Loading…
Regio‐ and Enantioselective Iridium‐Catalyzed N‐Allylation of Indoles and Related Azoles with Racemic Branched Alkyl‐Substituted Allylic Acetates
Cyclometallated π‐allyliridium C,O‐benzoates modified with (S)‐tol‐BINAP, which are stable to air, water, and SiO2, catalyze highly enantioselective N‐allylations of indoles and related azoles. This reaction complements previously reported metal‐catalyzed indole allylations in that complete levels o...
Saved in:
Published in: | Angewandte Chemie 2019-06, Vol.131 (23), p.7844-7848 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites 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-c1629-dce96b0eb26b4069822c5aa144a707e55a9c9f2559cd359a0d6814f7c9743df33 |
---|---|
cites | cdi_FETCH-LOGICAL-c1629-dce96b0eb26b4069822c5aa144a707e55a9c9f2559cd359a0d6814f7c9743df33 |
container_end_page | 7848 |
container_issue | 23 |
container_start_page | 7844 |
container_title | Angewandte Chemie |
container_volume | 131 |
creator | Kim, Seung Wook Schempp, Tabitha T. Zbieg, Jason R. Stivala, Craig E. Krische, Michael J. |
description | Cyclometallated π‐allyliridium C,O‐benzoates modified with (S)‐tol‐BINAP, which are stable to air, water, and SiO2, catalyze highly enantioselective N‐allylations of indoles and related azoles. This reaction complements previously reported metal‐catalyzed indole allylations in that complete levels of N versus C3 and branched versus linear regioselectivity are observed.
Immer an der richtigen Stelle: Cyclometallierte und mit (S)‐tol‐BINAP modifizierte π‐Allyliridium‐C,O‐benzoate – stabil in Luft, Wasser und SiO2 – katalysieren hoch enantioselektiv N‐Allylierungen von Indolen und anderen Azolen. Die Reaktion ergänzt vorherige metallkatalysierte Indol‐Allylierungen insofern, als vollständige Regioselektivität in Bezug auf N vs. C3 und verzweigt vs. linear erreicht wird. |
doi_str_mv | 10.1002/ange.201902799 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2229551056</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2229551056</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1629-dce96b0eb26b4069822c5aa144a707e55a9c9f2559cd359a0d6814f7c9743df33</originalsourceid><addsrcrecordid>eNqFkLFOwzAURS0EEqWwMkdiTrGdOKnHUJVSqSpSgTlynJfWxXUgTqjSiU9g5ff4EpwWwchk-b1zz5MuQpcEDwjG9FqYJQwoJhzTmPMj1COMEj-IWXyMehiHoT-kIT9FZ9auMcaRo3rocwFLVX69f3jC5N7YCFOr0oIGWas38KaVylWzcfuRqIVud5B7c_dLtG61cKjxysKbmrzUYPeKBbi5o5LdfrRV9cpbCAkbJb2bShi56pb6udVO89BktlZ1sw90SgclEmpnsOfopBDawsXP20dPt-PH0Z0_u59MR8nMlySi3M8l8CjDkNEoC3HEh5RKJgQJQxHjGBgTXPKCMsZlHjAucB4NSVjEksdhkBdB0EdXB-9LVb42YOt0XTaVcSdTSilnjGAWOWpwoGRVWltBkb5UaiOqNiU47epPu_rT3_pdgB8CW6Wh_YdOk_lk_Jf9BtXQj4g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2229551056</pqid></control><display><type>article</type><title>Regio‐ and Enantioselective Iridium‐Catalyzed N‐Allylation of Indoles and Related Azoles with Racemic Branched Alkyl‐Substituted Allylic Acetates</title><source>Wiley</source><creator>Kim, Seung Wook ; Schempp, Tabitha T. ; Zbieg, Jason R. ; Stivala, Craig E. ; Krische, Michael J.</creator><creatorcontrib>Kim, Seung Wook ; Schempp, Tabitha T. ; Zbieg, Jason R. ; Stivala, Craig E. ; Krische, Michael J.</creatorcontrib><description>Cyclometallated π‐allyliridium C,O‐benzoates modified with (S)‐tol‐BINAP, which are stable to air, water, and SiO2, catalyze highly enantioselective N‐allylations of indoles and related azoles. This reaction complements previously reported metal‐catalyzed indole allylations in that complete levels of N versus C3 and branched versus linear regioselectivity are observed.
