Loading…

Convenient Route to Super-Expanded Calixpyrroles:  Synthesis of Calix[n]furano[m]pyrroles (n = 3, 4, 6, 8 and m = 2, 4)

meso-Alkylporphyrinogen-like cyclic oligomers containing furans and pyrroles have been synthesized by “3 + 2” and “4 + 2” approaches. Condensation of 5,5,10,10,15,15-hexaethyl-21,22-dioxatetrapyrromethane with 2,5-bis[(α-hydroxy-α,α-dimethyl)furan] resulted in the formation of cyclic hexamer and cyc...

Full description

Saved in:
Bibliographic Details
Published in:Organic letters 2000-10, Vol.2 (20), p.3115-3117
Main Authors: Arumugam, Nagarajan, Jang, Yong-Sung, Lee, Chang-Hee
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 3117
container_issue 20
container_start_page 3115
container_title Organic letters
container_volume 2
creator Arumugam, Nagarajan
Jang, Yong-Sung
Lee, Chang-Hee
description meso-Alkylporphyrinogen-like cyclic oligomers containing furans and pyrroles have been synthesized by “3 + 2” and “4 + 2” approaches. Condensation of 5,5,10,10,15,15-hexaethyl-21,22-dioxatetrapyrromethane with 2,5-bis[(α-hydroxy-α,α-dimethyl)furan] resulted in the formation of cyclic hexamer and cyclic dodcamer. Effects of catalysts, temperature, inorganic additives, solvent, and reaction concentration were examined.
doi_str_mv 10.1021/ol0063196
format article
fullrecord <record><control><sourceid>acs</sourceid><recordid>TN_cdi_acs_journals_10_1021_ol0063196</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>b615579547</sourcerecordid><originalsourceid>FETCH-LOGICAL-a115t-10a226d970cdfe377dc388d2c676debdf43660286e7655fd92409c719c60c5043</originalsourceid><addsrcrecordid>eNo9kE9Lw0AQxRdRsFYPfoO5CAqJzu4mu4ngQUL9AwXB6qmUsO5usCXdLdlE2ptXv6afxEi1p3n8ZnjzeIScUrykyOiVrxEFp7nYIwOaMh5LTNn-Tgs8JEchLBBpT_IB2RTefVg3t66FZ9-1FloPk25lm3i0XilnrIFC1fP1atM0vrbh-vvzCyYb177bMA_gq-166mZV1yjnp8vZ_ymcO7gBHkESgYggg94Olj1iPbo4JgeVqoM9-ZtD8no3eike4vHT_WNxO45VH7GNKSrGhMklalNZLqXRPMsM00IKY99MlXAhkGXCSpGmlclZgrmWNNcCdYoJH5Kzra_SoVz4rnH9t5Ji-dtXueuL_wCQ81th</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Convenient Route to Super-Expanded Calixpyrroles:  Synthesis of Calix[n]furano[m]pyrroles (n = 3, 4, 6, 8 and m = 2, 4)</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>Arumugam, Nagarajan ; Jang, Yong-Sung ; Lee, Chang-Hee</creator><creatorcontrib>Arumugam, Nagarajan ; Jang, Yong-Sung ; Lee, Chang-Hee</creatorcontrib><description>meso-Alkylporphyrinogen-like cyclic oligomers containing furans and pyrroles have been synthesized by “3 + 2” and “4 + 2” approaches. Condensation of 5,5,10,10,15,15-hexaethyl-21,22-dioxatetrapyrromethane with 2,5-bis[(α-hydroxy-α,α-dimethyl)furan] resulted in the formation of cyclic hexamer and cyclic dodcamer. Effects of catalysts, temperature, inorganic additives, solvent, and reaction concentration were examined.</description><identifier>ISSN: 1523-7060</identifier><identifier>EISSN: 1523-7052</identifier><identifier>DOI: 10.1021/ol0063196</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Organic letters, 2000-10, Vol.2 (20), p.3115-3117</ispartof><rights>Copyright © 2000 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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>Arumugam, Nagarajan</creatorcontrib><creatorcontrib>Jang, Yong-Sung</creatorcontrib><creatorcontrib>Lee, Chang-Hee</creatorcontrib><title>Convenient Route to Super-Expanded Calixpyrroles:  Synthesis of Calix[n]furano[m]pyrroles (n = 3, 4, 6, 8 and m = 2, 4)</title><title>Organic letters</title><addtitle>Org. Lett</addtitle><description>meso-Alkylporphyrinogen-like cyclic oligomers containing furans and pyrroles have been synthesized by “3 + 2” and “4 + 2” approaches. Condensation of 5,5,10,10,15,15-hexaethyl-21,22-dioxatetrapyrromethane with 2,5-bis[(α-hydroxy-α,α-dimethyl)furan] resulted in the formation of cyclic hexamer and cyclic dodcamer. Effects of catalysts, temperature, inorganic additives, solvent, and reaction concentration were examined.