Loading…
The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 2. Catalysis of Michael and Biginelli reactions and nucleophilic addition at C=X and C≡X bonds
The second part of review is devoted to the catalytic role of DABCO in Michael and Biginelli reactions, as well as nucleophilic addition at C=X and C≡X bonds.
Saved in:
Published in: | Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2020-02, Vol.56 (2), p.145-160 |
---|---|
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-c2340-35f91dfbe3cee6e934686293fbf3d3324847633b9bdefb2691d4f7eb24f8bb0b3 |
---|---|
cites | cdi_FETCH-LOGICAL-c2340-35f91dfbe3cee6e934686293fbf3d3324847633b9bdefb2691d4f7eb24f8bb0b3 |
container_end_page | 160 |
container_issue | 2 |
container_start_page | 145 |
container_title | Chemistry of heterocyclic compounds (New York, N.Y. 1965) |
container_volume | 56 |
creator | Bugaenko, Dmitry I. Karchava, Alexander V. Yurovskaya, Marina A. |
description | The second part of review is devoted to the catalytic role of DABCO in Michael and Biginelli reactions, as well as nucleophilic addition at C=X and C≡X bonds. |
doi_str_mv | 10.1007/s10593-020-02637-0 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2392541472</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2392541472</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2340-35f91dfbe3cee6e934686293fbf3d3324847633b9bdefb2691d4f7eb24f8bb0b3</originalsourceid><addsrcrecordid>eNp9kU9u1TAQxi0EEo_CBVhZYkta2-P8Q2LRBgpIRWVRpO4s2xn3uQpJsP2Q3hE4BufhFpwEJ0GCFYvRaDy_7xtZHyHPOTvljNVnkbOyhYIJlquCumAPyI6XNRQNlPCQ7BhjbQFciMfkSYz3eax5I3fk580e6TcMUSc_-HSkk6Nvzi-661c0Hse0x-Qt1fM8eJuJaYwL4FOkRkdvX9LxYAec5n0W50mPPc2cHo6LbA7TjCF5jPSTDomKU9qty-hXm4_e7jUOq-rC3_kRh8HTgNpul5b3f_2p7nu_rKhOtHt9uwLdr-8_bqmZxj4-JY-cHiI--9NPyOfLtzfd--Lq-t2H7vyqsAIkK6B0Le-dQbCIFbYgq6YSLTjjoAcQspF1BWBa06MzosqwdDUaIV1jDDNwQl5svvmDXw8Yk7qfDmHMJ5WAVpSSy1pkSmyUDVOMAZ2ag_-iw1FxppbQ1BaayqGpNTTFsgg2UczweIfhr_V_VL8BkZKd3w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2392541472</pqid></control><display><type>article</type><title>The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 2. Catalysis of Michael and Biginelli reactions and nucleophilic addition at C=X and C≡X bonds</title><source>Springer Nature</source><creator>Bugaenko, Dmitry I. ; Karchava, Alexander V. ; Yurovskaya, Marina A.</creator><creatorcontrib>Bugaenko, Dmitry I. ; Karchava, Alexander V. ; Yurovskaya, Marina A.</creatorcontrib><description>The second part of review is devoted to the catalytic role of DABCO in Michael and Biginelli reactions, as well as nucleophilic addition at C=X and C≡X bonds.</description><identifier>ISSN: 0009-3122</identifier><identifier>EISSN: 1573-8353</identifier><identifier>DOI: 10.1007/s10593-020-02637-0</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Catalysis ; Chemistry ; Chemistry and Materials Science ; Organic Chemistry ; Pharmacy</subject><ispartof>Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2020-02, Vol.56 (2), p.145-160</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2340-35f91dfbe3cee6e934686293fbf3d3324847633b9bdefb2691d4f7eb24f8bb0b3</citedby><cites>FETCH-LOGICAL-c2340-35f91dfbe3cee6e934686293fbf3d3324847633b9bdefb2691d4f7eb24f8bb0b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Bugaenko, Dmitry I.</creatorcontrib><creatorcontrib>Karchava, Alexander V.</creatorcontrib><creatorcontrib>Yurovskaya, Marina A.</creatorcontrib><title>The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 2. Catalysis of Michael and Biginelli reactions and nucleophilic addition at C=X and C≡X bonds</title><title>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</title><addtitle>Chem Heterocycl Comp</addtitle><description>The second part of review is devoted to the catalytic role of DABCO in Michael and Biginelli reactions, as well as nucleophilic addition at C=X and C≡X bonds.