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Innentitelbild: Recyclable Ligands for the Non-Enzymatic Dynamic Kinetic Resolution of Challenging α-Amino Acids (Angew. Chem. 44/2015).
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- Angewandte Chemie, 2015, v. 127, n. 44, p. 13018, doi. 10.1002/ange.201508520
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Recyclable Ligands for the Non-Enzymatic Dynamic Kinetic Resolution of Challenging α-Amino Acids.
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- Angewandte Chemie, 2015, v. 127, n. 44, p. 13110, doi. 10.1002/ange.201507273
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- Publication type:
- Article
Chemical Dynamic Kinetic Resolution and S/ R Interconversion of Unprotected α-Amino Acids.
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- Angewandte Chemie, 2014, v. 126, n. 45, p. 12410, doi. 10.1002/ange.201407944
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Convenient Asymmetric Synthesis of Fmoc-(S)-6,6,6-Trifluoro-Norleucine.
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- Symmetry (20738994), 2019, v. 11, n. 4, p. 578, doi. 10.3390/sym11040578
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New pharmaceuticals approved by FDA in 2020: Small‐molecule drugs derived from amino acids and related compounds.
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- Chirality, 2022, v. 34, n. 1, p. 86, doi. 10.1002/chir.23376
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Comparative study of different chiral ligands for dynamic kinetic resolution of amino acids.
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- Chirality, 2021, v. 33, n. 10, p. 685, doi. 10.1002/chir.23350
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Asymmetric synthesis of (S)‐3‐methyleneglutamic acid and its N‐Fmoc derivative via Michael addition–elimination reaction of chiral glycine Ni (II) complex with enol tosylates.
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- Chirality, 2021, v. 33, n. 3, p. 115, doi. 10.1002/chir.23291
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Asymmetric synthesis of (S)‐α‐(octyl)glycine via alkylation of Ni(II) complex of chiral glycine Schiff base.
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- Chirality, 2020, v. 32, n. 12, p. 1354, doi. 10.1002/chir.23281
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Michael addition reactions of chiral glycine Schiff base Ni (II)‐complex with 1‐(1‐phenylsulfonyl)benzene.
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- Chirality, 2020, v. 32, n. 6, p. 885, doi. 10.1002/chir.23203
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Asymmetric Synthesis of Tailor-Made Amino Acids Using Chiral Ni(II) Complexes of Schiff Bases. An Update of the Recent Literature.
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- Molecules, 2020, v. 25, n. 12, p. 2739, doi. 10.3390/molecules25122739
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Kitamura Electrophilic Fluorination Using HF as a Source of Fluorine.
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- Molecules, 2020, v. 25, n. 9, p. 2116, doi. 10.3390/molecules25092116
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- Article
Preparative Method for Asymmetric Synthesis of (S)-2-Amino-4,4,4-trifluorobutanoic Acid.
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- Molecules, 2019, v. 24, n. 24, p. 4521, doi. 10.3390/molecules24244521
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Optical Resolution of Rimantadine.
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- Molecules, 2019, v. 24, n. 9, p. 1828, doi. 10.3390/molecules24091828
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- Article
Asymmetric Synthesis of 4,4-(Difluoro)glutamic Acid via Chiral Ni(II)-Complexes of Dehydroalanine Schiff Bases. Effect of the Chiral Ligands Structure on the Stereochemical Outcome.
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- ChemistryOpen, 2020, v. 9, n. 1, p. 93, doi. 10.1002/open.201900343
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Large‐Scale Asymmetric Synthesis of Fmoc‐(S)‐2‐Amino‐6,6,6‐Trifluorohexanoic Acid.
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- ChemistryOpen, 2019, v. 8, n. 6, p. 701, doi. 10.1002/open.201900131
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- Article
Asymmetric Synthesis of N-Fmoc-(S)-7-aza-tryptophan via Alkylation of Chiral Nucleophilic Glycine Equivalent.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 21, p. 2962, doi. 10.1002/ejoc.202100485
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Operationally Convenient and Scalable Asymmetric Synthesis of (2S)- and (2R)-α-(Methyl)cysteine Derivatives through Alkylation of Chiral Alanine Schiff Base Ni<sup>II</sup> Complexes.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 14, p. 1931, doi. 10.1002/ejoc.201700018
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Asymmetric Synthesis of Aromatic and Heteroaromatic α-Amino Acids Using a Recyclable Axially Chiral Ligand.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 10, p. 1915, doi. 10.1002/ejoc.201600248
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Asymmetric Synthesis of Aromatic and Heteroaromatic α-Amino Acids Using a Recyclable Axially Chiral Ligand.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 5, p. 999, doi. 10.1002/ejoc.201501442
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- Article
Effect of substituents on the configurational stability of the stereogenic nitrogen in metal(II) complexes of α‐amino acid Schiff bases.
