Strategy for synthesizing <i>O</i>-protected (<i>S</i>)-α-substituted serine analogs <i>via</i> sequential Ni(<scp>ii</scp>)-complex-mediated cross-coupling and cycloaddition reactions

A strategy for the synthesis of homochiral O -protected α-substituted ( S )-serine analogs by a sequence of reactions in the coordination sphere of a square-planar Ni( ii ) Schiff base complex of dehydroalanine and ( S )-BPB was developed.

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Publication Details

Journal
New Journal of Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5nj00764j
Citations
3
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
2.42

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article

Strategy for synthesizing O-protected (S)-α-substituted serine analogs via sequential Ni(ii)-complex-mediated cross-coupling and cycloaddition reactions

Peter Langer, Andrei V. Malkov, Anna F. Mkrtchyan, Ashot S. Saghyan et al.
3 citations
New Journal of Chemistry
Chemical Synthesis and Analysis
2.42
article

Strategy for synthesizing O-protected (S)-α-substituted serine analogs via sequential Ni(ii)-complex-mediated cross-coupling and cycloaddition reactions

Peter Langer, Andrei V. Malkov, Anna F. Mkrtchyan, Ashot S. Saghyan, Anna S. Tovmasyan, Avetis Tsaturyan
article en
3 citations

Abstract

A strategy for the synthesis of homochiral O -protected α-substituted ( S )-serine analogs by a sequence of reactions in the coordination sphere of a square-planar Ni( ii ) Schiff base complex of dehydroalanine and ( S )-BPB was developed.

New Journal of ChemistryVol. 49(27)
Loughborough University (GB), Yerevan State University (AM), Institute of Chemical Physics NAS RA (AM), University of Rostock (DE)
International Science and Technology Center
Openalex Percentile: Top 11%
Chemical Synthesis and Analysis
2.42
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