Loading…
Radical‐Based Synthesis and Modification of Amino Acids
Amino acids (AAs) are key structural motifs with widespread applications in organic synthesis, biochemistry, and material sciences. Recently, with the development of milder and more versatile radical‐based procedures, the use of strategies relying on radical chemistry for the synthesis and modificat...
Saved in:
Published in: | Angewandte Chemie International Edition 2021-01, Vol.60 (3), p.1098-1115 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c5717-5a15f874adec82aaa78d54df15ee9e8edafd80a095142e2887c93a4223439c7e3 |
---|---|
cites | cdi_FETCH-LOGICAL-c5717-5a15f874adec82aaa78d54df15ee9e8edafd80a095142e2887c93a4223439c7e3 |
container_end_page | 1115 |
container_issue | 3 |
container_start_page | 1098 |
container_title | Angewandte Chemie International Edition |
container_volume | 60 |
creator | Aguilar Troyano, Francisco José Merkens, Kay Anwar, Khadijah Gómez‐Suárez, Adrián |
description | Amino acids (AAs) are key structural motifs with widespread applications in organic synthesis, biochemistry, and material sciences. Recently, with the development of milder and more versatile radical‐based procedures, the use of strategies relying on radical chemistry for the synthesis and modification of AAs has gained increased attention, as they allow rapid access to libraries of novel unnatural AAs containing a wide range of structural motifs. In this Minireview, we provide a broad overview of the advancements made in this field during the last decade, focusing on methods for the de novo synthesis of α‐, β‐, and γ‐AAs, as well as for the selective derivatisation of canonical and non‐canonical α‐AAs.
This Minireview provides a broad overview of the advancements made in the synthesis and modification of amino acid derivatives using radical chemistry during the last decade. The overview is divided in two sections: methods for the de novo synthesis of α‐, β‐, and γ‐amino acids, and methods for the selective derivatisation of canonical and non‐canonical α‐amino acids. |
doi_str_mv | 10.1002/anie.202010157 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7820943</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2476859060</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5717-5a15f874adec82aaa78d54df15ee9e8edafd80a095142e2887c93a4223439c7e3</originalsourceid><addsrcrecordid>eNqFkc1OWzEQha2qqNC02y7Rldh0c4N_Y3uDFCLaIkErFbq2pvbcYnRjw3XSKrs-Qp-RJ6mjQApsupqR5pujOXMIecfomFHKDyFFHHPKKaNM6RdkjynOWqG1eFl7KUSrjWK75HUp15U3hk5ekV3BjWRS0z1iv0KIHvq733-OoWBoLlZpcYUllgZSaM5ziF2dL2JOTe6a6Tym3Ex9DOUN2emgL_j2vo7Itw8nl7NP7dmXj6ez6VnrlWa6VcBUZ7SEgN5wANAmKBk6phAtGgzQBUOBWsUkx3qg9laA5FxIYb1GMSJHG92b5fc5Bo9pMUDvboY4h2HlMkT3dJLilfuRfzptOLX1AyPy_l5gyLdLLAs3j8Vj30PCvCyOS6ElldzSih48Q6_zckjVXqX0xChLJ2tqvKH8kEsZsNsew6hbp-LWqbhtKnVh_7GFLf4QQwXsBvgVe1z9R85NP5-e_BP_C0EMmWE</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2476859060</pqid></control><display><type>article</type><title>Radical‐Based Synthesis and Modification of Amino Acids</title><source>Wiley</source><creator>Aguilar Troyano, Francisco José ; Merkens, Kay ; Anwar, Khadijah ; Gómez‐Suárez, Adrián</creator><creatorcontrib>Aguilar Troyano, Francisco José ; Merkens, Kay ; Anwar, Khadijah ; Gómez‐Suárez, Adrián</creatorcontrib><description>Amino acids (AAs) are key structural motifs with widespread applications in organic synthesis, biochemistry, and material sciences. Recently, with the development of milder and more versatile radical‐based procedures, the use of strategies relying on radical chemistry for the synthesis and modification of AAs has gained increased attention, as they allow rapid access to libraries of novel unnatural AAs containing a wide range of structural motifs. In this Minireview, we provide a broad overview of the advancements made in this field during the last decade, focusing on methods for the de novo synthesis of α‐, β‐, and γ‐AAs, as well as for the selective derivatisation of canonical and non‐canonical α‐AAs.