</description><subject>Catalysis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Organic Chemistry</subject><subject>Pharmacy</subject><issn>0009-3122</issn><issn>1573-8353</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kU9u1TAQxi0EEo_CBVhZYkta2-P8Q2LRBgpIRWVRpO4s2xn3uQpJsP2Q3hE4BufhFpwEJ0GCFYvRaDy_7xtZHyHPOTvljNVnkbOyhYIJlquCumAPyI6XNRQNlPCQ7BhjbQFciMfkSYz3eax5I3fk580e6TcMUSc_-HSkk6Nvzi-661c0Hse0x-Qt1fM8eJuJaYwL4FOkRkdvX9LxYAec5n0W50mPPc2cHo6LbA7TjCF5jPSTDomKU9qty-hXm4_e7jUOq-rC3_kRh8HTgNpul5b3f_2p7nu_rKhOtHt9uwLdr-8_bqmZxj4-JY-cHiI--9NPyOfLtzfd--Lq-t2H7vyqsAIkK6B0Le-dQbCIFbYgq6YSLTjjoAcQspF1BWBa06MzosqwdDUaIV1jDDNwQl5svvmDXw8Yk7qfDmHMJ5WAVpSSy1pkSmyUDVOMAZ2ag_-iw1FxppbQ1BaayqGpNTTFsgg2UczweIfhr_V_VL8BkZKd3w</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Bugaenko, Dmitry I.</creator><creator>Karchava, Alexander V.</creator><creator>Yurovskaya, Marina A.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20200201</creationdate><title>The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 2. Catalysis of Michael and Biginelli reactions and nucleophilic addition at C=X and C≡X bonds</title><author>Bugaenko, Dmitry I. ; Karchava, Alexander V. ; Yurovskaya, Marina A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2340-35f91dfbe3cee6e934686293fbf3d3324847633b9bdefb2691d4f7eb24f8bb0b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Catalysis</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Organic Chemistry</topic><topic>Pharmacy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bugaenko, Dmitry I.</creatorcontrib><creatorcontrib>Karchava, Alexander V.</creatorcontrib><creatorcontrib>Yurovskaya, Marina A.</creatorcontrib><collection>CrossRef</collection><jtitle>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bugaenko, Dmitry I.</au><au>Karchava, Alexander V.</au><au>Yurovskaya, Marina A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 2. Catalysis of Michael and Biginelli reactions and nucleophilic addition at C=X and C≡X bonds</atitle><jtitle>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</jtitle><stitle>Chem Heterocycl Comp</stitle><date>2020-02-01</date><risdate>2020</risdate><volume>56</volume><issue>2</issue><spage>145</spage><epage>160</epage><pages>145-160</pages><issn>0009-3122</issn><eissn>1573-8353</eissn><abstract>The second part of review is devoted to the catalytic role of DABCO in Michael and Biginelli reactions, as well as nucleophilic addition at C=X and C≡X bonds.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10593-020-02637-0</doi><tpages>16</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-3122 |
ispartof | Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2020-02, Vol.56 (2), p.145-160 |
issn | 0009-3122 1573-8353 |
language | eng |
recordid | cdi_proquest_journals_2392541472 |
source | Springer Nature |
subjects | Catalysis Chemistry Chemistry and Materials Science Organic Chemistry Pharmacy |
title | The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 2. Catalysis of Michael and Biginelli reactions and nucleophilic addition at C=X and C≡X bonds |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T06%3A37%3A18IST&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=The%20versatility%20of%20DABCO:%20synthetic%20applications%20of%20its%20basic,%20nucleophilic,%20and%20catalytic%20properties%20Part%202.%20Catalysis%20of%20Michael%20and%20Biginelli%20reactions%20and%20nucleophilic%20addition%20at%20C=X%20and%20C%E2%89%A1X%20bonds&rft.jtitle=Chemistry%20of%20heterocyclic%20compounds%20(New%20York,%20N.Y.%201965)&rft.au=Bugaenko,%20Dmitry%20I.&rft.date=2020-02-01&rft.volume=56&rft.issue=2&rft.spage=145&rft.epage=160&rft.pages=145-160&rft.issn=0009-3122&rft.eissn=1573-8353&rft_id=info:doi/10.1007/s10593-020-02637-0&rft_dat=%3Cproquest_cross%3E2392541472%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2340-35f91dfbe3cee6e934686293fbf3d3324847633b9bdefb2691d4f7eb24f8bb0b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2392541472&rft_id=info:pmid/&rfr_iscdi=true |