Immer an der richtigen Stelle: Cyclometallierte und mit (S)‐tol‐BINAP modifizierte π‐Allyliridium‐C,O‐benzoate – stabil in Luft, Wasser und SiO2 – katalysieren hoch enantioselektiv N‐Allylierungen von Indolen und anderen Azolen. Die Reaktion ergänzt vorherige metallkatalysierte Indol‐Allylierungen insofern, als vollständige Regioselektivität in Bezug auf N vs. C3 und verzweigt vs. linear erreicht wird.</description><identifier>ISSN: 0044-8249</identifier><identifier>EISSN: 1521-3757</identifier><identifier>DOI: 10.1002/ange.201902799</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Acetates ; Acetic acid ; Allyl compounds ; Allylische Alkylierung ; Aminierung ; Azoles ; Benzoates ; Benzoic acid ; C-N-Bindungsbildung ; Chemical reactions ; Chemistry ; Enantiomers ; Enantioselektive Reaktionen ; Heterocyclic compounds ; Indoles ; Iridium ; Regioselectivity ; Silicon dioxide</subject><ispartof>Angewandte Chemie, 2019-06, Vol.131 (23), p.7844-7848</ispartof><rights>2019 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1629-dce96b0eb26b4069822c5aa144a707e55a9c9f2559cd359a0d6814f7c9743df33</citedby><cites>FETCH-LOGICAL-c1629-dce96b0eb26b4069822c5aa144a707e55a9c9f2559cd359a0d6814f7c9743df33</cites><orcidid>0000-0002-5024-6346 ; 0000-0002-2897-8911 ; 0000-0001-8418-9709</orcidid></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>Kim, Seung Wook</creatorcontrib><creatorcontrib>Schempp, Tabitha T.</creatorcontrib><creatorcontrib>Zbieg, Jason R.</creatorcontrib><creatorcontrib>Stivala, Craig E.</creatorcontrib><creatorcontrib>Krische, Michael J.</creatorcontrib><title>Regio‐ and Enantioselective Iridium‐Catalyzed N‐Allylation of Indoles and Related Azoles with Racemic Branched Alkyl‐Substituted Allylic Acetates</title><title>Angewandte Chemie</title><description>Cyclometallated π‐allyliridium C,O‐benzoates modified with (S)‐tol‐BINAP, which are stable to air, water, and SiO2, catalyze highly enantioselective N‐allylations of indoles and related azoles. This reaction complements previously reported metal‐catalyzed indole allylations in that complete levels of N versus C3 and branched versus linear regioselectivity are observed.
Immer an der richtigen Stelle: Cyclometallierte und mit (S)‐tol‐BINAP modifizierte π‐Allyliridium‐C,O‐benzoate – stabil in Luft, Wasser und SiO2 – katalysieren hoch enantioselektiv N‐Allylierungen von Indolen und anderen Azolen. Die Reaktion ergänzt vorherige metallkatalysierte Indol‐Allylierungen insofern, als vollständige Regioselektivität in Bezug auf N vs. C3 und verzweigt vs. linear erreicht wird.</description><subject>Acetates</subject><subject>Acetic acid</subject><subject>Allyl compounds</subject><subject>Allylische Alkylierung</subject><subject>Aminierung</subject><subject>Azoles</subject><subject>Benzoates</subject><subject>Benzoic acid</subject><subject>C-N-Bindungsbildung</subject><subject>Chemical reactions</subject><subject>Chemistry</subject><subject>Enantiomers</subject><subject>Enantioselektive Reaktionen</subject><subject>Heterocyclic compounds</subject><subject>Indoles</subject><subject>Iridium</subject><subject>Regioselectivity</subject><subject>Silicon dioxide</subject><issn>0044-8249</issn><issn>1521-3757</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkLFOwzAURS0EEqWwMkdiTrGdOKnHUJVSqSpSgTlynJfWxXUgTqjSiU9g5ff4EpwWwchk-b1zz5MuQpcEDwjG9FqYJQwoJhzTmPMj1COMEj-IWXyMehiHoT-kIT9FZ9auMcaRo3rocwFLVX69f3jC5N7YCFOr0oIGWas38KaVylWzcfuRqIVud5B7c_dLtG61cKjxysKbmrzUYPeKBbi5o5LdfrRV9cpbCAkbJb2bShi56pb6udVO89BktlZ1sw90SgclEmpnsOfopBDawsXP20dPt-PH0Z0_u59MR8nMlySi3M8l8CjDkNEoC3HEh5RKJgQJQxHjGBgTXPKCMsZlHjAucB4NSVjEksdhkBdB0EdXB-9LVb42YOt0XTaVcSdTSilnjGAWOWpwoGRVWltBkb5UaiOqNiU47epPu_rT3_pdgB8CW6Wh_YdOk_lk_Jf9BtXQj4g</recordid><startdate>20190603</startdate><enddate>20190603</enddate><creator>Kim, Seung Wook</creator><creator>Schempp, Tabitha T.</creator><creator>Zbieg, Jason R.</creator><creator>Stivala, Craig E.</creator><creator>Krische, Michael J.