About: Brønsted Acid Catalyzed, Conjugate Addition of β-Dicarbonyls to In Situ Generatedortho-Quinone Methides-Enantioselective Synthesis of 4-Aryl-4H-Chromenes

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About: Brønsted Acid Catalyzed, Conjugate Addition of β-Dicarbonyls to In Situ Generatedortho-Quinone Methides-Enantioselective Synthesis of 4-Aryl-4H-Chromenes Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) հոդված (hy) wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2014 (uk) article scientifique publié en 2014 (fr) im Juni 2014 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q64028693-06648816-858F-4962-B38F-E1901694BFC3
publication date	2014-06-18 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q64028693-7FC82B82-AE10-47B0-B9BF-453C6161EF16
language of work or name	English
cites work	wds:Q64028693-F149F9B4-78FA-4F81-935B-2051DF0B7EC8
cites work	New α-Glucosidase Inhibitors and Antibacterial Compounds fromMyrtus communis L.
author name string	wds:Q64028693-C0AB31D8-6EC9-444E-BD1A-88CB16ACBFE7 wds:Q64028693-F2321B0C-882F-4370-B5ED-481EA0E86787
author name string	Stefan Haseloff Santosh Kumar Alamsetti
rdfs:label	Brønsted Acid Catalyzed, Conjugate Addition of β-Dicarbonyls to In Situ Generatedortho-Quinone Methides-Enantioselective Synthesis of 4-Aryl-4H-Chromenes (en) Brønsted Acid Catalyzed, Conjugate Addition of β-Dicarbonyls to In Situ Generatedortho-Quinone Methides-Enantioselective Synthesis of 4-Aryl-4H-Chromenes (nl)
skos:prefLabel	Brønsted Acid Catalyzed, Conjugate Addition of β-Dicarbonyls to In Situ Generatedortho-Quinone Methides-Enantioselective Synthesis of 4-Aryl-4H-Chromenes (en) Brønsted Acid Catalyzed, Conjugate Addition of β-Dicarbonyls to In Situ Generatedortho-Quinone Methides-Enantioselective Synthesis of 4-Aryl-4H-Chromenes (nl)
name	Brønsted Acid Catalyzed, Conjugate Addition of β-Dicarbonyls to In Situ Generatedortho-Quinone Methides-Enantioselective Synthesis of 4-Aryl-4H-Chromenes (en) Brønsted Acid Catalyzed, Conjugate Addition of β-Dicarbonyls to In Situ Generatedortho-Quinone Methides-Enantioselective Synthesis of 4-Aryl-4H-Chromenes (nl)
author	wds:Q64028693-661E2A37-3678-4B3F-92F1-8481AF40C172 wds:Q64028693-6DE1F4A2-4CE2-4E5C-B069-5232EA0742F5
author	Christoph Schneider Osama El-Sepelgy
title	wds:Q64028693-D77D0C64-6BD7-404A-9F65-188D8B3DC40F
title	Brønsted acid catalyzed, conjugate addition of β-dicarbonyls to in situ generated ortho-quinone methides--enantioselective synthesis of 4-aryl-4H-chromenes (en)
page(s)	wds:Q64028693-576F60F4-190C-4CA5-AA24-113E22674ADC
page(s)	7923-7927
instance of	wds:Q64028693-9FF4F159-1A69-4EB7-BED7-9538E53FEAE4
instance of	scholarly article
main subject	wds:Q64028693-5E708228-E32E-44B1-911C-2EF40D34DD4E
main subject	enantioselectivity
PubMed ID	wds:Q64028693-9184ECD9-824C-4337-91CC-3079E53A5B30
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/24938645
PubMed ID	24938645
published in	wds:Q64028693-EF1DF1FC-BFFB-4FE4-9255-CB70E68ED4C9
published in	Angewandte Chemie International Edition
issue	wds:Q64028693-510E8408-DDE0-4D83-82E1-FACA47EB1E0E
volume	wds:Q64028693-F58D6143-1DF5-4721-A360-60DC61A4E38A
issue	30
volume	53
DOI	wds:Q64028693-D20E9D43-501D-40EF-B373-8C883460C5A1
DOI	http://dx.doi.org/10.1002/ANIE.201403573
DOI	10.1002/ANIE.201403573
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q64028693
is cites work of	The Emergence of Quinone Methides in Asymmetric Organocatalysis Thiourea-catalyzed enantioselective addition of indoles to pyrones: alkaloid cores with quaternary carbons Michael Additions of Highly Basic Enolates to ortho-Quinone Methides The organocatalytic asymmetric Prins cyclization Ferrocene-Decorated Phenol Derivatives by Trapping ortho -Quinone Methide Intermediates with Ferrocene Redox-triggered cascade dearomative cyclizations enabled by hexafluoroisopropanol Enantioselective Multicomponent Condensation Reactions of Phenols, Aldehydes, and Boronates Catalyzed by Chiral Biphenols Catalytic Asymmetric Intramolecular [4+2] Cycloaddition of In Situ Generated ortho-Quinone Methides. Multicomponent Condensation Reactions via ortho-Quinone Methides. Evolution of a Strategy for the Enantioselective Total Synthesis of (+)-Psiguadial B Cooperative Catalysis for the Highly Diastereo- and Enantioselective [4+3]-Cycloannulation of ortho-Quinone Methides and Carbonyl Ylides Divergent Total Syntheses of Rhodomyrtosones A and B.
is cites work of	wds:Q28082249-5CDC1D37-0B37-4A74-94C4-1A6363461310 wds:Q35846906-FC433EFD-C13A-44B9-B5AB-2C07F7849E2F wds:Q43141595-05BBBE2F-F7AB-4FFC-897F-03636B58DEF0 wds:Q62029813-84381E23-F914-4617-9FEF-6F0FDE1777AC wds:Q50666506-2DD8D121-8348-4C58-A855-AD6D3BCA27D8 wds:Q34531447-CBE57BA8-AC88-4036-B278-49E7B53A8607 wds:Q60106500-A7CDEBD3-5655-4E82-A3DA-32EF19402641 wds:Q90442481-86D5AB14-1C93-4699-9C6C-75D7AD3A86BE wds:Q92373487-DF0F513A-EC0D-4B99-B21C-7671E25F604B wds:Q48224062-542CC59D-93FB-48ED-BC4F-AFE5D538B5CE wds:Q85220191-27614E23-2AB6-4348-A239-545548340286 wds:Q36276156-6D7DE966-C2F3-4A81-ABC9-7E79ED1ECF68

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