Loading…
Synthesis of Allylbenzene Derivatives through sp3 C–H Bond Functionalization of Toluene Derivatives
Abstract An sp 3 C–H bond-transformation reaction of toluene substrates to afford the corresponding allylbenzene derivatives is described. Optimum conditions were identified as involving the use of tetrabutylammonium iodide and tert -butyl hydroperoxide at 80 °C.
Saved in:
Published in: | Synlett 2017-08, Vol.28 (13), p.1646-1648 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | 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-c1223-a4c42c3bb09fbd4745a3e194ee6a19a91eeb798245205dcd8392381d1dbb200c3 |
---|---|
cites | |
container_end_page | 1648 |
container_issue | 13 |
container_start_page | 1646 |
container_title | Synlett |
container_volume | 28 |
creator | Shahsavari, Fatemeh Abbasi, Alireza Ghazanfarpour-Darjani, Majid Ghafelebashi, Seyed Mehdi Daftari-Besheli, Majid |
description | Abstract
An sp
3
C–H bond-transformation reaction of toluene substrates to afford the corresponding allylbenzene derivatives is described. Optimum conditions were identified as involving the use of tetrabutylammonium iodide and
tert
-butyl hydroperoxide at 80 °C. |
doi_str_mv | 10.1055/s-0036-1588793 |
format | article |
fullrecord | <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1055_s_0036_1588793</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_s_0036_1588793</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1223-a4c42c3bb09fbd4745a3e194ee6a19a91eeb798245205dcd8392381d1dbb200c3</originalsourceid><addsrcrecordid>eNp1kE1OwzAQRi0EEqWwZe0LuPi3iZelUIpUiQVlbTnOhLhK4ypOKqUr7sANOQmN2hUSqxlpvvdJ8xC6Z3TCqFIPkVAqpoSpNE20uEAjJkVCONXTSzSi-nhSnMlrdBPjhlImU01HCN77ui0h-ohDgWdV1VcZ1AeoAT9B4_e29XuIuC2b0H2WOO4Env98fS_xY6hzvOhq1_pQ28of7LAMJetQdX_4W3RV2CrC3XmO0cfieT1fktXby-t8tiKOcS6IlU5yJ7KM6iLLZSKVFcC0BJhapq1mAFmiUy4Vpyp3eSo0FynLWZ5lnFInxmhy6nVNiLGBwuwav7VNbxg1gyQTzSDJnCUdAXIC2tLDFswmdM3xm_hf_hfg2mp3</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis of Allylbenzene Derivatives through sp3 C–H Bond Functionalization of Toluene Derivatives</title><source>Thieme - Connect here FIRST to enable access</source><creator>Shahsavari, Fatemeh ; Abbasi, Alireza ; Ghazanfarpour-Darjani, Majid ; Ghafelebashi, Seyed Mehdi ; Daftari-Besheli, Majid</creator><creatorcontrib>Shahsavari, Fatemeh ; Abbasi, Alireza ; Ghazanfarpour-Darjani, Majid ; Ghafelebashi, Seyed Mehdi ; Daftari-Besheli, Majid</creatorcontrib><description>Abstract
An sp
3
C–H bond-transformation reaction of toluene substrates to afford the corresponding allylbenzene derivatives is described. Optimum conditions were identified as involving the use of tetrabutylammonium iodide and
tert
-butyl hydroperoxide at 80 °C.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-0036-1588793</identifier><language>eng</language><publisher>Stuttgart · New York: Georg Thieme Verlag</publisher><subject>letter</subject><ispartof>Synlett, 2017-08, Vol.28 (13), p.1646-1648</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1223-a4c42c3bb09fbd4745a3e194ee6a19a91eeb798245205dcd8392381d1dbb200c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0036-1588793.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-0036-1588793$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,780,784,3017,3018,27924,27925,54559,54560</link.rule.ids></links><search><creatorcontrib>Shahsavari, Fatemeh</creatorcontrib><creatorcontrib>Abbasi, Alireza</creatorcontrib><creatorcontrib>Ghazanfarpour-Darjani, Majid</creatorcontrib><creatorcontrib>Ghafelebashi, Seyed Mehdi</creatorcontrib><creatorcontrib>Daftari-Besheli, Majid</creatorcontrib><title>Synthesis of Allylbenzene Derivatives through sp3 C–H Bond Functionalization of Toluene Derivatives</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract
An sp
3