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-5024-6346</orcidid><orcidid>https://orcid.org/0000-0002-2897-8911</orcidid><orcidid>https://orcid.org/0000-0001-8418-9709</orcidid></search><sort><creationdate>20190603</creationdate><title>Regio‐ and Enantioselective Iridium‐Catalyzed N‐Allylation of Indoles and Related Azoles with Racemic Branched Alkyl‐Substituted Allylic Acetates</title><author>Kim, Seung Wook ; Schempp, Tabitha T. ; Zbieg, Jason R. ; Stivala, Craig E. ; Krische, Michael J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1629-dce96b0eb26b4069822c5aa144a707e55a9c9f2559cd359a0d6814f7c9743df33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acetates</topic><topic>Acetic acid</topic><topic>Allyl compounds</topic><topic>Allylische Alkylierung</topic><topic>Aminierung</topic><topic>Azoles</topic><topic>Benzoates</topic><topic>Benzoic acid</topic><topic>C-N-Bindungsbildung</topic><topic>Chemical reactions</topic><topic>Chemistry</topic><topic>Enantiomers</topic><topic>Enantioselektive Reaktionen</topic><topic>Heterocyclic compounds</topic><topic>Indoles</topic><topic>Iridium</topic><topic>Regioselectivity</topic><topic>Silicon dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Seung Wook</creatorcontrib><creatorcontrib>Schempp, Tabitha T.</creatorcontrib><creatorcontrib>Zbieg, Jason R.</creatorcontrib><creatorcontrib>Stivala, Craig E.</creatorcontrib><creatorcontrib>Krische, Michael J.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Angewandte Chemie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Seung Wook</au><au>Schempp, Tabitha T.</au><au>Zbieg, Jason R.</au><au>Stivala, Craig E.</au><au>Krische, Michael J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regio‐ and Enantioselective Iridium‐Catalyzed N‐Allylation of Indoles and Related Azoles with Racemic Branched Alkyl‐Substituted Allylic Acetates</atitle><jtitle>Angewandte Chemie</jtitle><date>2019-06-03</date><risdate>2019</risdate><volume>131</volume><issue>23</issue><spage>7844</spage><epage>7848</epage><pages>7844-7848</pages><issn>0044-8249</issn><eissn>1521-3757</eissn><abstract>Cyclometallated π‐allyliridium C,O‐benzoates modified with (S)‐tol‐BINAP, which are stable to air, water, and SiO2, catalyze highly enantioselective N‐allylations of indoles and related azoles. This reaction complements previously reported metal‐catalyzed indole allylations in that complete levels of N versus C3 and branched versus linear regioselectivity are observed.
Immer an der richtigen Stelle: Cyclometallierte und mit (S)‐tol‐BINAP modifizierte π‐Allyliridium‐C,O‐benzoate – stabil in Luft, Wasser und SiO2 – katalysieren hoch enantioselektiv N‐Allylierungen von Indolen und anderen Azolen. Die Reaktion ergänzt vorherige metallkatalysierte Indol‐Allylierungen insofern, als vollständige Regioselektivität in Bezug auf N vs. C3 und verzweigt vs. linear erreicht wird.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ange.201902799</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-5024-6346</orcidid><orcidid>https://orcid.org/0000-0002-2897-8911</orcidid><orcidid>https://orcid.org/0000-0001-8418-9709</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0044-8249 |
ispartof | Angewandte Chemie, 2019-06, Vol.131 (23), p.7844-7848 |
issn | 0044-8249 1521-3757 |
language | eng |
recordid | cdi_proquest_journals_2229551056 |
source | Wiley |
subjects | Acetates Acetic acid Allyl compounds Allylische Alkylierung Aminierung Azoles Benzoates Benzoic acid C-N-Bindungsbildung Chemical reactions Chemistry Enantiomers Enantioselektive Reaktionen Heterocyclic compounds Indoles Iridium Regioselectivity Silicon dioxide |
title | Regio‐ and Enantioselective Iridium‐Catalyzed N‐Allylation of Indoles and Related Azoles with Racemic Branched Alkyl‐Substituted Allylic Acetates |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T09%3A18%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Regio%E2%80%90%20and%20Enantioselective%20Iridium%E2%80%90Catalyzed%20N%E2%80%90Allylation%20of%20Indoles%20and%20Related%20Azoles%20with%20Racemic%20Branched%20Alkyl%E2%80%90Substituted%20Allylic%20Acetates&rft.jtitle=Angewandte%20Chemie&rft.au=Kim,%20Seung%20Wook&rft.date=2019-06-03&rft.volume=131&rft.issue=23&rft.spage=7844&rft.epage=7848&rft.pages=7844-7848&rft.issn=0044-8249&rft.eissn=1521-3757&rft_id=info:doi/10.1002/ange.201902799&rft_dat=%3Cproquest_cross%3E2229551056%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c1629-dce96b0eb26b4069822c5aa144a707e55a9c9f2559cd359a0d6814f7c9743df33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2229551056&rft_id=info:pmid/&rfr_iscdi=true |