</description><issn>1523-7060</issn><issn>1523-7052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNo9kE9Lw0AQxRdRsFYPfoO5CAqJzu4mu4ngQUL9AwXB6qmUsO5usCXdLdlE2ptXv6afxEi1p3n8ZnjzeIScUrykyOiVrxEFp7nYIwOaMh5LTNn-Tgs8JEchLBBpT_IB2RTefVg3t66FZ9-1FloPk25lm3i0XilnrIFC1fP1atM0vrbh-vvzCyYb177bMA_gq-166mZV1yjnp8vZ_ymcO7gBHkESgYggg94Olj1iPbo4JgeVqoM9-ZtD8no3eike4vHT_WNxO45VH7GNKSrGhMklalNZLqXRPMsM00IKY99MlXAhkGXCSpGmlclZgrmWNNcCdYoJH5Kzra_SoVz4rnH9t5Ji-dtXueuL_wCQ81th</recordid><startdate>20001005</startdate><enddate>20001005</enddate><creator>Arumugam, Nagarajan</creator><creator>Jang, Yong-Sung</creator><creator>Lee, Chang-Hee</creator><general>American Chemical Society</general><scope/></search><sort><creationdate>20001005</creationdate><title>Convenient Route to Super-Expanded Calixpyrroles:  Synthesis of Calix[n]furano[m]pyrroles (n = 3, 4, 6, 8 and m = 2, 4)</title><author>Arumugam, Nagarajan ; Jang, Yong-Sung ; Lee, Chang-Hee</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a115t-10a226d970cdfe377dc388d2c676debdf43660286e7655fd92409c719c60c5043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arumugam, Nagarajan</creatorcontrib><creatorcontrib>Jang, Yong-Sung</creatorcontrib><creatorcontrib>Lee, Chang-Hee</creatorcontrib><jtitle>Organic letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arumugam, Nagarajan</au><au>Jang, Yong-Sung</au><au>Lee, Chang-Hee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Convenient Route to Super-Expanded Calixpyrroles:  Synthesis of Calix[n]furano[m]pyrroles (n = 3, 4, 6, 8 and m = 2, 4)</atitle><jtitle>Organic letters</jtitle><addtitle>Org. Lett</addtitle><date>2000-10-05</date><risdate>2000</risdate><volume>2</volume><issue>20</issue><spage>3115</spage><epage>3117</epage><pages>3115-3117</pages><issn>1523-7060</issn><eissn>1523-7052</eissn><abstract>meso-Alkylporphyrinogen-like cyclic oligomers containing furans and pyrroles have been synthesized by “3 + 2” and “4 + 2” approaches. Condensation of 5,5,10,10,15,15-hexaethyl-21,22-dioxatetrapyrromethane with 2,5-bis[(α-hydroxy-α,α-dimethyl)furan] resulted in the formation of cyclic hexamer and cyclic dodcamer. Effects of catalysts, temperature, inorganic additives, solvent, and reaction concentration were examined.</abstract><pub>American Chemical Society</pub><doi>10.1021/ol0063196</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1523-7060
ispartof Organic letters, 2000-10, Vol.2 (20), p.3115-3117
issn 1523-7060
1523-7052
language eng
recordid cdi_acs_journals_10_1021_ol0063196
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
title Convenient Route to Super-Expanded Calixpyrroles:  Synthesis of Calix[n]furano[m]pyrroles (n = 3, 4, 6, 8 and m = 2, 4)
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T16%3A51%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Convenient%20Route%20to%20Super-Expanded%20Calixpyrroles:%E2%80%89%20Synthesis%20of%20Calix%5Bn%5Dfurano%5Bm%5Dpyrroles%20(n%20=%203,%204,%206,%208%20and%20m%20=%202,%204)&rft.jtitle=Organic%20letters&rft.au=Arumugam,%20Nagarajan&rft.date=2000-10-05&rft.volume=2&rft.issue=20&rft.spage=3115&rft.epage=3117&rft.pages=3115-3117&rft.issn=1523-7060&rft.eissn=1523-7052&rft_id=info:doi/10.1021/ol0063196&rft_dat=%3Cacs%3Eb615579547%3C/acs%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a115t-10a226d970cdfe377dc388d2c676debdf43660286e7655fd92409c719c60c5043%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true