Loading…
Ligand effects, solvent cooperation, and large kinetic solvent deuterium isotope effects in gold(I)-catalyzed intramolecular alkene hydroamination
Kinetic studies on the intramolecular hydroamination of protected variants of 2,2-diphenylpent-4-en-1-amine were carried out under a variety of conditions with cationic gold catalysts supported by phosphine ligands. The impact of ligand on gold, protecting group on nitrogen, and solvent and additive...
Saved in:
Published in: | Beilstein journal of organic chemistry 2024-02, Vol.20 (1), p.479-496 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c404t-fe7925f38652968d52e67508c8aa4941094dbe5b91af00e98d1d71a8283e73f73 |
container_end_page | 496 |
container_issue | 1 |
container_start_page | 479 |
container_title | Beilstein journal of organic chemistry |
container_volume | 20 |
creator | Lan, Ruichen Yager, Brock Jee, Yoonsun Day, Cynthia S Jones, Amanda C |
description | Kinetic studies on the intramolecular hydroamination of protected variants of 2,2-diphenylpent-4-en-1-amine were carried out under a variety of conditions with cationic gold catalysts supported by phosphine ligands. The impact of ligand on gold, protecting group on nitrogen, and solvent and additive on reaction rates was determined. The most effective reactions utilized more Lewis basic ureas, and more electron-withdrawing phosphines. A DCM/alcohol cooperative effect was quantified, and a continuum of isotope effects was measured with low KIE's in the absence of deuterated alcoholic solvent, increasing to large solvent KIE's when comparing reactions in pure MeOH to those in pure MeOH-
. The effects are interpreted both within the context of a classic gold π-activation/protodeauration mechanism and a general acid-catalyzed mechanism without intermediate gold alkyls. |
doi_str_mv | 10.3762/bjoc.20.43 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_8d601c5d30e8401b822e8cc76ca0d2cd</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_8d601c5d30e8401b822e8cc76ca0d2cd</doaj_id><sourcerecordid>2937704433</sourcerecordid><originalsourceid>FETCH-LOGICAL-c404t-fe7925f38652968d52e67508c8aa4941094dbe5b91af00e98d1d71a8283e73f73</originalsourceid><addsrcrecordid>eNpVksFu1DAQQCMEoqVw4QNQjgU1y8R2HOdUoarASitxgbPl2JPUWydebKfS8hl8cZNuu2pPtsbPb2bsybKPJaxozcnXduv1isCK0VfZaSk4FBVt6tfP9ifZuxi3AAw48LfZCRWMQcnFafZ_Y3s1mhy7DnWKF3n07g7HlGvvdxhUsn68yBfCqdBjfmtHTFYfMYNTwmCnIbfRp_nKkym3Y957Z87XnwutknL7f2jmYApq8A71NPty5W5xxPxmb4JXgx0f0r3P3nTKRfzwuJ5lf75f_776WWx-_VhffdsUmgFLRYd1Q6qOCl6RhgtTEeR1BUILpVjDSmiYabFqm1J1ANgIU5q6VIIIijXtanqWrQ9e49VW7oIdVNhLr6x8CPjQSxXmXh1KYTiUujIUUMwP1wpCUGhdc63AEG1m1-XBtZvaAY3GpU_3QvryZLQ3svd3ci6znL8FZsP5oyH4vxPGJAcbNTqnRvRTlKShdQ2MUTqjXw6oDj7GgN0xTwlymQi5TIQkINkCf3pe2RF9GgF6D87WtZw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2937704433</pqid></control><display><type>article</type><title>Ligand effects, solvent cooperation, and large kinetic solvent deuterium isotope effects in gold(I)-catalyzed intramolecular alkene hydroamination</title><source>PubMed Central</source><source>ProQuest Publicly Available Content database</source><creator>Lan, Ruichen ; Yager, Brock ; Jee, Yoonsun ; Day, Cynthia S ; Jones, Amanda C</creator><creatorcontrib>Lan, Ruichen ; Yager, Brock ; Jee, Yoonsun ; Day, Cynthia S ; Jones, Amanda C</creatorcontrib><description>Kinetic studies on the intramolecular hydroamination of protected variants of 2,2-diphenylpent-4-en-1-amine were carried out under a variety of conditions with cationic gold catalysts supported by phosphine ligands. The impact of ligand on gold, protecting group on nitrogen, and solvent and additive on reaction rates was determined. The most effective reactions utilized more Lewis basic ureas, and more electron-withdrawing phosphines. A DCM/alcohol cooperative effect was quantified, and a continuum of isotope effects was measured with low KIE's in the absence of deuterated alcoholic solvent, increasing to large solvent KIE's when comparing reactions in pure MeOH to those in pure MeOH-
