About: Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: efficient synthesis of chiral γ-amino acid derivatives

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About: Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: efficient synthesis of chiral γ-amino acid derivatives Goto Sponge NotDistinct Permalink

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scientific article published on 15 September 2011

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 2011 (uk) article scientifique publié en 2011 (fr) scientific article published on 15 September 2011 (en) artículu científicu espublizáu en setiembre de 2011 (ast)
publication date	wds:Q84915201-8E95657A-8DA2-46C9-85C6-08BC4949FA0A
publication date	2011-09-15 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q84915201-85D3C4C5-770D-40F0-8735-838C84F93979
language of work or name	English
author name string	wds:Q84915201-71CE0BAA-AA66-4BBD-965E-E0AB56FDB360 wds:Q84915201-AD0938CB-5CA6-460A-A624-C38942765525 wds:Q84915201-F200B205-C702-457E-9537-C05C5041C146
author name string	Song Ye Li-Tao Shen Li-Hui Sun
rdfs:label	Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: efficient synthesis of chiral γ-amino acid derivatives (en) Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: efficient synthesis of chiral γ-amino acid derivatives (nl)
skos:prefLabel	Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: efficient synthesis of chiral γ-amino acid derivatives (en) Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: efficient synthesis of chiral γ-amino acid derivatives (nl)
name	Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: efficient synthesis of chiral γ-amino acid derivatives (en) Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: efficient synthesis of chiral γ-amino acid derivatives (nl)
title	wds:Q84915201-3E70781D-274C-4BBA-A583-6A63670637DF
title	Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: efficient synthesis of chiral γ-amino acid derivatives (en)
page(s)	wds:Q84915201-0D418466-7CD2-4ECE-AB56-33426E1914E1
page(s)	15894-15897
instance of	wds:Q84915201-E4A76548-C81F-4241-AEE0-BDC106B00C73
instance of	scholarly article
main subject	wds:Q84915201-9D504DAD-014D-4886-933C-FC68EC990FCD wds:Q84915201-CF6E657A-5F70-4918-8BD8-8CE77FBD7A71
main subject	chirality enantioselectivity
PubMed ID	wds:Q84915201-99D54AB3-8286-4203-B1CE-F226646A11EF
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/21902208
PubMed ID	21902208
published in	wds:Q84915201-93266211-A96D-4900-AEC4-EB6BB20D4930
published in	Journal of the American Chemical Society
issue	wds:Q84915201-30B6E433-C974-4FC9-8AF4-A8FE3A36A5EC
volume	wds:Q84915201-198A4A2A-3C6A-409D-A282-17C9A5B4685E
issue	40
volume	133
DOI	wds:Q84915201-FEC279C9-CB3E-436F-BD01-DC35EF61FBA8
DOI	http://dx.doi.org/10.1021/JA206819Y
DOI	10.1021/JA206819Y
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q84915201
is cites work of	Synthesis of tetrahydropyridazines by a metal-carbene-directed enantioselective vinylogous N-H insertion/Lewis acid-catalyzed diastereoselective Mannich addition. Cycloaddition of cyclobutenone and azomethine imine enabled by chiral isothiourea organic catalysts. Carbon-carbon bond activation of cyclobutenones enabled by the addition of chiral organocatalyst to ketone Catalytic Asymmetric Synthesis of Trifluoromethylated γ-Amino Acids through the Umpolung Addition of Trifluoromethyl Imines to Carboxylic Acid Derivatives. Direct Catalytic Asymmetric Synthesis of Trifluoromethylated γ-Amino Esters/Lactones via Umpolung Strategy Asymmetric Organocatalysis: The Emerging Utility of α,β-Unsaturated Acylammonium Salts.
is cites work of	wds:Q48133101-1D0C39D5-A50F-4456-A998-5DE285C8CA88 wds:Q35081968-18A608AE-A6FE-40A5-AA62-AE266C922C7D wds:Q90449778-F265E459-EE76-4AB1-B634-0F8BA4CBEF60 wds:Q36138930-A6B70860-FDBD-446D-8A05-C50AE8CE11D3 wds:Q49870526-CCF658FE-0989-4E17-BFDF-019F2E402268 wds:Q36452754-CB289ABA-E898-4CEE-9C08-1FBF8AFA346C

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