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Aminofosfonato (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Aminofosfonato" in Spanish language version.

refsWebsite
Global rank Spanish rank
17doi.org
2nd place
2nd place
3nih.gov
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1organic-chemistry.org
low place
low place
1handle.net
102nd place
516th place
1google.com
163rd place
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doi.org

dx.doi.org

  • Pedro Merino; Eugenia Marqués-López; Raquel P. Herrera (2008). «Catalytic Enantioselective Hydrophosphonylation of Aldehydes and Imines». Advanced Synthesis & Catalysis 350: 1195-1208. doi:10.1002/adsc.200800131. 
  • Tušek-Božić, LJ (2013). «Aminophosphonate metal complexes of biomedical potential.». Current Medicinal Chemistry 20 (16): 2096-117. PMID 23432587. doi:10.2174/0929867311320160004. 
  • Orsini, F; Sello, G; Sisti, M (2010). «Aminophosphonic acids and derivatives. Synthesis and biological applications.». Current Medicinal Chemistry 17 (3): 264-89. PMID 20214568. doi:10.2174/092986710790149729. 
  • M. Horiguchi, M. Kandatsu (1959). «Isolation of 2 - aminoethane phosphonic acid from rumen protozoa.». Nature 184: 901. doi:10.1038/184901b0. 
  • H. Shimizu, Y. Kakimoto, T. Nakajima, A. Kanazawa & I. Sano (1965). «Isolation and Identification of 2-Aminoethyl-phosphonic Acid from Bovine Brain». Nature 207: 1197 - 1198. doi:10.1038/2071197a0. 
  • S. Sachdeva (2017). «Peptides as ‘Drugs’: The Journey so Far». Int J Pept Res Ther 23: 49–60. doi:10.1007/s10989-016-9534-8. 
  • Acena JL, Simon-Fuentes A, Fustero S. (2010). «Recent Developments in the Synthesis of Fluorinated β-Amino Acids». Current Organic Chemistry 14 (9): 928-949. doi:10.2174/138527210791111777. 
  • Cativiela C, Ordóñez M. (2009). «Recent progress on the stereoselective synthesis of cyclic quaternary α-amino acids». Tetrahedron: Asymmetry 20 (1): 1-63. doi:10.1016/j.tetasy.2009.01.002. 
  • Aceña JL, Sorochinsky AE, Soloshonok VA (2012). «Recent Advances in the Asymmetric Synthesis of α-(Trifluoromethyl)-Containing α-Amino Acids». Synthesis 44 (11): 1591-1602. doi:10.1055/s-0031-1289756. 
  • Choudhary A, Raines RT (2011). «An Evaluation of Peptide‐Bond Isosteres». ChemBioChem 12: 1801-1807. doi:10.1002/cbic.201100272. 
  • N. Azizi, M. R. Saidi (2003). «Synthesis of tertiary α-amino phosphonate by one-pot three-component coupling mediated by LPDE». Tetrahedron 59: 5329-5332. doi:10.1016/S0040-4020(03)00759-2. 
  • B. Kaboudin, K. Moradi (2005). «A simple and convenient procedure for the synthesis of 1-aminophosphonates from aromatic aldehydes». Tetrahedron Letters 46: 2989-2991. doi:10.1016/j.tetlet.2005.03.037. 
  • Ali, Tarik E.; Abdel-Kariem, Somaia M. (2015). «Methods for the synthesis of α-heterocyclic/heteroaryl-α-aminophosphonic acids and their esters». Arkivoc: Reviews and Accounts 2015 (6): 246-287. doi:10.3998/ark.5550190.p009.112. 
  • Foroogh Bahrami; Farhad Panahi; Ali Khalafinezhad (2016). «Synthesis of new α-aminophosphonate derivatives incorporating benzimidazole, theophylline and adenine nucleobases using L-cysteine functionalized magnetic nanoparticles (LCMNP) as magnetic reusable catalyst: evaluation of their anticancer properties». RSC Advances 6 (9): 5915-5924. doi:10.1039/C5RA21419J. hdl:10261/114023. 
  • Mucha, Artur; Kafarski, Paweł; Berlicki, Łukasz (2011). «Remarkable Potential of the α-Aminophosphonate/Phosphinate Structural Motif in Medicinal Chemistry». Journal of Medicinal Chemistry 54 (17): 5955-5980. PMID 21780776. doi:10.1021/jm200587f. 
  • Hirschmann, R.; Smith, A.B.; Taylor, C.M.; Benkovic, P.A.; Taylor, S.D.; Yager, K.M.; Sprengler, P.A.; Benkovic, S.J. (1994). «Peptide synthesis catalyzed by an antibody containing a binding site for variable amino acids». Science 265: 234-237. doi:10.1126/science.8023141. 
  • T. Kametani, K. Kigasawa, M. Hiiragi, K. Wakisaka, S. Haga, H. Sugi, K. Tanigawa, Y. Suzuki, K. Fukawa, O. Irino, O. Saita, and S. Yamabe (1981). «Studies on the Synthesis of Chemotherpeutics. Part XI. Synthesis and Antibacterial Activities of Phosphonopeptides». HetroCycles 16 (7): 1205-1242. doi:10.3987/R-1981-07-1205. 

google.com

handle.net

hdl.handle.net

  • Foroogh Bahrami; Farhad Panahi; Ali Khalafinezhad (2016). «Synthesis of new α-aminophosphonate derivatives incorporating benzimidazole, theophylline and adenine nucleobases using L-cysteine functionalized magnetic nanoparticles (LCMNP) as magnetic reusable catalyst: evaluation of their anticancer properties». RSC Advances 6 (9): 5915-5924. doi:10.1039/C5RA21419J. hdl:10261/114023. 

nih.gov

ncbi.nlm.nih.gov

  • Tušek-Božić, LJ (2013). «Aminophosphonate metal complexes of biomedical potential.». Current Medicinal Chemistry 20 (16): 2096-117. PMID 23432587. doi:10.2174/0929867311320160004. 
  • Orsini, F; Sello, G; Sisti, M (2010). «Aminophosphonic acids and derivatives. Synthesis and biological applications.». Current Medicinal Chemistry 17 (3): 264-89. PMID 20214568. doi:10.2174/092986710790149729. 
  • Mucha, Artur; Kafarski, Paweł; Berlicki, Łukasz (2011). «Remarkable Potential of the α-Aminophosphonate/Phosphinate Structural Motif in Medicinal Chemistry». Journal of Medicinal Chemistry 54 (17): 5955-5980. PMID 21780776. doi:10.1021/jm200587f. 

organic-chemistry.org