ChemInform Abstract: AMINOPHOSPHONIC ACIDS. PART VIII. APPLICATION OF TRICHLOROACETONITRILE FOR PREPARATION OF α-AMINOPHOSPHONIC ACID MONOESTERS

1977 ◽  
Vol 8 (7) ◽  
pp. no-no
Author(s):  
C. WASIELEWSKI ◽  
M. HOFFMANN ◽  
E. WITKOWSKA ◽  
J. RACHON
2019 ◽  
Vol 17 (31) ◽  
pp. 7352-7359 ◽  
Author(s):  
Jakub Iwanejko ◽  
Anna Brol ◽  
Bartłomiej M. Szyja ◽  
Marek Daszkiewicz ◽  
Elżbieta Wojaczyńska ◽  
...  

Chiral tetrasubstituted aminophosphonic acid derivatives of hexahydroquinoxalin-2(1H)-one were synthesised via diastereoselective hydrophosphonylation of corresponding imines with tris(trimethylsilyl)phosphite as phosphorus nucleophile.


2001 ◽  
Vol 3 (4) ◽  
pp. 217-221 ◽  
Author(s):  
A. Paladini ◽  
C. Calcagni ◽  
T. Di. Palma ◽  
M. Satta ◽  
M. Speranza ◽  
...  

Clusters between first-group metal ions and chiralα-aminophosphonic acids have been readily generated by Pulsed Laser Ablation (PLA) and by Electrospray Ionization (ESI) and their fragmentation investigated by mass spectrometry. The complexes studied have the general formula[Me(I)Cl2]+, where Me(I) is H, Li, Na, or K, C is (R)-(—)-(1-aminoethyl) phosphonic acid(ER)and (S)-(+)-(1-aminoethyl) phosphonic acid(ES),(1R)-(+)-(1-amino-2-methylpropyl) phosphonic acid(PR)and (1S)-(—)-(1-amino-2-methylpropyl) phosphonic acid(PS),(1R)-(-)-(1-amino-hexyl) phosphonic acid (HR) and (1S)-(+)-(1-amino-hexyl) phosphonic acid (HS), o-phospho-L-serine (SS)ando-phospho-D-serine(SR), and L is a referenceα-aminophosphonic acid (E, P, H or S) of defined configuration. Collision induced dissociation (CID) of diastereomeric[Me(I)Cl2]+complexes leads to fragmentation patterns characterized by[Me(I)Cl]+/[Me(I)L2]+abundance ratios which depend upon the configuration of solute C. These different spectral features were correlated to the different stability of the diastereomeric[Me(I)CRL]+and[Me(I)CSL]+complexes in the gas phase.


Organics ◽  
2021 ◽  
Vol 2 (2) ◽  
pp. 72-83
Author(s):  
Oksana M. Shavrina ◽  
Lyudmyla V. Bezgubenko ◽  
Andrii V. Bezdudny ◽  
Petro P. Onys’ko ◽  
Yuliya V. Rassukana

A convenient synthetic approach to previously unknown NH-iminophosphonates bearing 2-, 3-, and 4-pyridyldifluoromethyl groups at the imine carbon atom was developed. The synthetic potential of these novel building blocks was demonstrated by their conversion into highly functionalized acyclic and heterocyclic aminophosphonates and phosphonic acids combining in their structure biorelevant aminophosphonic fragment, difluoromethyl group, and pyridyl, piperidyl, thiazolidin-4-one, or thiazidinan-4-one heterocyclic moieties in a single molecular platform.


1985 ◽  
Vol 68 (6) ◽  
pp. 1730-1747 ◽  
Author(s):  
Rolf Huber ◽  
Andreas Knierzinger ◽  
Jean-Pierre Obrecht ◽  
Andrea Vasella

ChemInform ◽  
2001 ◽  
Vol 32 (39) ◽  
pp. no-no
Author(s):  
Giancarlo Cravotto ◽  
Giovanni B. Giovenzana ◽  
Roberto Pagliarin ◽  
Giovanni Palmisano ◽  
Massimo Sisti

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