Exploiting photooxygenations mediated by porphyrinoid photocatalysts under continuous flow conditions
Photooxygenation reactions are a powerful synthetic tool to produce oxidized organic compounds; however, these reactions often exhibit experimental limitations including the production of complex mixtures that hinder desired product isolation and scale-up. Herein, we present a photocatalysed protoco...
Gespeichert in:
Veröffentlicht in: | RSC advances 2016-01, Vol.6 (16), p.12717-12725 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 12725 |
---|---|
container_issue | 16 |
container_start_page | 12717 |
container_title | RSC advances |
container_volume | 6 |
creator | de Oliveira, Kleber T Miller, L. Zane McQuade, D. Tyler |
description | Photooxygenation reactions are a powerful synthetic tool to produce oxidized organic compounds; however, these reactions often exhibit experimental limitations including the production of complex mixtures that hinder desired product isolation and scale-up. Herein, we present a photocatalysed protocol under continuous flow conditions using a simple home built photoreactor and porphyrinoids as photocatalysts. Reaction conditions, long-term experiments, and scope demonstrate a protocol that is cost-effective, safe, reproducible and robust, thus allowing the production of relevant substituted naphthoquinones with interest in natural product synthesis and biological activity.
Photooxygenations of naphthols under continuous flow conditions using porphyrinoids as photocatalysts are described. Reaction conditions, long-term experiments and scope were performed, thus allowing the production of substituted naphthoquinones. |
doi_str_mv | 10.1039/c6ra00285d |
format | Article |
fullrecord | <record><control><sourceid>proquest_rsc_p</sourceid><recordid>TN_cdi_rsc_primary_c6ra00285d</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1800481085</sourcerecordid><originalsourceid>FETCH-LOGICAL-c352t-1110fa66f533d599ebf2c15bf372b117f2f7ee795fe961c8783cdb75293858083</originalsourceid><addsrcrecordid>eNpNkF1LwzAUhoMoOOZuvBd6KUI1H0uaXo45P2AgiF6XNB9bpEtqkuL67-1WUc_NOS88vBweAC4RvEWQlHeSBQEh5lSdgAmGc5ZjyMrTf_c5mMX4AYdhFGGGJkCv9m3jbbJuk7Vbn7zf9xvtRLLexWynlRVJq6zus9aHdtsH67xVIypFEk0fU8w6p3TIpHdDT-e7mJnGfx2ysseiC3BmRBP17GdPwfvD6m35lK9fHp-Xi3UuCcUpRwhBIxgzlBBFy1LXBktEa0MKXCNUGGwKrYuSGl0yJHnBiVR1QXFJOOWQkym4Hnvb4D87HVO1s1HqphFOD29ViEM45whyOqA3IyqDjzFoU7XB7kToKwSrg85qyV4XR533A3w1wiHKX-5PN_kG97J0Pw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1800481085</pqid></control><display><type>article</type><title>Exploiting photooxygenations mediated by porphyrinoid photocatalysts under continuous flow conditions</title><source>Royal Society Of Chemistry Journals 2008-</source><creator>de Oliveira, Kleber T ; Miller, L. Zane ; McQuade, D. Tyler</creator><creatorcontrib>de Oliveira, Kleber T ; Miller, L. Zane ; McQuade, D. Tyler</creatorcontrib><description>Photooxygenation reactions are a powerful synthetic tool to produce oxidized organic compounds; however, these reactions often exhibit experimental limitations including the production of complex mixtures that hinder desired product isolation and scale-up. Herein, we present a photocatalysed protocol under continuous flow conditions using a simple home built photoreactor and porphyrinoids as photocatalysts. Reaction conditions, long-term experiments, and scope demonstrate a protocol that is cost-effective, safe, reproducible and robust, thus allowing the production of relevant substituted naphthoquinones with interest in natural product synthesis and biological activity.
Photooxygenations of naphthols under continuous flow conditions using porphyrinoids as photocatalysts are described. Reaction conditions, long-term experiments and scope were performed, thus allowing the production of substituted naphthoquinones.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/c6ra00285d</identifier><language>eng</language><subject>Biological ; Continuous flow ; Natural products ; Organic compounds ; Photocatalysis ; Photocatalysts ; Synthesis (chemistry)</subject><ispartof>RSC advances, 2016-01, Vol.6 (16), p.12717-12725</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-1110fa66f533d599ebf2c15bf372b117f2f7ee795fe961c8783cdb75293858083</citedby><cites>FETCH-LOGICAL-c352t-1110fa66f533d599ebf2c15bf372b117f2f7ee795fe961c8783cdb75293858083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>de Oliveira, Kleber T</creatorcontrib><creatorcontrib>Miller, L. Zane</creatorcontrib><creatorcontrib>McQuade, D. Tyler</creatorcontrib><title>Exploiting photooxygenations mediated by porphyrinoid photocatalysts under continuous flow conditions</title><title>RSC advances</title><description>Photooxygenation reactions are a powerful synthetic tool to produce oxidized organic compounds; however, these reactions often exhibit experimental limitations including the production of complex mixtures that hinder desired product isolation and scale-up. Herein, we present a photocatalysed protocol under continuous flow conditions using a simple home built photoreactor and porphyrinoids as photocatalysts. Reaction conditions, long-term experiments, and scope demonstrate a protocol that is cost-effective, safe, reproducible and robust, thus allowing the production of relevant substituted naphthoquinones with interest in natural product synthesis and biological activity.
