Loading…

Highly enantioselective conjugate addition of aldehydes to nitroolefins catalyzed by chiral bifunctional sulfamides

Chiral bifunctional sulfamides were found to be highly efficient organocatalysts for the conjugate addition of aldehydes to nitroolefins in the presence of base additives.

Saved in:

Bibliographic Details
Published in:	Chemical communications (Cambridge, England) England), 2009-01 (7), p.833-835
Main Authors:	Zhang, Xue-Jing, Liu, Sheng-Ping, Li, Xue-Ming, Yan, Ming, Chan, Albert S C
Format:	Article
Language:	English
Subjects:	Aldehydes - chemistry Alkenes - chemistry Amines - chemistry Catalysis Cross-Linking Reagents - chemical synthesis Cross-Linking Reagents - chemistry Stereoisomerism Substrate Specificity Sulfonamides - chemistry
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-c347t-cf81ed8720ac7f5f37f11fde21bd8f251db28fbfab83902135460061d17e4b53
cites	cdi_FETCH-LOGICAL-c347t-cf81ed8720ac7f5f37f11fde21bd8f251db28fbfab83902135460061d17e4b53
container_end_page	835
container_issue	7
container_start_page	833
container_title	Chemical communications (Cambridge, England)
container_volume
creator	Zhang, Xue-Jing Liu, Sheng-Ping Li, Xue-Ming Yan, Ming Chan, Albert S C
description	Chiral bifunctional sulfamides were found to be highly efficient organocatalysts for the conjugate addition of aldehydes to nitroolefins in the presence of base additives.
doi_str_mv	10.1039/b818582d
format	article
fullrecord	<record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67072739</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67072739</sourcerecordid><originalsourceid>FETCH-LOGICAL-c347t-cf81ed8720ac7f5f37f11fde21bd8f251db28fbfab83902135460061d17e4b53</originalsourceid><addsrcrecordid>eNpFkMtLxDAQxoMori_wL5CcxEs1j6ZJj75XELx48FbymOxmyTZr0wr1r7fLLjiXmWF-3wfzIXRJyS0lvL4ziiqhmDtAJ5RXZSFK9XW4nUVdSF6KGTrNeUWmokIdoxmtOWOlkCcoz8NiGUcMrW77kDJEsH34AWxTuxoWugesnQvTqcXJYx0dLEcHGfcJt6HvUorgQ5ux1b2O4y84bEZsl6HTEZvgh9ZutdOSh-j1Okzac3Tkdcxwse9n6PPl-fNxXrx_vL493r8XlpeyL6xXFJySjGgrvfBcekq9A0aNU54J6gxT3nhtFK8Jm54tK0Iq6qiE0gh-hq53tpsufQ-Q-2YdsoUYdQtpyE0liWSS1xN4swNtl3LuwDebLqx1NzaUNNt8m4ddvk8TerX3HMwa3D-4D5T_AdgteHU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67072739</pqid></control><display><type>article</type><title>Highly enantioselective conjugate addition of aldehydes to nitroolefins catalyzed by chiral bifunctional sulfamides</title><source>Royal Society of Chemistry</source><creator>Zhang, Xue-Jing ; Liu, Sheng-Ping ; Li, Xue-Ming ; Yan, Ming ; Chan, Albert S C</creator><creatorcontrib>Zhang, Xue-Jing ; Liu, Sheng-Ping ; Li, Xue-Ming ; Yan, Ming ; Chan, Albert S C</creatorcontrib><description>Chiral bifunctional sulfamides were found to be highly efficient organocatalysts for the conjugate addition of aldehydes to nitroolefins in the presence of base additives.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/b818582d</identifier><identifier>PMID: 19322457</identifier><language>eng</language><publisher>England</publisher><subject>Aldehydes - chemistry ; Alkenes - chemistry ; Amines - chemistry ; Catalysis ; Cross-Linking Reagents - chemical synthesis ; Cross-Linking Reagents - chemistry ; Stereoisomerism ; Substrate Specificity ; Sulfonamides - chemistry</subject><ispartof>Chemical communications (Cambridge, England), 2009-01 (7), p.833-835</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c347t-cf81ed8720ac7f5f37f11fde21bd8f251db28fbfab83902135460061d17e4b53</citedby><cites>FETCH-LOGICAL-c347t-cf81ed8720ac7f5f37f11fde21bd8f251db28fbfab83902135460061d17e4b53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19322457$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Xue-Jing</creatorcontrib><creatorcontrib>Liu, Sheng-Ping</creatorcontrib><creatorcontrib>Li, Xue-Ming</creatorcontrib><creatorcontrib>Yan, Ming</creatorcontrib><creatorcontrib>Chan, Albert S C</creatorcontrib><title>Highly enantioselective conjugate addition of aldehydes to nitroolefins catalyzed by chiral bifunctional sulfamides</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>Chiral bifunctional sulfamides were found to be highly efficient organocatalysts for the conjugate addition of aldehydes to nitroolefins in the presence of base additives.