ChemInform Abstract: Lewis Base Catalyzed Trialkylsilylcyanide Additions to Cyclic 2‐Fluoroketones: Nucleophile Directed Access to Both cis‐ and trans‐Stereoisomers. Issue 36 (August 2016)

Record Type:: Journal Article
Title:: ChemInform Abstract: Lewis Base Catalyzed Trialkylsilylcyanide Additions to Cyclic 2‐Fluoroketones: Nucleophile Directed Access to Both cis‐ and trans‐Stereoisomers. Issue 36 (August 2016)
Main Title:: ChemInform Abstract: Lewis Base Catalyzed Trialkylsilylcyanide Additions to Cyclic 2‐Fluoroketones: Nucleophile Directed Access to Both cis‐ and trans‐Stereoisomers.
Authors:: Brawley, Kayla K.
Davis, Todd A.
Abstract:: Abstract: Cyclic 2‐fluoroketones react with cyanide (II) and iPr2 NEt as the catalyst to give cis‐addition product predominantly, whereas methoxide catalyzed reactions with cyanide (V) favour the formation of trans‐addition products.
Is Part Of:: ChemInform. Volume 47:Issue 36(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 36(2016)
Issue Display:: Volume 47, Issue 36 (2016)
Year:: 2016
Volume:: 47
Issue:: 36
Issue Sort Value:: 2016-0047-0036-0000
Page Start:: no
Page End:: no
Publication Date:: 2016-08
Subjects:: diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) -- addition reactions -- cyanation, nitrile formation
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.201636017 ↗
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:: 1740.xml