. The effects are interpreted both within the context of a classic gold π-activation/protodeauration mechanism and a general acid-catalyzed mechanism without intermediate gold alkyls.</description><identifier>ISSN: 1860-5397</identifier><identifier>EISSN: 1860-5397</identifier><identifier>DOI: 10.3762/bjoc.20.43</identifier><identifier>PMID: 38440168</identifier><language>eng</language><publisher>Germany: Beilstein-Institut</publisher><subject>alkene hydroamination ; Chemistry ; Full Research Paper ; general acid catalysis ; gold catalysis ; isotope effect ; phosphine ligand effect ; solvent effect</subject><ispartof>Beilstein journal of organic chemistry, 2024-02, Vol.20 (1), p.479-496</ispartof><rights>Copyright © 2024, Lan et al.</rights><rights>Copyright © 2024, Lan et al. 2024 Lan et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c404t-fe7925f38652968d52e67508c8aa4941094dbe5b91af00e98d1d71a8283e73f73</cites><orcidid>0000-0001-7445-8311 ; 0009-0008-9159-3791</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10910400/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10910400/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,36990,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38440168$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lan, Ruichen</creatorcontrib><creatorcontrib>Yager, Brock</creatorcontrib><creatorcontrib>Jee, Yoonsun</creatorcontrib><creatorcontrib>Day, Cynthia S</creatorcontrib><creatorcontrib>Jones, Amanda C</creatorcontrib><title>Ligand effects, solvent cooperation, and large kinetic solvent deuterium isotope effects in gold(I)-catalyzed intramolecular alkene hydroamination</title><title>Beilstein journal of organic chemistry</title><addtitle>Beilstein J Org Chem</addtitle><description>Kinetic studies on the intramolecular hydroamination of protected variants of 2,2-diphenylpent-4-en-1-amine were carried out under a variety of conditions with cationic gold catalysts supported by phosphine ligands. The impact of ligand on gold, protecting group on nitrogen, and solvent and additive on reaction rates was determined. The most effective reactions utilized more Lewis basic ureas, and more electron-withdrawing phosphines. A DCM/alcohol cooperative effect was quantified, and a continuum of isotope effects was measured with low KIE's in the absence of deuterated alcoholic solvent, increasing to large solvent KIE's when comparing reactions in pure MeOH to those in pure MeOH-
. The effects are interpreted both within the context of a classic gold π-activation/protodeauration mechanism and a general acid-catalyzed mechanism without intermediate gold alkyls.</description><subject>alkene hydroamination</subject><subject>Chemistry</subject><subject>Full Research Paper</subject><subject>general acid catalysis</subject><subject>gold catalysis</subject><subject>isotope effect</subject><subject>phosphine ligand effect</subject><subject>solvent effect</subject><issn>1860-5397</issn><issn>1860-5397</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVksFu1DAQQCMEoqVw4QNQjgU1y8R2HOdUoarASitxgbPl2JPUWydebKfS8hl8cZNuu2pPtsbPb2bsybKPJaxozcnXduv1isCK0VfZaSk4FBVt6tfP9ifZuxi3AAw48LfZCRWMQcnFafZ_Y3s1mhy7DnWKF3n07g7HlGvvdxhUsn68yBfCqdBjfmtHTFYfMYNTwmCnIbfRp_nKkym3Y957Z87XnwutknL7f2jmYApq8A71NPty5W5xxPxmb4JXgx0f0r3P3nTKRfzwuJ5lf75f_776WWx-_VhffdsUmgFLRYd1Q6qOCl6RhgtTEeR1BUILpVjDSmiYabFqm1J1ANgIU5q6VIIIijXtanqWrQ9e49VW7oIdVNhLr6x8CPjQSxXmXh1KYTiUujIUUMwP1wpCUGhdc63AEG1m1-XBtZvaAY3GpU_3QvryZLQ3svd3ci6znL8FZsP5oyH4vxPGJAcbNTqnRvRTlKShdQ2MUTqjXw6oDj7GgN0xTwlymQi5TIQkINkCf3pe2RF9GgF6D87WtZw</recordid><startdate>20240229</startdate><enddate>20240229</enddate><creator>Lan, Ruichen</creator><creator>Yager, Brock</creator><creator>Jee, Yoonsun</creator><creator>Day, Cynthia S</creator><creator>Jones, Amanda C</creator><general>Beilstein-Institut</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-7445-8311</orcidid><orcidid>https://orcid.org/0009-0008-9159-3791</orcidid></search><sort><creationdate>20240229</creationdate><title>Ligand effects, solvent cooperation, and large kinetic solvent deuterium isotope effects in gold(I)-catalyzed