This Minireview provides a broad overview of the advancements made in the synthesis and modification of amino acid derivatives using radical chemistry during the last decade. The overview is divided in two sections: methods for the de novo synthesis of α‐, β‐, and γ‐amino acids, and methods for the selective derivatisation of canonical and non‐canonical α‐amino acids.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>ISSN: 1521-3773</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.202010157</identifier><identifier>PMID: 32841470</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Amino acids ; Amino Acids - chemistry ; Chemical synthesis ; Humans ; Minireview ; Minireviews ; peptides ; Peptides - chemistry ; photochemistry ; Photochemistry - methods ; radical reactions ; Reviews ; synthetic methods</subject><ispartof>Angewandte Chemie International Edition, 2021-01, Vol.60 (3), p.1098-1115</ispartof><rights>2020 The Authors. Published by Wiley-VCH GmbH</rights><rights>2020 The Authors. Published by Wiley-VCH GmbH.</rights><rights>2020. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5717-5a15f874adec82aaa78d54df15ee9e8edafd80a095142e2887c93a4223439c7e3</citedby><cites>FETCH-LOGICAL-c5717-5a15f874adec82aaa78d54df15ee9e8edafd80a095142e2887c93a4223439c7e3</cites><orcidid>0000-0003-0753-2117 ; 0000-0001-5274-7219 ; 0000-0002-2799-0679 ; 0000-0003-4822-6554</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32841470$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aguilar Troyano, Francisco José</creatorcontrib><creatorcontrib>Merkens, Kay</creatorcontrib><creatorcontrib>Anwar, Khadijah</creatorcontrib><creatorcontrib>Gómez‐Suárez, Adrián</creatorcontrib><title>Radical‐Based Synthesis and Modification of Amino Acids</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>Amino acids (AAs) are key structural motifs with widespread applications in organic synthesis, biochemistry, and material sciences. Recently, with the development of milder and more versatile radical‐based procedures, the use of strategies relying on radical chemistry for the synthesis and modification of AAs has gained increased attention, as they allow rapid access to libraries of novel unnatural AAs containing a wide range of structural motifs. In this Minireview, we provide a broad overview of the advancements made in this field during the last decade, focusing on methods for the de novo synthesis of α‐, β‐, and γ‐AAs, as well as for the selective derivatisation of canonical and non‐canonical α‐AAs.
This Minireview provides a broad overview of the advancements made in the synthesis and modification of amino acid derivatives using radical chemistry during the last decade. The overview is divided in two sections: methods for the de novo synthesis of α‐, β‐, and γ‐amino acids, and methods for the selective derivatisation of canonical and non‐canonical α‐amino acids.</description><subject>Amino acids</subject><subject>Amino Acids - chemistry</subject><subject>Chemical synthesis</subject><subject>Humans</subject><subject>Minireview</subject><subject>Minireviews</subject><subject>peptides</subject><subject>Peptides - chemistry</subject><subject>photochemistry</subject><subject>Photochemistry - methods</subject><subject>radical reactions</subject><subject>Reviews</subject><subject>synthetic methods</subject><issn>1433-7851</issn><issn>1521-3773</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkc1OWzEQha2qqNC02y7Rldh0c4N_Y3uDFCLaIkErFbq2pvbcYnRjw3XSKrs-Qp-RJ6mjQApsupqR5pujOXMIecfomFHKDyFFHHPKKaNM6RdkjynOWqG1eFl7KUSrjWK75HUp15U3hk5ekV3BjWRS0z1iv0KIHvq733-OoWBoLlZpcYUllgZSaM5ziF2dL2JOTe6a6Tym3Ex9DOUN2emgL_j2vo7Itw8nl7NP7dmXj6ez6VnrlWa6VcBUZ7SEgN5wANAmKBk6phAtGgzQBUOBWsUkx3qg9laA5FxIYb1GMSJHG92b5fc5Bo9pMUDvboY4h2HlMkT3dJLilfuRfzptOLX1AyPy_l5gyLdLLAs3j8Vj30PCvCyOS6ElldzSih48Q6_zckjVXqX0xChLJ2tqvKH8kEsZsNsew6hbp-LWqbhtKnVh_7GFLf4QQwXsBvgVe1z9R85NP5-e_BP_C0EMmWE</recordid><startdate>20210118</startdate><enddate>20210118</enddate><creator>Aguilar Troyano, Francisco José</creator><creator>Merkens, Kay</creator><creator>Anwar, Khadijah</creator><creator>Gómez‐Suárez, Adrián</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0753-2117</orcidid><orcidid>https://orcid.org/0000-0001-5274-7219</orcidid><orcidid>https://orcid.org/0000-0002-2799-0679</orcidid><orcidid>https://orcid.org/0000-0003-4822-6554</orcidid></search><sort><creationdate>20210118</creationdate><title>Radical‐Based