Polyazaphosphorus macrocycles: Synthesis, reactivity, complexation

Polyazaphosphorus macrocycles: Synthesis, reactivity, complexation

A general synthesis of various polyazaphosphorus macrocycles involving [1 + 1], [2 + 2], or [3 + 3] cyclocondensations is reviewed, as well as the attempted synthesis of cryptands. Selective reduction (imino functions) methylation (PS groups), silylation (PO groups) are reported. Preparations of s...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Heteroatom chemistry 1991-02, Vol.2 (1), p.45-54
Hauptverfasser: Majoral, Jean-Pierre, Badri, Meryam, Caminade, Anne-Marie
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 54
container_issue 1
container_start_page 45
container_title Heteroatom chemistry
container_volume 2
creator Majoral, Jean-Pierre
Badri, Meryam
Caminade, Anne-Marie
description A general synthesis of various polyazaphosphorus macrocycles involving [1 + 1], [2 + 2], or [3 + 3] cyclocondensations is reviewed, as well as the attempted synthesis of cryptands. Selective reduction (imino functions) methylation (PS groups), silylation (PO groups) are reported. Preparations of some macrocycle complexes are described.
doi_str_mv 10.1002/hc.520020107
format Article
fullrecord <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_hc_520020107</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>HC520020107</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2327-d2a9517d371131a6163bfcd5e2dc57335da85735a1b20ae36024f935844908a03</originalsourceid><addsrcrecordid>eNp9j1FLwzAUhYMoOKdv_oD-gFVzk6ZpfXPDbcJQwcnAl3CXpjTarSOpuvrrzZgMn3y4nPPwncs5hFwCvQJK2XWlrwQLhgKVR6QHNM_iYOF45xMWS0j5KTnz_o1SgCTPemT41NQdfuOmanw49-GjFWrX6E7Xxt9Ez926rYy3fhA5g7q1n7btBpFuVpvabLG1zfqcnJRYe3Pxq33yMr6bj6bx7HFyP7qdxZpxJuOCYS5AFlwCcMA0dFmWuhCGFVpIzkWBWVCBsGQUDU8pS8qciyxJcpoh5X0y2P8N9bx3plQbZ1foOgVU7farSqvD_oCLPf5la9P9y6rp6G8u3uesb832kEP3rlLJpVCLh4kaysVcvnKuxvwHv49r3g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Polyazaphosphorus macrocycles: Synthesis, reactivity, complexation</title><source>Alma/SFX Local Collection</source><creator>Majoral, Jean-Pierre ; Badri, Meryam ; Caminade, Anne-Marie</creator><creatorcontrib>Majoral, Jean-Pierre ; Badri, Meryam ; Caminade, Anne-Marie</creatorcontrib><description>A general synthesis of various polyazaphosphorus macrocycles involving [1 + 1], [2 + 2], or [3 + 3] cyclocondensations is reviewed, as well as the attempted synthesis of cryptands. Selective reduction (imino functions) methylation (PS groups), silylation (PO groups) are reported. Preparations of some macrocycle complexes are described.</description><identifier>ISSN: 1042-7163</identifier><identifier>EISSN: 1098-1071</identifier><identifier>DOI: 10.1002/hc.520020107</identifier><language>eng</language><publisher>Florida: VCH Publishers, Inc</publisher><ispartof>Heteroatom chemistry, 1991-02, Vol.2 (1), p.45-54</ispartof><rights>Copyright © 1991 VCH Publishers, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2327-d2a9517d371131a6163bfcd5e2dc57335da85735a1b20ae36024f935844908a03</citedby><cites>FETCH-LOGICAL-c2327-d2a9517d371131a6163bfcd5e2dc57335da85735a1b20ae36024f935844908a03</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></links><search><creatorcontrib>Majoral, Jean-Pierre</creatorcontrib><creatorcontrib>Badri, Meryam</creatorcontrib><creatorcontrib>Caminade, Anne-Marie</creatorcontrib><title>Polyazaphosphorus macrocycles: Synthesis, reactivity, complexation</title><title>Heteroatom chemistry</title><addtitle>Heteroatom Chem</addtitle><description>A general synthesis of various polyazaphosphorus macrocycles involving [1 + 1], [2 + 2], or [3 + 3] cyclocondensations is reviewed, as well as the attempted synthesis of cryptands. Selective reduction (imino functions) methylation (PS groups), silylation (PO groups) are reported. Preparations of some macrocycle complexes are described.