)
The new compounds, R-N(CH2PO3H2)CH2P(R')O2H 3 (R=Me, Et, nPr, nBu, PhCH2; R'=Me, Et, Ph) are synthesized using a combination of previously reported and the MOEDRITZER reaction sequences.
