Loading…
Ni-Catalyzed Enantioselective Conjunctive Cross-Coupling of 9-BBN Borates
Catalytic enantioselective conjunctive cross-coupling between 9-BBN borate complexes and aryl electrophiles can be accomplished with Ni salts in the presence of a chiral diamine ligand. The reactions furnish chiral 9-BBN derivatives in an enantioselective fashion and these are converted to chiral al...
Saved in:
Published in: | Angewandte Chemie International Edition 2017-08, Vol.56 (39), p.11870-11874 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 11874 |
container_issue | 39 |
container_start_page | 11870 |
container_title | Angewandte Chemie International Edition |
container_volume | 56 |
creator | Chierchia, Matteo Law, Chunyin Morken, James P. |
description | Catalytic enantioselective conjunctive cross-coupling between 9-BBN borate complexes and aryl electrophiles can be accomplished with Ni salts in the presence of a chiral diamine ligand. The reactions furnish chiral 9-BBN derivatives in an enantioselective fashion and these are converted to chiral alcohols and amines, or engaged in other stereospecific C-C bond forming reactions.
Conjunctive Coupling
: Ni-Catalyzed conjunctive couplings furnish chiral 9-BBN derivatives in an enantioselective fashion and these are converted to chiral alcohols and amines, or they can be engaged in other stereospecific C-C bond forming reactions. |
doi_str_mv | 10.1002/anie.201706719 |
format | article |
fullrecord | <record><control><sourceid>pubmedcentral</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5699474</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_5699474</sourcerecordid><originalsourceid>FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_56994743</originalsourceid><addsrcrecordid>eNqljLtOAzEUBS0EIuHRUvsHHPza9bqh2FVQaFLRW5fkJjhy7JXtjRS-nhRpqKlmpDk6hLwIvhCcy1eIHheSC8NbI-wNmYtGCqaMUbcX10ox0zViRh5KOVz2XcfbezKTndHSaj0nH2vPBqgQzj-4pcsIsfpUMOCm-hPSIcXDFK-eUylsSNMYfNzTtKOW9f2a9ilDxfJE7nYQCj5f-Uje3pefw4qN09cRtxuMNUNwY_ZHyGeXwLu_Jfpvt08n17TWaqPVvw9-ATDMW10</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Ni-Catalyzed Enantioselective Conjunctive Cross-Coupling of 9-BBN Borates</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Chierchia, Matteo ; Law, Chunyin ; Morken, James P.</creator><creatorcontrib>Chierchia, Matteo ; Law, Chunyin ; Morken, James P.</creatorcontrib><description>Catalytic enantioselective conjunctive cross-coupling between 9-BBN borate complexes and aryl electrophiles can be accomplished with Ni salts in the presence of a chiral diamine ligand. The reactions furnish chiral 9-BBN derivatives in an enantioselective fashion and these are converted to chiral alcohols and amines, or engaged in other stereospecific C-C bond forming reactions.
Conjunctive Coupling
: Ni-Catalyzed conjunctive couplings furnish chiral 9-BBN derivatives in an enantioselective fashion and these are converted to chiral alcohols and amines, or they can be engaged in other stereospecific C-C bond forming reactions.</description><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201706719</identifier><identifier>PMID: 28742944</identifier><language>eng</language><ispartof>Angewandte Chemie International Edition, 2017-08, Vol.56 (39), p.11870-11874</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids></links><search><creatorcontrib>Chierchia, Matteo</creatorcontrib><creatorcontrib>Law, Chunyin</creatorcontrib><creatorcontrib>Morken, James P.</creatorcontrib><title>Ni-Catalyzed Enantioselective Conjunctive Cross-Coupling of 9-BBN Borates</title><title>Angewandte Chemie International Edition</title><description>Catalytic enantioselective conjunctive cross-coupling between 9-BBN borate complexes and aryl electrophiles can be accomplished with Ni salts in the presence of a chiral diamine ligand. The reactions furnish chiral 9-BBN derivatives in an enantioselective fashion and these are converted to chiral alcohols and amines, or engaged in other stereospecific C-C bond forming reactions.
