ArticleMolecules (Basel, Switzerland)2020
The Synthesis of α-Aminophosphonates via Enantioselective Organocatalytic Reaction of 1-(
Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- A new class of anticancer activity with computational studies for a novel bioactive aminophosphonates based on pyrazole moiety.Scientific reports · 2023Article
- The Last Decade of Optically Active α-Aminophosphonates.Molecules (Basel, Switzerland) · 2023Review
- Facile Conversion of α-Amino Acids into α-Amino Phosphonates by Decarboxylative Phosphorylation using Visible-Light Photocatalysis.Angewandte Chemie (International ed. in English) · 2022Article
- 1-Aminoalkylphosphonium Derivatives: Smart Synthetic Equivalents ofMolecules (Basel, Switzerland) · 2022Review
- Non-Kolbe electrolysis ofRSC advances · 2022Article
- Design, Synthesis, and Spectroscopic Studies of Some New α-Aminophosphonate Analogues Derived from 4-Hydroxybenzaldehyde with Special Reference to Anticancer Activity.Drug design, development and therapy · 2022Article
- Recommended Tests for the Self-Disproportionation of Enantiomers (SDE) to Ensure Accurate Reporting of the Stereochemical Outcome of Enantioselective Reactions.Molecules (Basel, Switzerland) · 2021Review
- Synthesis ofThe Journal of organic chemistry · 2021Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
α-Aminophosphonic acids are phosphorus analogues of α-amino acids. Compounds of this type find numerous applications in medicine and crop protection due to their unique biological activities. A crucial factor in these activities is the configuration of the stereoisomers. Only a few methods of stereoselective transformation of α-amino acids into their phosphorus analogues are known so far and all of them are based on asymmetric induction, thus involving the use of a chiral substrate. In contrast, we have focused our efforts on the development of an effective method for this type of transformation using a racemic mixture of starting
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Registered trials
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