Ytterbium Triflate Catalyzed Synthesis of Heterocycles
Abstract Ytterbium(III) triflate is an efficient and water-tolerant Lewis acid that has been used as a catalyst for a wide range of organic transformations. Various three-, four-, five-, and six-membered, as well as fused, heterocycles have been synthesized using ytterbium triflate as catalyst in bo...
Gespeichert in:
Veröffentlicht in: | Synthesis (Stuttgart) 2016-12, Vol.48 (24), p.4305-4346 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 4346 |
---|---|
container_issue | 24 |
container_start_page | 4305 |
container_title | Synthesis (Stuttgart) |
container_volume | 48 |
creator | Sakhuja, Rajeev Pericherla, Kasiviswanadharaju Bajaj, Kiran Khungar, Bharti Kumar, Anil |
description | Abstract
Ytterbium(III) triflate is an efficient and water-tolerant Lewis acid that has been used as a catalyst for a wide range of organic transformations. Various three-, four-, five-, and six-membered, as well as fused, heterocycles have been synthesized using ytterbium triflate as catalyst in both organic and aqueous solvents. The reaction conditions are relatively mild and the catalyst can be readily recovered from the reaction mixtures to be reused.
1 Introduction
2 Three-Membered Heterocycles
3 Four-Membered Heterocycles
4 Five-Membered Heterocycles
5 Six-Membered Heterocycles
6 Benzo-Fused Heterocycles
7 Non-benzenoid Fused Heterocycles
8 Spiroheterocycles
9 Bridged Heterocycles
10 Conclusion |
doi_str_mv | 10.1055/s-0036-1588321 |
format | Article |
fullrecord | <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1055_s_0036_1588321</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_s_0036_1588321</sourcerecordid><originalsourceid>FETCH-LOGICAL-c483t-f57d5949028d8482fe7515a576615ff73e161d39c415b4edda75bd063abb91363</originalsourceid><addsrcrecordid>eNp1jztPwzAUhS0EEqGwMucPuPjG8SMjioBWqsRAkWCynPhaTZU0yHaH8OtJ1a5MZzgPnY-QR2BLYEI8RcoYlxSE1ryAK5JByRUtgH1dk2y2Kqq0hltyF-OeMaYKXmVEfqeEoemOQ74Nne9twry2yfbTL7r8YzqkHcYu5qPPVzgnx3Zqe4z35MbbPuLDRRfk8_VlW6_o5v1tXT9vaFtqnqgXyomqrFihnS514VEJEFYoKUF4rziCBMertgTRlOicVaJxTHLbNBVwyRdked5twxhjQG9-QjfYMBlg5kRtojlRmwv1XKDnQtp1OKDZj8dwmB_-l_8DyPdX7g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Ytterbium Triflate Catalyzed Synthesis of Heterocycles</title><source>Thieme Connect Journals</source><creator>Sakhuja, Rajeev ; Pericherla, Kasiviswanadharaju ; Bajaj, Kiran ; Khungar, Bharti ; Kumar, Anil</creator><creatorcontrib>Sakhuja, Rajeev ; Pericherla, Kasiviswanadharaju ; Bajaj, Kiran ; Khungar, Bharti ; Kumar, Anil</creatorcontrib><description>Abstract
Ytterbium(III) triflate is an efficient and water-tolerant Lewis acid that has been used as a catalyst for a wide range of organic transformations. Various three-, four-, five-, and six-membered, as well as fused, heterocycles have been synthesized using ytterbium triflate as catalyst in both organic and aqueous solvents. The reaction conditions are relatively mild and the catalyst can be readily recovered from the reaction mixtures to be reused.
1 Introduction
2 Three-Membered Heterocycles
3 Four-Membered Heterocycles
4 Five-Membered Heterocycles
5 Six-Membered Heterocycles
6 Benzo-Fused Heterocycles
7 Non-benzenoid Fused Heterocycles
8 Spiroheterocycles
9 Bridged Heterocycles
10 Conclusion</description><identifier>ISSN: 0039-7881</identifier><identifier>EISSN: 1437-210X</identifier><identifier>DOI: 10.1055/s-0036-1588321</identifier><language>eng</language><publisher>Stuttgart · New York: Georg Thieme Verlag</publisher><subject>review</subject><ispartof>Synthesis (Stuttgart), 2016-12, Vol.48 (24), p.4305-4346</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-f57d5949028d8482fe7515a576615ff73e161d39c415b4edda75bd063abb91363</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-0036-1588321.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-0036-1588321$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3004,3005,27901,27902,54534,54535</link.rule.ids></links><search><creatorcontrib>Sakhuja, Rajeev</creatorcontrib><creatorcontrib>Pericherla, Kasiviswanadharaju</creatorcontrib><creatorcontrib>Bajaj, Kiran</creatorcontrib><creatorcontrib>Khungar, Bharti</creatorcontrib><creatorcontrib>Kumar, Anil</creatorcontrib><title>Ytterbium Triflate Catalyzed Synthesis of Heterocycles</title><title>Synthesis (Stuttgart)</title><addtitle>Synthesis</addtitle><description>Abstract
Ytterbium(III) triflate is an efficient and water-tolerant Lewis acid that has been used as a catalyst for a wide range of organic transformations. Various three-, four-, five-, and six-membered, as well as fused, heterocycles have been synthesized using ytterbium triflate as catalyst in both organic and aqueous solvents. The reaction conditions are relatively mild and the catalyst can be readily recovered from the reaction mixtures to be reused.
