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Biocatalytic Production of Aldehydes: Exploring the Potential of Lathyrus cicera Amine Oxidase.

• Authors : Di Fabio E; Department of Biochemical Sciences 'Alessandro Rossi Fanelli', Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy.; Incocciati A

Subjects: Aldehydes/Aldehydes/Aldehydes/*chemical synthesis ; Amine Oxidase (Copper-Containing)/Amine Oxidase (Copper-Containing)/Amine Oxidase (Copper-Containing)/*chemistry ; Amines/Amines/Amines/*chemistry

• Source: Biomolecules [Biomolecules] 2021 Oct 18; Vol. 11 (10). Date of Electronic Publication: 2021 Oct 18.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101596414 Publication Model: Electronic Cited Medium: Internet ISSN: 2218-273X

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Acidic Shift of Optimum pH of Bovine Serum Amine Oxidase upon Immobilization onto Nanostructured Ferric Tannates.

• Authors : Rilievo, Graziano¹ (AUTHOR); Cecconello, Alessandro¹ (AUTHOR); Molinari, Simone² (AUTHOR)

Subjects: *AMINE oxidase; *TANNINS; *BOS

• Source: International Journal of Molecular Sciences. Oct2022, Vol. 23 Issue 20, p12172-N.PAG. 18p.

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Immobilization of Lathyrus cicera Amine Oxidase on Magnetic Microparticles for Biocatalytic Applications.

• Authors : Di Fabio, Elisa¹ (AUTHOR) ; Iazzetti, Antonia^2,3 (AUTHOR) ; Incocciati, Alessio¹ (AUTHOR)

Subjects: *AMINE oxidase; *IMMOBILIZED enzymes; *BIOCATALYSIS

• Source: International Journal of Molecular Sciences. Jun2022, Vol. 23 Issue 12, p6529-6529. 14p.

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HPLC-UV method for evaluation of inhibitors of plasma amine oxidase using derivatization of an aliphatic aldehyde product with TRIS.

• Authors : Mergemeier K; Institute of Pharmaceutical and Medicinal Chemistry, University of Münster, Corrensstrasse 48, 48149, Münster, Germany.; Lehr M

Subjects: Aldehydes/Aldehydes/Aldehydes/*pharmacology ; Amine Oxidase (Copper-Containing)/Amine Oxidase (Copper-Containing)/Amine Oxidase (Copper-Containing)/*blood ; Chromatography, High Pressure Liquid/Chromatography, High Pressure Liquid/Chromatography, High Pressure Liquid/*methods

• Source: Analytical and bioanalytical chemistry [Anal Bioanal Chem] 2016 Jul; Vol. 408 (17), pp. 4799-807. Date of Electronic Publication: 2016 Apr 29.Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 101134327 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Synthesis of Pluri-Functional Amine Hardeners from Bio-Based Aromatic Aldehydes for Epoxy Amine Thermosets.

• Authors : Mora AS; Institut Charles Gerhardt, UMR 5253-CNRS, Université de Montpellier, Ecole Nationale Supérieure de Chimie de Montpellier, 240 Avenue Emile Jeanbrau, 34296 Montpellier, France. .; Tayouo R

Subjects: Aldehydes/Aldehydes/Aldehydes/*chemistry ; Amines/Amines/Amines/*chemistry ; Epoxy Resins/Epoxy Resins/Epoxy Resins/*chemistry

• Source: Molecules (Basel, Switzerland) [Molecules] 2019 Sep 09; Vol. 24 (18). Date of Electronic Publication: 2019 Sep 09.Publisher: MDPI Country of Publication: Switzerland NLM ID: 100964009 Publication Model: Electronic Cited Medium: Internet ISSN: 1420-3049

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Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates.

• Authors : Kawanishi R; Department of Applied Chemistry and Life Science, Toyohashi University of Technology, 1-1 Hibarigaoka, Tempaku-cho, Toyohashi 441-8580, Japan.; Hattori S

Subjects: Aldehydes/Aldehydes/Aldehydes/*chemistry ; Carboxylic Acids/Carboxylic Acids/Carboxylic Acids/*chemistry ; Cinchona Alkaloids/Cinchona Alkaloids/Cinchona Alkaloids/*chemistry

• Source: Molecules (Basel, Switzerland) [Molecules] 2019 Jul 30; Vol. 24 (15). Date of Electronic Publication: 2019 Jul 30.Publisher: MDPI Country of Publication: Switzerland NLM ID: 100964009 Publication Model: Electronic Cited Medium: Internet ISSN: 1420-3049

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Advances in the Asymmetric Total Synthesis of Natural Products Using Chiral Secondary Amine Catalyzed Reactions of α,β-Unsaturated Aldehydes.

• Authors : Wang Z; School of Pharmaceutical Sciences, Tsinghua University, Beijing 100084, China. .; School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu 273165, China. .

Subjects: Aldehydes/Aldehydes/Aldehydes/*chemistry ; Amines/Amines/Amines/*chemistry ; Biological Products/Biological Products/Biological Products/*chemical synthesis

• Source: Molecules (Basel, Switzerland) [Molecules] 2019 Sep 19; Vol. 24 (18). Date of Electronic Publication: 2019 Sep 19.Publisher: MDPI Country of Publication: Switzerland NLM ID: 100964009 Publication Model: Electronic Cited Medium: Internet ISSN: 1420-3049

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The Asymmetric A³(Aldehyde⁻Alkyne⁻Amine) Coupling: Highly Enantioselective Access to Propargylamines.

• Authors : Mo JN; Zhang Dayu School of Chemistry, Dalian University of Technology, Dalian 116024, China. .; Su J

Subjects: Aldehydes/Aldehydes/Aldehydes/*chemistry ; Alkynes/Alkynes/Alkynes/*chemistry ; Amines/Amines/Amines/*chemistry

• Source: Molecules (Basel, Switzerland) [Molecules] 2019 Mar 28; Vol. 24 (7). Date of Electronic Publication: 2019 Mar 28.Publisher: MDPI Country of Publication: Switzerland NLM ID: 100964009 Publication Model: Electronic Cited Medium: Internet ISSN: 1420-3049

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Enantioselective Michael Addition of Aldehydes to Maleimides Organocatalyzed by a Chiral Primary Amine-Salicylamide.

• Authors : Torregrosa-Chinillach A; Departamento de Química Orgánica, Facultad de Ciencias, and Instituto de Síntesis Orgánica (ISO), Uni-versidad de Alicante, Apdo. 99, 03080 Alicante, Spain. .; Moragues A

Subjects: Aldehydes/Aldehydes/Aldehydes/*chemistry ; Maleimides/Maleimides/Maleimides/*chemistry ; Salicylamides/Salicylamides/Salicylamides/*chemistry

• Source: Molecules (Basel, Switzerland) [Molecules] 2018 Dec 12; Vol. 23 (12). Date of Electronic Publication: 2018 Dec 12.Publisher: MDPI Country of Publication: Switzerland NLM ID: 100964009 Publication Model: Electronic Cited Medium: Internet ISSN: 1420-3049

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Chiral Primary Amine Catalysis for Asymmetric Mannich Reactions of Aldehydes with Ketimines: Stereoselectivity and Reactivity.

• Authors : Dai, Jun¹; Xiong, Dan¹; Yuan, Tengrui¹

• Source: Angewandte Chemie. Oct2017, Vol. 129 Issue 41, p12871-12875. 5p.

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