C–H bond-transformation reaction of toluene substrates to afford the corresponding allylbenzene derivatives is described. Optimum conditions were identified as involving the use of tetrabutylammonium iodide and
tert
-butyl hydroperoxide at 80 °C.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kE1OwzAQRi0EEqWwZe0LuPi3iZelUIpUiQVlbTnOhLhK4ypOKqUr7sANOQmN2hUSqxlpvvdJ8xC6Z3TCqFIPkVAqpoSpNE20uEAjJkVCONXTSzSi-nhSnMlrdBPjhlImU01HCN77ui0h-ohDgWdV1VcZ1AeoAT9B4_e29XuIuC2b0H2WOO4Env98fS_xY6hzvOhq1_pQ28of7LAMJetQdX_4W3RV2CrC3XmO0cfieT1fktXby-t8tiKOcS6IlU5yJ7KM6iLLZSKVFcC0BJhapq1mAFmiUy4Vpyp3eSo0FynLWZ5lnFInxmhy6nVNiLGBwuwav7VNbxg1gyQTzSDJnCUdAXIC2tLDFswmdM3xm_hf_hfg2mp3</recordid><startdate>20170814</startdate><enddate>20170814</enddate><creator>Shahsavari, Fatemeh</creator><creator>Abbasi, Alireza</creator><creator>Ghazanfarpour-Darjani, Majid</creator><creator>Ghafelebashi, Seyed Mehdi</creator><creator>Daftari-Besheli, Majid</creator><general>Georg Thieme Verlag</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20170814</creationdate><title>Synthesis of Allylbenzene Derivatives through sp3 C–H Bond Functionalization of Toluene Derivatives</title><author>Shahsavari, Fatemeh ; Abbasi, Alireza ; Ghazanfarpour-Darjani, Majid ; Ghafelebashi, Seyed Mehdi ; Daftari-Besheli, Majid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1223-a4c42c3bb09fbd4745a3e194ee6a19a91eeb798245205dcd8392381d1dbb200c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shahsavari, Fatemeh</creatorcontrib><creatorcontrib>Abbasi, Alireza</creatorcontrib><creatorcontrib>Ghazanfarpour-Darjani, Majid</creatorcontrib><creatorcontrib>Ghafelebashi, Seyed Mehdi</creatorcontrib><creatorcontrib>Daftari-Besheli, Majid</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shahsavari, Fatemeh</au><au>Abbasi, Alireza</au><au>Ghazanfarpour-Darjani, Majid</au><au>Ghafelebashi, Seyed Mehdi</au><au>Daftari-Besheli, Majid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Allylbenzene Derivatives through sp3 C–H Bond Functionalization of Toluene Derivatives</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2017-08-14</date><risdate>2017</risdate><volume>28</volume><issue>13</issue><spage>1646</spage><epage>1648</epage><pages>1646-1648</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
An sp
3
C–H bond-transformation reaction of toluene substrates to afford the corresponding allylbenzene derivatives is described. Optimum conditions were identified as involving the use of tetrabutylammonium iodide and
tert
-butyl hydroperoxide at 80 °C.</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag</pub><doi>10.1055/s-0036-1588793</doi><tpages>3</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0936-5214 |
ispartof | Synlett, 2017-08, Vol.28 (13), p.1646-1648 |
issn | 0936-5214 1437-2096 |
language | eng |
recordid | cdi_crossref_primary_10_1055_s_0036_1588793 |
source | Thieme - Connect here FIRST to enable access |
subjects | letter |
title | Synthesis of Allylbenzene Derivatives through sp3 C–H Bond Functionalization of Toluene Derivatives |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T16%3A41%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-thieme_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20Allylbenzene%20Derivatives%20through%20sp3%20C%E2%80%93H%20Bond%20Functionalization%20of%20Toluene%20Derivatives&rft.jtitle=Synlett&rft.au=Shahsavari,%20Fatemeh&rft.date=2017-08-14&rft.volume=28&rft.issue=13&rft.spage=1646&rft.epage=1648&rft.pages=1646-1648&rft.issn=0936-5214&rft.eissn=1437-2096&rft_id=info:doi/10.1055/s-0036-1588793&rft_dat=%3Cthieme_cross%3E10_1055_s_0036_1588793%3C/thieme_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c1223-a4c42c3bb09fbd4745a3e194ee6a19a91eeb798245205dcd8392381d1dbb200c3%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 |