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Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions

Copper(II)-peptides are widely used as industrial catalysts such as in the aerobic oxidation of organic molecules, formation of new C–H bonds and in the azide–alkyne cycloaddition reaction. The length of peptides and the effect of adding copper metal into peptides were questioned in their field of a...

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Huvudupphovsmän: Begum, Sharifa Zaithun, Abdul Malek, Emilia, Mohamed Tahir, Mohamed Ibrahim, Crouse, Karen Anne, Abdul Rahman, Mohd Basyaruddin
Materialtyp: Artikel
Språk:English
Publicerad: Royal Society of Chemistry 2018
Länkar:http://psasir.upm.edu.my/id/eprint/74512/1/Histidine-based.pdf
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spelling oai:psasir.upm.edu.my:74512 http://psasir.upm.edu.my/id/eprint/74512/ Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions Begum, Sharifa Zaithun Abdul Malek, Emilia Mohamed Tahir, Mohamed Ibrahim Crouse, Karen Anne Abdul Rahman, Mohd Basyaruddin Copper(II)-peptides are widely used as industrial catalysts such as in the aerobic oxidation of organic molecules, formation of new C–H bonds and in the azide–alkyne cycloaddition reaction. The length of peptides and the effect of adding copper metal into peptides were questioned in their field of applications. Five novel histidine-based tetrapeptides with the sequences HAAD (P1), HAFD (P2), HAVD (P3), AGHD (P4) and PGHD (P5) were synthesized using the solid phase peptide scheme and analysed with high performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS) with percentage purities as high as 99.5%. All the peptides were positively charged (+1) and the molecular weight calculated from m/z values of MS results coincided with the theoretical molecular weight of the peptides. Copper(II)-peptides derived from these peptides and copper(II) acetate monohydrate (CuP1–CuP5) in a 1 : 2 ratio was synthesised, purified and characterised by ultraviolet-visible spectroscopy (UV-Vis), ultraviolet-fluorescence spectroscopy (fluorescence) and fourier transform infrared spectroscopy (FTIR), circular dichroism spectroscopy (CD) and optical rotation polarimetry. It provided the necessary information on the secondary structure and the successful binding of copper(II) to the specific amino acids, hence leading to the putative geometry of copper(II)-peptides and the difference in the chirality of amino acids, peptides and copper(II)-peptides. The catalytic activities of the synthesised complexes were evaluated. CuP1 & CuP3 catalysed both the asymmetric aldol reactions with high enantioselectivity of p-nitrobenzaldehyde with cyclohexanone (% ee = 87.3 & 80.3, respectively) and of p-anisaldehyde with cyclohexanone (% ee = 95.5 & 90.9, respectively). Royal Society of Chemistry 2018 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/74512/1/Histidine-based.pdf Begum, Sharifa Zaithun and Abdul Malek, Emilia and Mohamed Tahir, Mohamed Ibrahim and Crouse, Karen Anne and Abdul Rahman, Mohd Basyaruddin (2018) Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions. RSC Advances, 8. 34004 - 34011. ISSN 2046-2069 10.1039/c8ra06814c
institution UPM IR
collection UPM IR
language English
description Copper(II)-peptides are widely used as industrial catalysts such as in the aerobic oxidation of organic molecules, formation of new C–H bonds and in the azide–alkyne cycloaddition reaction. The length of peptides and the effect of adding copper metal into peptides were questioned in their field of applications. Five novel histidine-based tetrapeptides with the sequences HAAD (P1), HAFD (P2), HAVD (P3), AGHD (P4) and PGHD (P5) were synthesized using the solid phase peptide scheme and analysed with high performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS) with percentage purities as high as 99.5%. All the peptides were positively charged (+1) and the molecular weight calculated from m/z values of MS results coincided with the theoretical molecular weight of the peptides. Copper(II)-peptides derived from these peptides and copper(II) acetate monohydrate (CuP1–CuP5) in a 1 : 2 ratio was synthesised, purified and characterised by ultraviolet-visible spectroscopy (UV-Vis), ultraviolet-fluorescence spectroscopy (fluorescence) and fourier transform infrared spectroscopy (FTIR), circular dichroism spectroscopy (CD) and optical rotation polarimetry. It provided the necessary information on the secondary structure and the successful binding of copper(II) to the specific amino acids, hence leading to the putative geometry of copper(II)-peptides and the difference in the chirality of amino acids, peptides and copper(II)-peptides. The catalytic activities of the synthesised complexes were evaluated. CuP1 & CuP3 catalysed both the asymmetric aldol reactions with high enantioselectivity of p-nitrobenzaldehyde with cyclohexanone (% ee = 87.3 & 80.3, respectively) and of p-anisaldehyde with cyclohexanone (% ee = 95.5 & 90.9, respectively).
format Article
author Begum, Sharifa Zaithun
Abdul Malek, Emilia
Mohamed Tahir, Mohamed Ibrahim
Crouse, Karen Anne
Abdul Rahman, Mohd Basyaruddin
spellingShingle Begum, Sharifa Zaithun
Abdul Malek, Emilia
Mohamed Tahir, Mohamed Ibrahim
Crouse, Karen Anne
Abdul Rahman, Mohd Basyaruddin
Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions
author_facet Begum, Sharifa Zaithun
Abdul Malek, Emilia
Mohamed Tahir, Mohamed Ibrahim
Crouse, Karen Anne
Abdul Rahman, Mohd Basyaruddin
author_sort Begum, Sharifa Zaithun
title Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions
title_short Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions
title_full Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions
title_fullStr Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions
title_full_unstemmed Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions
title_sort histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions
publisher Royal Society of Chemistry
publishDate 2018
url http://psasir.upm.edu.my/id/eprint/74512/1/Histidine-based.pdf
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score 13.4562235

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