intramolecular alkene hydroamination</title><author>Lan, Ruichen ; Yager, Brock ; Jee, Yoonsun ; Day, Cynthia S ; Jones, Amanda C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-fe7925f38652968d52e67508c8aa4941094dbe5b91af00e98d1d71a8283e73f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>alkene hydroamination</topic><topic>Chemistry</topic><topic>Full Research Paper</topic><topic>general acid catalysis</topic><topic>gold catalysis</topic><topic>isotope effect</topic><topic>phosphine ligand effect</topic><topic>solvent effect</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lan, Ruichen</creatorcontrib><creatorcontrib>Yager, Brock</creatorcontrib><creatorcontrib>Jee, Yoonsun</creatorcontrib><creatorcontrib>Day, Cynthia S</creatorcontrib><creatorcontrib>Jones, Amanda C</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Beilstein journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lan, Ruichen</au><au>Yager, Brock</au><au>Jee, Yoonsun</au><au>Day, Cynthia S</au><au>Jones, Amanda C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ligand effects, solvent cooperation, and large kinetic solvent deuterium isotope effects in gold(I)-catalyzed intramolecular alkene hydroamination</atitle><jtitle>Beilstein journal of organic chemistry</jtitle><addtitle>Beilstein J Org Chem</addtitle><date>2024-02-29</date><risdate>2024</risdate><volume>20</volume><issue>1</issue><spage>479</spage><epage>496</epage><pages>479-496</pages><issn>1860-5397</issn><eissn>1860-5397</eissn><abstract>Kinetic studies on the intramolecular hydroamination of protected variants of 2,2-diphenylpent-4-en-1-amine were carried out under a variety of conditions with cationic gold catalysts supported by phosphine ligands. The impact of ligand on gold, protecting group on nitrogen, and solvent and additive on reaction rates was determined. The most effective reactions utilized more Lewis basic ureas, and more electron-withdrawing phosphines. A DCM/alcohol cooperative effect was quantified, and a continuum of isotope effects was measured with low KIE's in the absence of deuterated alcoholic solvent, increasing to large solvent KIE's when comparing reactions in pure MeOH to those in pure MeOH-
. The effects are interpreted both within the context of a classic gold π-activation/protodeauration mechanism and a general acid-catalyzed mechanism without intermediate gold alkyls.</abstract><cop>Germany</cop><pub>Beilstein-Institut</pub><pmid>38440168</pmid><doi>10.3762/bjoc.20.43</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0001-7445-8311</orcidid><orcidid>https://orcid.org/0009-0008-9159-3791</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1860-5397 |
ispartof | Beilstein journal of organic chemistry, 2024-02, Vol.20 (1), p.479-496 |
issn | 1860-5397 1860-5397 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_8d601c5d30e8401b822e8cc76ca0d2cd |
source | PubMed Central; ProQuest Publicly Available Content database |
subjects | alkene hydroamination Chemistry Full Research Paper general acid catalysis gold catalysis isotope effect phosphine ligand effect solvent effect |
title | Ligand effects, solvent cooperation, and large kinetic solvent deuterium isotope effects in gold(I)-catalyzed intramolecular alkene hydroamination |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T02%3A47%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ligand%20effects,%20solvent%20cooperation,%20and%20large%20kinetic%20solvent%20deuterium%20isotope%20effects%20in%20gold(I)-catalyzed%20intramolecular%20alkene%20hydroamination&rft.jtitle=Beilstein%20journal%20of%20organic%20chemistry&rft.au=Lan,%20Ruichen&rft.date=2024-02-29&rft.volume=20&rft.issue=1&rft.spage=479&rft.epage=496&rft.pages=479-496&rft.issn=1860-5397&rft.eissn=1860-5397&rft_id=info:doi/10.3762/bjoc.20.43&rft_dat=%3Cproquest_doaj_%3E2937704433%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c404t-fe7925f38652968d52e67508c8aa4941094dbe5b91af00e98d1d71a8283e73f73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2937704433&rft_id=info:pmid/38440168&rfr_iscdi=true |