N-Phosphonyl/phosphinyl imines and group-assisted purification (GAP) chemistry/technology

The development of environmentally benign, operationally simple, and economically viable synthetic methodologies has been a great challenge in organic synthesis. Group-assisted purification (GAP) chemistry was established to enable the synthesis of organic compounds without using traditional purific...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Organic & biomolecular chemistry 2015-02, Vol.13 (6), p.1600-1617
Hauptverfasser: An, Guanghui, Seifert, Cole, Li, Guigen
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1617
container_issue 6
container_start_page 1600
container_title Organic & biomolecular chemistry
container_volume 13
creator An, Guanghui
Seifert, Cole
Li, Guigen
description The development of environmentally benign, operationally simple, and economically viable synthetic methodologies has been a great challenge in organic synthesis. Group-assisted purification (GAP) chemistry was established to enable the synthesis of organic compounds without using traditional purification technologies, such as column chromatography and recrystallization. This concept/technology should encourage the synthetic community to make more efforts on searching for environmentally benign reagents and reactions to reduce the waste generated from silica and solvents, particularly toxic solvents; also, to reduce production/synthesis expenses, manpower, and energy. This review will discuss the GAP concept/technology and related reactions that were mainly conducted in the PI's laboratories after 2010.
doi_str_mv 10.1039/c4ob02254h
format Article
fullrecord <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1039_C4OB02254H</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>25523061</sourcerecordid><originalsourceid>FETCH-LOGICAL-c394t-955d2d27512d1999329fcfcd5f553ff4405a2111775b8bacbafe187148d06b6c3</originalsourceid><addsrcrecordid>eNo9kDtPwzAURi0EoqWw8ANQRkAK8TOux1JBi1TRDjAwRY4fjVETR3Y65N8TWuh0j3SPvuEAcIvgE4JEZIr6EmLMaHUGxohynkJGxPmJMRyBqxi_IUSC5_QSjDBjmMAcjcHXe7qpfGwr3_S7rD2gGzBxtWtMTGSjk23w-zaVMbrYGZ20--CsU7JzvknuF7PNQ6IqUw_P0GedUVXjd37bX4MLK3fR3PzdCfh8ffmYL9PVevE2n61SRQTtUsGYxhpzhrBGQgiChVVWaWYZI9ZSCpnECCHOWTktpSqlNWjKEZ1qmJe5IhPweNxVwccYjC3a4GoZ-gLB4rdPMafr50Of5SDfHeV2X9ZGn9T_IOQHGKFhfg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>N-Phosphonyl/phosphinyl imines and group-assisted purification (GAP) chemistry/technology</title><source>MEDLINE</source><source>Royal Society Of Chemistry Journals</source><source>Alma/SFX Local Collection</source><creator>An, Guanghui ; Seifert, Cole ; Li, Guigen</creator><creatorcontrib>An, Guanghui ; Seifert, Cole ; Li, Guigen</creatorcontrib><description>The development of environmentally benign, operationally simple, and economically viable synthetic methodologies has been a great challenge in organic synthesis. Group-assisted purification (GAP) chemistry was established to enable the synthesis of organic compounds without using traditional purification technologies, such as column chromatography and recrystallization. This concept/technology should encourage the synthetic community to make more efforts on searching for environmentally benign reagents and reactions to reduce the waste generated from silica and solvents, particularly toxic solvents; also, to reduce production/synthesis expenses, manpower, and energy. This review will discuss the GAP concept/technology and related reactions that were mainly conducted in the PI's laboratories after 2010.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/c4ob02254h</identifier><identifier>PMID: 25523061</identifier><language>eng</language><publisher>England</publisher><subject>Imines - chemistry ; Imines - isolation &amp; purification ; Molecular Structure ; Organophosphorus Compounds - chemistry ; Organophosphorus Compounds - isolation &amp; purification</subject><ispartof>Organic &amp; biomolecular chemistry, 2015-02, Vol.13 (6), p.1600-1617</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-955d2d27512d1999329fcfcd5f553ff4405a2111775b8bacbafe187148d06b6c3</citedby><cites>FETCH-LOGICAL-c394t-955d2d27512d1999329fcfcd5f553ff4405a2111775b8bacbafe187148d06b6c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25523061$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>An, Guanghui</creatorcontrib><creatorcontrib>Seifert, Cole</creatorcontrib><creatorcontrib>Li, Guigen</creatorcontrib><title>N-Phosphonyl/phosphinyl imines and group-assisted purification (GAP) chemistry/technology</title><title>Organic &amp; biomolecular chemistry</title><addtitle>Org Biomol Chem</addtitle><description>The development of environmentally benign, operationally simple, and economically viable synthetic methodologies has been a great challenge in organic synthesis. Group-assisted purification (GAP) chemistry was established to enable the synthesis of organic compounds without using traditional purification technologies, such as column chromatography and recrystallization. This concept/technology should encourage the synthetic community to make more efforts on searching for environmentally benign reagents and reactions to reduce the waste generated from silica and solvents, particularly toxic solvents; also, to reduce production/synthesis expenses, manpower, and energy. This review will discuss the GAP concept/technology and related reactions that were mainly conducted in the PI's laboratories after 2010.