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- Chirality, 2019, v. 31, n. 5, p. 401, doi. 10.1002/chir.23066
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Chromatographic approach to study the configurational stability of Ni(II) complexes of amino‐acid Schiff bases possessing stereogenic nitrogen.
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- Chirality, 2019, v. 31, n. 4, p. 328, doi. 10.1002/chir.23059
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Axially chiral Ni(II) complexes of α‐amino acids: Separation of enantiomers and kinetics of racemization.
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- Chirality, 2018, v. 30, n. 4, p. 498, doi. 10.1002/chir.22815
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Inside Cover: Recyclable Ligands for the Non-Enzymatic Dynamic Kinetic Resolution of Challenging α-Amino Acids (Angew. Chem. Int. Ed. 44/2015).
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- Angewandte Chemie International Edition, 2015, v. 54, n. 44, p. 12826, doi. 10.1002/anie.201508520
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- Publication type:
- Article
Recyclable Ligands for the Non-Enzymatic Dynamic Kinetic Resolution of Challenging α-Amino Acids.
- Published in:
- Angewandte Chemie International Edition, 2015, v. 54, n. 44, p. 12918, doi. 10.1002/anie.201507273
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- Publication type:
- Article
Chemical Dynamic Kinetic Resolution and S/ R Interconversion of Unprotected α-Amino Acids.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 45, p. 12214, doi. 10.1002/anie.201407944
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- Article
Which Stereoinductor Is Better for Asymmetric Functionalization of α‐Amino Acids in a Nickel(II) Coordination Environment? Experimental and DFT Considerations.
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- Chemistry - A European Journal, 2020, v. 26, n. 31, p. 7074, doi. 10.1002/chem.201905708
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- Article
Synthesis of Ahod Moiety of Ralstonin A Using Amino Acid Schiff Base Ni(II)‐Complex Chemistry.
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- Helvetica Chimica Acta, 2020, v. 103, n. 7, p. 1, doi. 10.1002/hlca.202000077
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Eclipta thermalis, a previously common weed, threatened by the expansion of the exotic congener E. alba in Japanese rice paddies.
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- Ecological Research, 2024, v. 39, n. 3, p. 303, doi. 10.1111/1440-1703.12446
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Temporal variations in the linkages between plants and flower visitors and the pollination success of Primula modesta along the snowmelt gradient.
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- Nordic Journal of Botany, 2020, v. 38, n. 5, p. 1, doi. 10.1111/njb.02632
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Tailor-made amino acid-derived pharmaceuticals approved by the FDA in 2019.
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- Amino Acids, 2020, v. 52, n. 9, p. 1227, doi. 10.1007/s00726-020-02887-4
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Asymmetric synthesis of (2S,3S)-3-Me-glutamine and (R)-allo-threonine derivatives proper for solid-phase peptide coupling.
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- Amino Acids, 2019, v. 51, n. 3, p. 419, doi. 10.1007/s00726-018-2677-5
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Recent approaches for asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes.
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- Amino Acids, 2017, v. 49, n. 9, p. 1487, doi. 10.1007/s00726-017-2458-6
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Advanced asymmetric synthesis of (1 R,2 S)-1-amino-2-vinylcyclopropanecarboxylic acid by alkylation/cyclization of newly designed axially chiral Ni(II) complex of glycine Schiff base.
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- Amino Acids, 2016, v. 48, n. 4, p. 973, doi. 10.1007/s00726-015-2138-3
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Inexpensive chemical method for preparation of enantiomerically pure phenylalanine.
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- Amino Acids, 2014, v. 46, n. 4, p. 945, doi. 10.1007/s00726-013-1656-0
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Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 2: Aldol, Mannich addition reactions, deracemization and ( S) to ( R) interconversion of α-amino acids.
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- Amino Acids, 2013, v. 45, n. 5, p. 1017, doi. 10.1007/s00726-013-1580-3
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Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases; Part 1: alkyl halide alkylations.
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- Amino Acids, 2013, v. 45, n. 4, p. 691, doi. 10.1007/s00726-013-1539-4
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- Article