ChemInform Abstract: Unique Features of Chiral Palladium Enolates Derived from β‐Ketoamide: Structure and Catalytic Asymmetric Michael and Fluorination Reactions. Issue 50 (December 2015)

Record Type:: Journal Article
Title:: ChemInform Abstract: Unique Features of Chiral Palladium Enolates Derived from β‐Ketoamide: Structure and Catalytic Asymmetric Michael and Fluorination Reactions. Issue 50 (December 2015)
Main Title:: ChemInform Abstract: Unique Features of Chiral Palladium Enolates Derived from β‐Ketoamide: Structure and Catalytic Asymmetric Michael and Fluorination Reactions.
Authors:: Hayamizu, Kenji
Terayama, Naoki
Hashizume, Daisuke
Dodo, Kosuke
Sodeoka, Mikiko
Abstract:: Abstract: Chiral Pd‐BINAP complexes catalyze enantioselective Michael and fluorination reactions of β‐ketoamides and β‐ketoesters in which Pd‐enolate intermediates play a key role.
Is Part Of:: ChemInform. Volume 46:Issue 50(2015)
Journal:: ChemInform
Issue:: Volume 46:Issue 50(2015)
Issue Display:: Volume 46, Issue 50 (2015)
Year:: 2015
Volume:: 46
Issue:: 50
Issue Sort Value:: 2015-0046-0050-0000
Page Start:: no
Page End:: no
Publication Date:: 2015-12
Subjects:: diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) -- C‐C bond formation -- halogenation
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.201550025 ↗
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:: 266.xml