</description><subject>Aldehydes - chemistry</subject><subject>Alkenes - chemistry</subject><subject>Amines - chemistry</subject><subject>Catalysis</subject><subject>Cross-Linking Reagents - chemical synthesis</subject><subject>Cross-Linking Reagents - chemistry</subject><subject>Stereoisomerism</subject><subject>Substrate Specificity</subject><subject>Sulfonamides - chemistry</subject><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNpFkMtLxDAQxoMori_wL5CcxEs1j6ZJj75XELx48FbymOxmyTZr0wr1r7fLLjiXmWF-3wfzIXRJyS0lvL4ziiqhmDtAJ5RXZSFK9XW4nUVdSF6KGTrNeUWmokIdoxmtOWOlkCcoz8NiGUcMrW77kDJEsH34AWxTuxoWugesnQvTqcXJYx0dLEcHGfcJt6HvUorgQ5ux1b2O4y84bEZsl6HTEZvgh9ZutdOSh-j1Okzac3Tkdcxwse9n6PPl-fNxXrx_vL493r8XlpeyL6xXFJySjGgrvfBcekq9A0aNU54J6gxT3nhtFK8Jm54tK0Iq6qiE0gh-hq53tpsufQ-Q-2YdsoUYdQtpyE0liWSS1xN4swNtl3LuwDebLqx1NzaUNNt8m4ddvk8TerX3HMwa3D-4D5T_AdgteHU</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Zhang, Xue-Jing</creator><creator>Liu, Sheng-Ping</creator><creator>Li, Xue-Ming</creator><creator>Yan, Ming</creator><creator>Chan, Albert S C</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090101</creationdate><title>Highly enantioselective conjugate addition of aldehydes to nitroolefins catalyzed by chiral bifunctional sulfamides</title><author>Zhang, Xue-Jing ; Liu, Sheng-Ping ; Li, Xue-Ming ; Yan, Ming ; Chan, Albert S C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c347t-cf81ed8720ac7f5f37f11fde21bd8f251db28fbfab83902135460061d17e4b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aldehydes - chemistry</topic><topic>Alkenes - chemistry</topic><topic>Amines - chemistry</topic><topic>Catalysis</topic><topic>Cross-Linking Reagents - chemical synthesis</topic><topic>Cross-Linking Reagents - chemistry</topic><topic>Stereoisomerism</topic><topic>Substrate Specificity</topic><topic>Sulfonamides - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Xue-Jing</creatorcontrib><creatorcontrib>Liu, Sheng-Ping</creatorcontrib><creatorcontrib>Li, Xue-Ming</creatorcontrib><creatorcontrib>Yan, Ming</creatorcontrib><creatorcontrib>Chan, Albert S C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Xue-Jing</au><au>Liu, Sheng-Ping</au><au>Li, Xue-Ming</au><au>Yan, Ming</au><au>Chan, Albert S C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly enantioselective conjugate addition of aldehydes to nitroolefins catalyzed by chiral bifunctional sulfamides</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2009-01-01</date><risdate>2009</risdate><issue>7</issue><spage>833</spage><epage>835</epage><pages>833-835</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>Chiral bifunctional sulfamides were found to be highly efficient organocatalysts for the conjugate addition of aldehydes to nitroolefins in the presence of base additives.</abstract><cop>England</cop><pmid>19322457</pmid><doi>10.1039/b818582d</doi><tpages>3</tpages></addata></record>
fulltext	fulltext
identifier	ISSN: 1359-7345
ispartof	Chemical communications (Cambridge, England), 2009-01 (7), p.833-835
issn	1359-7345 1364-548X
language	eng
recordid	cdi_proquest_miscellaneous_67072739
source	Royal Society of Chemistry
subjects	Aldehydes - chemistry Alkenes - chemistry Amines - chemistry Catalysis Cross-Linking Reagents - chemical synthesis Cross-Linking Reagents - chemistry Stereoisomerism Substrate Specificity Sulfonamides - chemistry
title	Highly enantioselective conjugate addition of aldehydes to nitroolefins catalyzed by chiral bifunctional sulfamides
url	http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T22%3A59%3A43IST&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=Highly%20enantioselective%20conjugate%20addition%20of%20aldehydes%20to%20nitroolefins%20catalyzed%20by%20chiral%20bifunctional%20sulfamides&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=Zhang,%20Xue-Jing&rft.date=2009-01-01&rft.issue=7&rft.spage=833&rft.epage=835&rft.pages=833-835&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/b818582d&rft_dat=%3Cproquest_cross%3E67072739%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c347t-cf81ed8720ac7f5f37f11fde21bd8f251db28fbfab83902135460061d17e4b53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=67072739&rft_id=info:pmid/19322457&rfr_iscdi=true