</description><subject>Imines - chemistry</subject><subject>Imines - isolation &amp; purification</subject><subject>Molecular Structure</subject><subject>Organophosphorus Compounds - chemistry</subject><subject>Organophosphorus Compounds - isolation &amp; purification</subject><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kDtPwzAURi0EoqWw8ANQRkAK8TOux1JBi1TRDjAwRY4fjVETR3Y65N8TWuh0j3SPvuEAcIvgE4JEZIr6EmLMaHUGxohynkJGxPmJMRyBqxi_IUSC5_QSjDBjmMAcjcHXe7qpfGwr3_S7rD2gGzBxtWtMTGSjk23w-zaVMbrYGZ20--CsU7JzvknuF7PNQ6IqUw_P0GedUVXjd37bX4MLK3fR3PzdCfh8ffmYL9PVevE2n61SRQTtUsGYxhpzhrBGQgiChVVWaWYZI9ZSCpnECCHOWTktpSqlNWjKEZ1qmJe5IhPweNxVwccYjC3a4GoZ-gLB4rdPMafr50Of5SDfHeV2X9ZGn9T_IOQHGKFhfg</recordid><startdate>20150214</startdate><enddate>20150214</enddate><creator>An, Guanghui</creator><creator>Seifert, Cole</creator><creator>Li, Guigen</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20150214</creationdate><title>N-Phosphonyl/phosphinyl imines and group-assisted purification (GAP) chemistry/technology</title><author>An, Guanghui ; Seifert, Cole ; Li, Guigen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-955d2d27512d1999329fcfcd5f553ff4405a2111775b8bacbafe187148d06b6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Imines - chemistry</topic><topic>Imines - isolation &amp; purification</topic><topic>Molecular Structure</topic><topic>Organophosphorus Compounds - chemistry</topic><topic>Organophosphorus Compounds - isolation &amp; purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>An, Guanghui</creatorcontrib><creatorcontrib>Seifert, Cole</creatorcontrib><creatorcontrib>Li, Guigen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Organic &amp; biomolecular chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>An, Guanghui</au><au>Seifert, Cole</au><au>Li, Guigen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>N-Phosphonyl/phosphinyl imines and group-assisted purification (GAP) chemistry/technology</atitle><jtitle>Organic &amp; biomolecular chemistry</jtitle><addtitle>Org Biomol Chem</addtitle><date>2015-02-14</date><risdate>2015</risdate><volume>13</volume><issue>6</issue><spage>1600</spage><epage>1617</epage><pages>1600-1617</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>The development of environmentally benign, operationally simple, and economically viable synthetic methodologies has been a great challenge in organic synthesis. Group-assisted purification (GAP) chemistry was established to enable the synthesis of organic compounds without using traditional purification technologies, such as column chromatography and recrystallization. This concept/technology should encourage the synthetic community to make more efforts on searching for environmentally benign reagents and reactions to reduce the waste generated from silica and solvents, particularly toxic solvents; also, to reduce production/synthesis expenses, manpower, and energy. This review will discuss the GAP concept/technology and related reactions that were mainly conducted in the PI's laboratories after 2010.</abstract><cop>England</cop><pmid>25523061</pmid><doi>10.1039/c4ob02254h</doi><tpages>18</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1477-0520
ispartof Organic & biomolecular chemistry, 2015-02, Vol.13 (6), p.1600-1617
issn 1477-0520
1477-0539
language eng
recordid cdi_crossref_primary_10_1039_C4OB02254H
source MEDLINE; Royal Society Of Chemistry Journals; Alma/SFX Local Collection
subjects Imines - chemistry
Imines - isolation & purification
Molecular Structure
Organophosphorus Compounds - chemistry
Organophosphorus Compounds - isolation & purification
title N-Phosphonyl/phosphinyl imines and group-assisted purification (GAP) chemistry/technology
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T13%3A01%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=N-Phosphonyl/phosphinyl%20imines%20and%20group-assisted%20purification%20(GAP)%20chemistry/technology&rft.jtitle=Organic%20&%20biomolecular%20chemistry&rft.au=An,%20Guanghui&rft.date=2015-02-14&rft.volume=13&rft.issue=6&rft.spage=1600&rft.epage=1617&rft.pages=1600-1617&rft.issn=1477-0520&rft.eissn=1477-0539&rft_id=info:doi/10.1039/c4ob02254h&rft_dat=%3Cpubmed_cross%3E25523061%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/25523061&rfr_iscdi=true