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Recent Developments in Asymmetric Catalysis in the Presence of Chiral Gold Complexes
Abstract Catalytic asymmetric gold-catalyzed reactions provide versatile routes to enantiomerically enriched carbo- and heterocycles. This review summarizes the recent work on the development of novel catalytic systems combining gold and a chiral ligand. 1 Introduction 2 Gold-Catalyzed Activation of...
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Published in: | Synthesis (Stuttgart) 2011-05, Vol.2011 (10), p.1501-1514 |
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container_end_page | 1514 |
container_issue | 10 |
container_start_page | 1501 |
container_title | Synthesis (Stuttgart) |
container_volume | 2011 |
creator | Pradal, Alexandre Toullec, Patrick Y. Michelet, Véronique |
description | Abstract
Catalytic asymmetric gold-catalyzed reactions provide versatile
routes to enantiomerically enriched carbo- and heterocycles. This
review summarizes the recent work on the development of novel catalytic
systems combining gold and a chiral ligand.
1 Introduction
2 Gold-Catalyzed Activation of Carbonyl and Imine-Type Bonds
3 Gold-Catalyzed Activation of Alkenes
3.1 Hydrogenation Reactions
3.2 Nucleophilic Additions to Alkenes
4 Gold-Catalyzed Activation of Allenes
4.1 In the Presence of a Chiral Gold Complex
4.1.1 Oxygen Nucleophiles
4.1.2 Nitrogen Nucleophiles
4.1.3 Carbon Nucleophiles
4.2 In the Presence of a Chiral Silver Salt
5 Gold-Catalyzed Activation of Alkynes
5.1 Rearrangement of Propargylic Esters
5.2 Desymmetrization Reactions
5.3 Cycloisomerization of Enynes
5.3.1 In the Absence of an External Nucleophile
5.3.2 In the Presence of a Nucleophile: Domino Processes
5.3.2.1 Oxygen and Nitrogen Nucleophiles
5.3.2.2 Carbon Nucleophiles
6 Conclusion |
doi_str_mv | 10.1055/s-0030-1258465 |
format | article |
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Catalytic asymmetric gold-catalyzed reactions provide versatile
routes to enantiomerically enriched carbo- and heterocycles. This
review summarizes the recent work on the development of novel catalytic
systems combining gold and a chiral ligand.
1 Introduction
2 Gold-Catalyzed Activation of Carbonyl and Imine-Type Bonds
3 Gold-Catalyzed Activation of Alkenes
3.1 Hydrogenation Reactions
3.2 Nucleophilic Additions to Alkenes
4 Gold-Catalyzed Activation of Allenes
4.1 In the Presence of a Chiral Gold Complex
4.1.1 Oxygen Nucleophiles
4.1.2 Nitrogen Nucleophiles
4.1.3 Carbon Nucleophiles
4.2 In the Presence of a Chiral Silver Salt
5 Gold-Catalyzed Activation of Alkynes
5.1 Rearrangement of Propargylic Esters
5.2 Desymmetrization Reactions
5.3 Cycloisomerization of Enynes
5.3.1 In the Absence of an External Nucleophile
5.3.2 In the Presence of a Nucleophile: Domino Processes
5.3.2.1 Oxygen and Nitrogen Nucleophiles
5.3.2.2 Carbon Nucleophiles
6 Conclusion</description><identifier>ISSN: 0039-7881</identifier><identifier>EISSN: 1437-210X</identifier><identifier>DOI: 10.1055/s-0030-1258465</identifier><identifier>CODEN: SYNTBF</identifier><language>eng</language><publisher>Stuttgart: Thieme</publisher><subject>Catalysis ; Catalysts: preparations and properties ; Chemistry ; Exact sciences and technology ; General and physical chemistry ; Kinetics and mechanisms ; Organic chemistry ; Reactivity and mechanisms ; review ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>Synthesis (Stuttgart), 2011-05, Vol.2011 (10), p.1501-1514</ispartof><rights>Georg Thieme Verlag Stuttgart ˙ New York</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c307t-ed8a31d6319fefb6c130cf81f8c50603d70a39e95a376a347fb2ba9af3ae17e83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0030-1258465.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-0030-1258465$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,780,784,3017,3018,27924,27925,54559,54560</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24142379$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Pradal, Alexandre</creatorcontrib><creatorcontrib>Toullec, Patrick Y.</creatorcontrib><creatorcontrib>Michelet, Véronique</creatorcontrib><title>Recent Developments in Asymmetric Catalysis in the Presence of Chiral Gold Complexes</title><title>Synthesis (Stuttgart)</title><addtitle>Synthesis</addtitle><description>Abstract
Catalytic asymmetric gold-catalyzed reactions provide versatile
routes to enantiomerically enriched carbo- and heterocycles. This
review summarizes the recent work on the development of novel catalytic
systems combining gold and a chiral ligand.
