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:
Bibliographic Details
Published in:Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2020-02, Vol.56 (2), p.145-160
Main Authors: Bugaenko, Dmitry I., Karchava, Alexander V., Yurovskaya, Marina A.
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