</description><issn>1042-7163</issn><issn>1098-1071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNp9j1FLwzAUhYMoOKdv_oD-gFVzk6ZpfXPDbcJQwcnAl3CXpjTarSOpuvrrzZgMn3y4nPPwncs5hFwCvQJK2XWlrwQLhgKVR6QHNM_iYOF45xMWS0j5KTnz_o1SgCTPemT41NQdfuOmanw49-GjFWrX6E7Xxt9Ez926rYy3fhA5g7q1n7btBpFuVpvabLG1zfqcnJRYe3Pxq33yMr6bj6bx7HFyP7qdxZpxJuOCYS5AFlwCcMA0dFmWuhCGFVpIzkWBWVCBsGQUDU8pS8qciyxJcpoh5X0y2P8N9bx3plQbZ1foOgVU7farSqvD_oCLPf5la9P9y6rp6G8u3uesb832kEP3rlLJpVCLh4kaysVcvnKuxvwHv49r3g</recordid><startdate>199102</startdate><enddate>199102</enddate><creator>Majoral, Jean-Pierre</creator><creator>Badri, Meryam</creator><creator>Caminade, Anne-Marie</creator><general>VCH Publishers, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199102</creationdate><title>Polyazaphosphorus macrocycles: Synthesis, reactivity, complexation</title><author>Majoral, Jean-Pierre ; Badri, Meryam ; Caminade, Anne-Marie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2327-d2a9517d371131a6163bfcd5e2dc57335da85735a1b20ae36024f935844908a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Majoral, Jean-Pierre</creatorcontrib><creatorcontrib>Badri, Meryam</creatorcontrib><creatorcontrib>Caminade, Anne-Marie</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Heteroatom chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Majoral, Jean-Pierre</au><au>Badri, Meryam</au><au>Caminade, Anne-Marie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polyazaphosphorus macrocycles: Synthesis, reactivity, complexation</atitle><jtitle>Heteroatom chemistry</jtitle><addtitle>Heteroatom Chem</addtitle><date>1991-02</date><risdate>1991</risdate><volume>2</volume><issue>1</issue><spage>45</spage><epage>54</epage><pages>45-54</pages><issn>1042-7163</issn><eissn>1098-1071</eissn><abstract>A general synthesis of various polyazaphosphorus macrocycles involving [1 + 1], [2 + 2], or [3 + 3] cyclocondensations is reviewed, as well as the attempted synthesis of cryptands. Selective reduction (imino functions) methylation (PS groups), silylation (PO groups) are reported. Preparations of some macrocycle complexes are described.</abstract><cop>Florida</cop><pub>VCH Publishers, Inc</pub><doi>10.1002/hc.520020107</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1042-7163
ispartof Heteroatom chemistry, 1991-02, Vol.2 (1), p.45-54
issn 1042-7163
1098-1071
language eng
recordid cdi_crossref_primary_10_1002_hc_520020107
source Alma/SFX Local Collection
title Polyazaphosphorus macrocycles: Synthesis, reactivity, complexation
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T16%3A01%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Polyazaphosphorus%20macrocycles:%20Synthesis,%20reactivity,%20complexation&rft.jtitle=Heteroatom%20chemistry&rft.au=Majoral,%20Jean-Pierre&rft.date=1991-02&rft.volume=2&rft.issue=1&rft.spage=45&rft.epage=54&rft.pages=45-54&rft.issn=1042-7163&rft.eissn=1098-1071&rft_id=info:doi/10.1002/hc.520020107&rft_dat=%3Cwiley_cross%3EHC520020107%3C/wiley_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/&rfr_iscdi=true