1 Introduction
2 Gold-Catalyzed Activation of Carbonyl and Imine-Type Bonds
3 Gold-Catalyzed Activation of Alkenes
3.1 Hydrogenation Reactions
3.2 Nucleophilic Additions to Alkenes
4 Gold-Catalyzed Activation of Allenes
4.1 In the Presence of a Chiral Gold Complex
4.1.1 Oxygen Nucleophiles
4.1.2 Nitrogen Nucleophiles
4.1.3 Carbon Nucleophiles
4.2 In the Presence of a Chiral Silver Salt
5 Gold-Catalyzed Activation of Alkynes
5.1 Rearrangement of Propargylic Esters
5.2 Desymmetrization Reactions
5.3 Cycloisomerization of Enynes
5.3.1 In the Absence of an External Nucleophile
5.3.2 In the Presence of a Nucleophile: Domino Processes
5.3.2.1 Oxygen and Nitrogen Nucleophiles
5.3.2.2 Carbon Nucleophiles
6 Conclusion</description><subject>Catalysis</subject><subject>Catalysts: preparations and properties</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Kinetics and mechanisms</subject><subject>Organic chemistry</subject><subject>Reactivity and mechanisms</subject><subject>review</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><issn>0039-7881</issn><issn>1437-210X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp1kM1Lw0AQxRdRsFavnvficetsNskmxxK1CgVFKngL080sTdl8sBvF_vdNbfHmaYaZ93vwHmO3EmYSkuQ-CAAFQkZJFqfJGZvIWGkRSfg8Z5PxlQudZfKSXYWwBQAdqXzCVu9kqB34A32T6_pm3AOvWz4Pu6ahwdeGFzig24X69z5siL95CtQa4p3lxab26PiicxUvuqZ39EPhml1YdIFuTnPKPp4eV8WzWL4uXor5UhgFehBUZahklSqZW7Lr1EgFxmbSZiaBFFSlAVVOeYJKp6hibdfRGnO0CklqytSUzY6-xncheLJl7-sG_a6UUB46KUN56KQ8dTICd0egx2DQWY-tqcMfFcUyjpTOR5046oZNTQ2V2-7Lt2OS_3z3hflv-g</recordid><startdate>20110501</startdate><enddate>20110501</enddate><creator>Pradal, Alexandre</creator><creator>Toullec, Patrick Y.</creator><creator>Michelet, Véronique</creator><general>Thieme</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20110501</creationdate><title>Recent Developments in Asymmetric Catalysis in the Presence of Chiral Gold Complexes</title><author>Pradal, Alexandre ; Toullec, Patrick Y. ; Michelet, Véronique</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c307t-ed8a31d6319fefb6c130cf81f8c50603d70a39e95a376a347fb2ba9af3ae17e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Catalysis</topic><topic>Catalysts: preparations and properties</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Kinetics and mechanisms</topic><topic>Organic chemistry</topic><topic>Reactivity and mechanisms</topic><topic>review</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pradal, Alexandre</creatorcontrib><creatorcontrib>Toullec, Patrick Y.</creatorcontrib><creatorcontrib>Michelet, Véronique</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Synthesis (Stuttgart)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pradal, Alexandre</au><au>Toullec, Patrick Y.</au><au>Michelet, Véronique</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recent Developments in Asymmetric Catalysis in the Presence of Chiral Gold Complexes</atitle><jtitle>Synthesis (Stuttgart)</jtitle><addtitle>Synthesis</addtitle><date>2011-05-01</date><risdate>2011</risdate><volume>2011</volume><issue>10</issue><spage>1501</spage><epage>1514</epage><pages>1501-1514</pages><issn>0039-7881</issn><eissn>1437-210X</eissn><coden>SYNTBF</coden><abstract>Abstract
Catalytic asymmetric gold-catalyzed reactions provide versatile
routes to enantiomerically enriched carbo- and heterocycles. This
review summarizes the recent work on the development of novel catalytic
systems combining gold and a chiral ligand.
1 Introduction
2 Gold-Catalyzed Activation of Carbonyl and Imine-Type Bonds
3 Gold-Catalyzed Activation of Alkenes
3.1 Hydrogenation Reactions
3.2 Nucleophilic Additions to Alkenes
4 Gold-Catalyzed Activation of Allenes
4.1 In the Presence of a Chiral Gold Complex
4.1.1 Oxygen Nucleophiles
4.1.2 Nitrogen Nucleophiles
4.1.3 Carbon Nucleophiles
4.2 In the Presence of a Chiral Silver Salt
5 Gold-Catalyzed Activation of Alkynes
5.1 Rearrangement of Propargylic Esters
5.2 Desymmetrization Reactions
5.3 Cycloisomerization of Enynes
5.3.1 In the Absence of an External Nucleophile
5.3.2 In the Presence of a Nucleophile: Domino Processes
5.3.2.1 Oxygen and Nitrogen Nucleophiles
5.3.2.2 Carbon Nucleophiles
6 Conclusion</abstract><cop>Stuttgart</cop><pub>Thieme</pub><doi>10.1055/s-0030-1258465</doi><tpages>14</tpages></addata></record> |
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subjects | Catalysis Catalysts: preparations and properties Chemistry Exact sciences and technology General and physical chemistry Kinetics and mechanisms Organic chemistry Reactivity and mechanisms review Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Recent Developments in Asymmetric Catalysis in the Presence of Chiral Gold Complexes |
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