Conjunctive Coupling
: Ni-Catalyzed conjunctive couplings furnish chiral 9-BBN derivatives in an enantioselective fashion and these are converted to chiral alcohols and amines, or they can be engaged in other stereospecific C-C bond forming reactions.</description><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqljLtOAzEUBS0EIuHRUvsHHPza9bqh2FVQaFLRW5fkJjhy7JXtjRS-nhRpqKlmpDk6hLwIvhCcy1eIHheSC8NbI-wNmYtGCqaMUbcX10ox0zViRh5KOVz2XcfbezKTndHSaj0nH2vPBqgQzj-4pcsIsfpUMOCm-hPSIcXDFK-eUylsSNMYfNzTtKOW9f2a9ilDxfJE7nYQCj5f-Uje3pefw4qN09cRtxuMNUNwY_ZHyGeXwLu_Jfpvt08n17TWaqPVvw9-ATDMW10</recordid><startdate>20170817</startdate><enddate>20170817</enddate><creator>Chierchia, Matteo</creator><creator>Law, Chunyin</creator><creator>Morken, James P.</creator><scope>5PM</scope></search><sort><creationdate>20170817</creationdate><title>Ni-Catalyzed Enantioselective Conjunctive Cross-Coupling of 9-BBN Borates</title><author>Chierchia, Matteo ; Law, Chunyin ; Morken, James P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_56994743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chierchia, Matteo</creatorcontrib><creatorcontrib>Law, Chunyin</creatorcontrib><creatorcontrib>Morken, James P.</creatorcontrib><collection>PubMed Central (Full Participant titles)</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chierchia, Matteo</au><au>Law, Chunyin</au><au>Morken, James P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ni-Catalyzed Enantioselective Conjunctive Cross-Coupling of 9-BBN Borates</atitle><jtitle>Angewandte Chemie International Edition</jtitle><date>2017-08-17</date><risdate>2017</risdate><volume>56</volume><issue>39</issue><spage>11870</spage><epage>11874</epage><pages>11870-11874</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>Catalytic enantioselective conjunctive cross-coupling between 9-BBN borate complexes and aryl electrophiles can be accomplished with Ni salts in the presence of a chiral diamine ligand. The reactions furnish chiral 9-BBN derivatives in an enantioselective fashion and these are converted to chiral alcohols and amines, or engaged in other stereospecific C-C bond forming reactions.
Conjunctive Coupling
: Ni-Catalyzed conjunctive couplings furnish chiral 9-BBN derivatives in an enantioselective fashion and these are converted to chiral alcohols and amines, or they can be engaged in other stereospecific C-C bond forming reactions.</abstract><pmid>28742944</pmid><doi>10.1002/anie.201706719</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1433-7851 |
ispartof | Angewandte Chemie International Edition, 2017-08, Vol.56 (39), p.11870-11874 |
issn | 1433-7851 1521-3773 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5699474 |
source | Wiley-Blackwell Read & Publish Collection |
title | Ni-Catalyzed Enantioselective Conjunctive Cross-Coupling of 9-BBN Borates |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T13%3A08%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmedcentral&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ni-Catalyzed%20Enantioselective%20Conjunctive%20Cross-Coupling%20of%209-BBN%20Borates&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Chierchia,%20Matteo&rft.date=2017-08-17&rft.volume=56&rft.issue=39&rft.spage=11870&rft.epage=11874&rft.pages=11870-11874&rft.issn=1433-7851&rft.eissn=1521-3773&rft_id=info:doi/10.1002/anie.201706719&rft_dat=%3Cpubmedcentral%3Epubmedcentral_primary_oai_pubmedcentral_nih_gov_5699474%3C/pubmedcentral%3E%3Cgrp_id%3Ecdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_56994743%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/28742944&rfr_iscdi=true |