Photooxygenations of naphthols under continuous flow conditions using porphyrinoids as photocatalysts are described. Reaction conditions, long-term experiments and scope were performed, thus allowing the production of substituted naphthoquinones.</description><subject>Biological</subject><subject>Continuous flow</subject><subject>Natural products</subject><subject>Organic compounds</subject><subject>Photocatalysis</subject><subject>Photocatalysts</subject><subject>Synthesis (chemistry)</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpNkF1LwzAUhoMoOOZuvBd6KUI1H0uaXo45P2AgiF6XNB9bpEtqkuL67-1WUc_NOS88vBweAC4RvEWQlHeSBQEh5lSdgAmGc5ZjyMrTf_c5mMX4AYdhFGGGJkCv9m3jbbJuk7Vbn7zf9xvtRLLexWynlRVJq6zus9aHdtsH67xVIypFEk0fU8w6p3TIpHdDT-e7mJnGfx2ysseiC3BmRBP17GdPwfvD6m35lK9fHp-Xi3UuCcUpRwhBIxgzlBBFy1LXBktEa0MKXCNUGGwKrYuSGl0yJHnBiVR1QXFJOOWQkym4Hnvb4D87HVO1s1HqphFOD29ViEM45whyOqA3IyqDjzFoU7XB7kToKwSrg85qyV4XR533A3w1wiHKX-5PN_kG97J0Pw</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>de Oliveira, Kleber T</creator><creator>Miller, L. Zane</creator><creator>McQuade, D. Tyler</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20160101</creationdate><title>Exploiting photooxygenations mediated by porphyrinoid photocatalysts under continuous flow conditions</title><author>de Oliveira, Kleber T ; Miller, L. Zane ; McQuade, D. Tyler</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-1110fa66f533d599ebf2c15bf372b117f2f7ee795fe961c8783cdb75293858083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Biological</topic><topic>Continuous flow</topic><topic>Natural products</topic><topic>Organic compounds</topic><topic>Photocatalysis</topic><topic>Photocatalysts</topic><topic>Synthesis (chemistry)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Oliveira, Kleber T</creatorcontrib><creatorcontrib>Miller, L. Zane</creatorcontrib><creatorcontrib>McQuade, D. Tyler</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Oliveira, Kleber T</au><au>Miller, L. Zane</au><au>McQuade, D. Tyler</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exploiting photooxygenations mediated by porphyrinoid photocatalysts under continuous flow conditions</atitle><jtitle>RSC advances</jtitle><date>2016-01-01</date><risdate>2016</risdate><volume>6</volume><issue>16</issue><spage>12717</spage><epage>12725</epage><pages>12717-12725</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>Photooxygenation reactions are a powerful synthetic tool to produce oxidized organic compounds; however, these reactions often exhibit experimental limitations including the production of complex mixtures that hinder desired product isolation and scale-up. Herein, we present a photocatalysed protocol under continuous flow conditions using a simple home built photoreactor and porphyrinoids as photocatalysts. Reaction conditions, long-term experiments, and scope demonstrate a protocol that is cost-effective, safe, reproducible and robust, thus allowing the production of relevant substituted naphthoquinones with interest in natural product synthesis and biological activity.
Photooxygenations of naphthols under continuous flow conditions using porphyrinoids as photocatalysts are described. Reaction conditions, long-term experiments and scope were performed, thus allowing the production of substituted naphthoquinones.</abstract><doi>10.1039/c6ra00285d</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2046-2069 |
ispartof | RSC advances, 2016-01, Vol.6 (16), p.12717-12725 |
issn | 2046-2069 2046-2069 |
language | eng |
recordid | cdi_rsc_primary_c6ra00285d |
source | Royal Society Of Chemistry Journals 2008- |
subjects | Biological Continuous flow Natural products Organic compounds Photocatalysis Photocatalysts Synthesis (chemistry) |
title | Exploiting photooxygenations mediated by porphyrinoid photocatalysts under continuous flow conditions |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T13%3A15%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_rsc_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Exploiting%20photooxygenations%20mediated%20by%20porphyrinoid%20photocatalysts%20under%20continuous%20flow%20conditions&rft.jtitle=RSC%20advances&rft.au=de%20Oliveira,%20Kleber%20T&rft.date=2016-01-01&rft.volume=6&rft.issue=16&rft.spage=12717&rft.epage=12725&rft.pages=12717-12725&rft.issn=2046-2069&rft.eissn=2046-2069&rft_id=info:doi/10.1039/c6ra00285d&rft_dat=%3Cproquest_rsc_p%3E1800481085%3C/proquest_rsc_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1800481085&rft_id=info:pmid/&rfr_iscdi=true |