ChemInform Abstract: Uniting C1‐Ammonium Enolates and Transition Metal Electrophiles via Cooperative Catalysis: The Direct Asymmetric α‐Allylation of Aryl Acetic Acid Esters. Issue 40 (September 2016)

Record Type:
Journal Article
Title:
ChemInform Abstract: Uniting C1‐Ammonium Enolates and Transition Metal Electrophiles via Cooperative Catalysis: The Direct Asymmetric α‐Allylation of Aryl Acetic Acid Esters. Issue 40 (September 2016)
Main Title:
ChemInform Abstract: Uniting C1‐Ammonium Enolates and Transition Metal Electrophiles via Cooperative Catalysis: The Direct Asymmetric α‐Allylation of Aryl Acetic Acid Esters.
Authors:
Schwarz, Kevin J.
Amos, Jessica L.
Klein, J. Cullen
Do, Dung T.
Snaddon, Thomas N.
Abstract:
Abstract: Allylmethane sulfonate as well as diverse aryl substituted allyl carbonates efficiently react with pentafluorophenyl 2‐arylacetates to form α‐allylated products in high yields and with very high enantiomeric excesses.
Is Part Of:
ChemInform. Volume 47:Issue 40(2016)
Journal:
ChemInform
Issue:
Volume 47:Issue 40(2016)
Issue Display:
Volume 47, Issue 40 (2016)
Year:
2016
Volume:
47
Issue:
40
Issue Sort Value:
2016-0047-0040-0000
Page Start:
no
Page End:
no
Publication Date:
2016-09
Subjects:
halogen compounds (benzene compounds) -- carboxylic acid esters (benzene compounds) -- C‐C bond formation -- diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) -- catalysis, phase‐transfer catalysis
Chemistry -- Abstracts -- Periodicals
540.5
Journal URLs:
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1522-2667 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:
10.1002/chin.201640069 ↗
Languages:
English
ISSNs:
0931-7597
Deposit Type:
Legaldeposit
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:
British Library DSC - 3158.195000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:
2380.xml