Synthesis and Modification of Amino Acids</title><author>Aguilar Troyano, Francisco José ; Merkens, Kay ; Anwar, Khadijah ; Gómez‐Suárez, Adrián</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5717-5a15f874adec82aaa78d54df15ee9e8edafd80a095142e2887c93a4223439c7e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Amino acids</topic><topic>Amino Acids - chemistry</topic><topic>Chemical synthesis</topic><topic>Humans</topic><topic>Minireview</topic><topic>Minireviews</topic><topic>peptides</topic><topic>Peptides - chemistry</topic><topic>photochemistry</topic><topic>Photochemistry - methods</topic><topic>radical reactions</topic><topic>Reviews</topic><topic>synthetic methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aguilar Troyano, Francisco José</creatorcontrib><creatorcontrib>Merkens, Kay</creatorcontrib><creatorcontrib>Anwar, Khadijah</creatorcontrib><creatorcontrib>Gómez‐Suárez, Adrián</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aguilar Troyano, Francisco José</au><au>Merkens, Kay</au><au>Anwar, Khadijah</au><au>Gómez‐Suárez, Adrián</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radical‐Based Synthesis and Modification of Amino Acids</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2021-01-18</date><risdate>2021</risdate><volume>60</volume><issue>3</issue><spage>1098</spage><epage>1115</epage><pages>1098-1115</pages><issn>1433-7851</issn><issn>1521-3773</issn><eissn>1521-3773</eissn><abstract>Amino acids (AAs) are key structural motifs with widespread applications in organic synthesis, biochemistry, and material sciences. Recently, with the development of milder and more versatile radical‐based procedures, the use of strategies relying on radical chemistry for the synthesis and modification of AAs has gained increased attention, as they allow rapid access to libraries of novel unnatural AAs containing a wide range of structural motifs. In this Minireview, we provide a broad overview of the advancements made in this field during the last decade, focusing on methods for the de novo synthesis of α‐, β‐, and γ‐AAs, as well as for the selective derivatisation of canonical and non‐canonical α‐AAs.
This Minireview provides a broad overview of the advancements made in the synthesis and modification of amino acid derivatives using radical chemistry during the last decade. The overview is divided in two sections: methods for the de novo synthesis of α‐, β‐, and γ‐amino acids, and methods for the selective derivatisation of canonical and non‐canonical α‐amino acids.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32841470</pmid><doi>10.1002/anie.202010157</doi><tpages>18</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0003-0753-2117</orcidid><orcidid>https://orcid.org/0000-0001-5274-7219</orcidid><orcidid>https://orcid.org/0000-0002-2799-0679</orcidid><orcidid>https://orcid.org/0000-0003-4822-6554</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1433-7851 |
ispartof | Angewandte Chemie International Edition, 2021-01, Vol.60 (3), p.1098-1115 |
issn | 1433-7851 1521-3773 1521-3773 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7820943 |
source | Wiley |
subjects | Amino acids Amino Acids - chemistry Chemical synthesis Humans Minireview Minireviews peptides Peptides - chemistry photochemistry Photochemistry - methods radical reactions Reviews synthetic methods |
title | Radical‐Based Synthesis and Modification of Amino Acids |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T09%3A48%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Radical%E2%80%90Based%20Synthesis%20and%20Modification%20of%20Amino%20Acids&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Aguilar%20Troyano,%20Francisco%20Jos%C3%A9&rft.date=2021-01-18&rft.volume=60&rft.issue=3&rft.spage=1098&rft.epage=1115&rft.pages=1098-1115&rft.issn=1433-7851&rft.eissn=1521-3773&rft_id=info:doi/10.1002/anie.202010157&rft_dat=%3Cproquest_pubme%3E2476859060%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5717-5a15f874adec82aaa78d54df15ee9e8edafd80a095142e2887c93a4223439c7e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2476859060&rft_id=info:pmid/32841470&rfr_iscdi=true |