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A Photolabile Carboxyl Protecting Group for Solid Phase Peptide Synthesis

A new kind of photolabile protecting group (PLPG) for carboxyl moieties was designed and synthesized as the linker between resin and peptide. This group can be used for the protection of amino acid carboxyl groups. The peptide was synthesized on Nph (2‐hydroxy‐3‐(2‐nitrophenyl)‐heptanoic acid)‐deriv...

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Detalles Bibliográficos
Autores principales: Yang, Hongpeng, Peng, Tao, Wen, Xiaoxue, Chen, Tingting, Sun, Yunbo, Liu, Shuchen, Wang, Gang, Zhang, Shouguo, Wang, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080293/
https://www.ncbi.nlm.nih.gov/pubmed/33908701
http://dx.doi.org/10.1002/open.202000324
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author Yang, Hongpeng
Peng, Tao
Wen, Xiaoxue
Chen, Tingting
Sun, Yunbo
Liu, Shuchen
Wang, Gang
Zhang, Shouguo
Wang, Lin
author_facet Yang, Hongpeng
Peng, Tao
Wen, Xiaoxue
Chen, Tingting
Sun, Yunbo
Liu, Shuchen
Wang, Gang
Zhang, Shouguo
Wang, Lin
author_sort Yang, Hongpeng
collection PubMed
description A new kind of photolabile protecting group (PLPG) for carboxyl moieties was designed and synthesized as the linker between resin and peptide. This group can be used for the protection of amino acid carboxyl groups. The peptide was synthesized on Nph (2‐hydroxy‐3‐(2‐nitrophenyl)‐heptanoic acid)‐derivatized resins and could be cleaved under UV exposure, thus avoiding the necessity for harsh acid‐mediated resin cleavage. The PLPG has been successfully used for solid‐phase synthesis of peptides.
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spelling pubmed-80802932021-05-05 A Photolabile Carboxyl Protecting Group for Solid Phase Peptide Synthesis Yang, Hongpeng Peng, Tao Wen, Xiaoxue Chen, Tingting Sun, Yunbo Liu, Shuchen Wang, Gang Zhang, Shouguo Wang, Lin ChemistryOpen Full Papers A new kind of photolabile protecting group (PLPG) for carboxyl moieties was designed and synthesized as the linker between resin and peptide. This group can be used for the protection of amino acid carboxyl groups. The peptide was synthesized on Nph (2‐hydroxy‐3‐(2‐nitrophenyl)‐heptanoic acid)‐derivatized resins and could be cleaved under UV exposure, thus avoiding the necessity for harsh acid‐mediated resin cleavage. The PLPG has been successfully used for solid‐phase synthesis of peptides. John Wiley and Sons Inc. 2021-04-28 /pmc/articles/PMC8080293/ /pubmed/33908701 http://dx.doi.org/10.1002/open.202000324 Text en © 2021 The Authors. Published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full Papers
Yang, Hongpeng
Peng, Tao
Wen, Xiaoxue
Chen, Tingting
Sun, Yunbo
Liu, Shuchen
Wang, Gang
Zhang, Shouguo
Wang, Lin
A Photolabile Carboxyl Protecting Group for Solid Phase Peptide Synthesis
title A Photolabile Carboxyl Protecting Group for Solid Phase Peptide Synthesis
title_full A Photolabile Carboxyl Protecting Group for Solid Phase Peptide Synthesis
title_fullStr A Photolabile Carboxyl Protecting Group for Solid Phase Peptide Synthesis
title_full_unstemmed A Photolabile Carboxyl Protecting Group for Solid Phase Peptide Synthesis
title_short A Photolabile Carboxyl Protecting Group for Solid Phase Peptide Synthesis
title_sort photolabile carboxyl protecting group for solid phase peptide synthesis
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080293/
https://www.ncbi.nlm.nih.gov/pubmed/33908701
http://dx.doi.org/10.1002/open.202000324
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