1 Introduction
2 Three-Membered Heterocycles
3 Four-Membered Heterocycles
4 Five-Membered Heterocycles
5 Six-Membered Heterocycles
6 Benzo-Fused Heterocycles
7 Non-benzenoid Fused Heterocycles
8 Spiroheterocycles
9 Bridged Heterocycles
10 Conclusion</description><subject>review</subject><issn>0039-7881</issn><issn>1437-210X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp1jztPwzAUhS0EEqGwMucPuPjG8SMjioBWqsRAkWCynPhaTZU0yHaH8OtJ1a5MZzgPnY-QR2BLYEI8RcoYlxSE1ryAK5JByRUtgH1dk2y2Kqq0hltyF-OeMaYKXmVEfqeEoemOQ74Nne9twry2yfbTL7r8YzqkHcYu5qPPVzgnx3Zqe4z35MbbPuLDRRfk8_VlW6_o5v1tXT9vaFtqnqgXyomqrFihnS514VEJEFYoKUF4rziCBMertgTRlOicVaJxTHLbNBVwyRdked5twxhjQG9-QjfYMBlg5kRtojlRmwv1XKDnQtp1OKDZj8dwmB_-l_8DyPdX7g</recordid><startdate>20161215</startdate><enddate>20161215</enddate><creator>Sakhuja, Rajeev</creator><creator>Pericherla, Kasiviswanadharaju</creator><creator>Bajaj, Kiran</creator><creator>Khungar, Bharti</creator><creator>Kumar, Anil</creator><general>Georg Thieme Verlag</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20161215</creationdate><title>Ytterbium Triflate Catalyzed Synthesis of Heterocycles</title><author>Sakhuja, Rajeev ; Pericherla, Kasiviswanadharaju ; Bajaj, Kiran ; Khungar, Bharti ; Kumar, Anil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-f57d5949028d8482fe7515a576615ff73e161d39c415b4edda75bd063abb91363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sakhuja, Rajeev</creatorcontrib><creatorcontrib>Pericherla, Kasiviswanadharaju</creatorcontrib><creatorcontrib>Bajaj, Kiran</creatorcontrib><creatorcontrib>Khungar, Bharti</creatorcontrib><creatorcontrib>Kumar, Anil</creatorcontrib><collection>CrossRef</collection><jtitle>Synthesis (Stuttgart)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sakhuja, Rajeev</au><au>Pericherla, Kasiviswanadharaju</au><au>Bajaj, Kiran</au><au>Khungar, Bharti</au><au>Kumar, Anil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ytterbium Triflate Catalyzed Synthesis of Heterocycles</atitle><jtitle>Synthesis (Stuttgart)</jtitle><addtitle>Synthesis</addtitle><date>2016-12-15</date><risdate>2016</risdate><volume>48</volume><issue>24</issue><spage>4305</spage><epage>4346</epage><pages>4305-4346</pages><issn>0039-7881</issn><eissn>1437-210X</eissn><abstract>Abstract
Ytterbium(III) triflate is an efficient and water-tolerant Lewis acid that has been used as a catalyst for a wide range of organic transformations. Various three-, four-, five-, and six-membered, as well as fused, heterocycles have been synthesized using ytterbium triflate as catalyst in both organic and aqueous solvents. The reaction conditions are relatively mild and the catalyst can be readily recovered from the reaction mixtures to be reused.
1 Introduction
2 Three-Membered Heterocycles
3 Four-Membered Heterocycles
4 Five-Membered Heterocycles
5 Six-Membered Heterocycles
6 Benzo-Fused Heterocycles
7 Non-benzenoid Fused Heterocycles
8 Spiroheterocycles
9 Bridged Heterocycles
10 Conclusion</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag</pub><doi>10.1055/s-0036-1588321</doi><tpages>42</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0039-7881 |
ispartof | Synthesis (Stuttgart), 2016-12, Vol.48 (24), p.4305-4346 |
issn | 0039-7881 1437-210X |
language | eng |
recordid | cdi_crossref_primary_10_1055_s_0036_1588321 |
source | Thieme Connect Journals |
subjects | review |
title | Ytterbium Triflate Catalyzed Synthesis of Heterocycles |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T03%3A26%3A09IST&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=Ytterbium%20Triflate%20Catalyzed%20Synthesis%20of%20Heterocycles&rft.jtitle=Synthesis%20(Stuttgart)&rft.au=Sakhuja,%20Rajeev&rft.date=2016-12-15&rft.volume=48&rft.issue=24&rft.spage=4305&rft.epage=4346&rft.pages=4305-4346&rft.issn=0039-7881&rft.eissn=1437-210X&rft_id=info:doi/10.1055/s-0036-1588321&rft_dat=%3Cthieme_cross%3E10_1055_s_0036_1588321%3C/thieme_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 |