ChemInform Abstract: A Straightforward and Highly Diastereoselective Access to Functionalized Monofluorinated Cyclopropanes via a Michael Initiated Ring Closure Reaction. Issue 11 (18th March 2014)

Record Type:: Journal Article
Title:: ChemInform Abstract: A Straightforward and Highly Diastereoselective Access to Functionalized Monofluorinated Cyclopropanes via a Michael Initiated Ring Closure Reaction. Issue 11 (18th March 2014)
Main Title:: ChemInform Abstract: A Straightforward and Highly Diastereoselective Access to Functionalized Monofluorinated Cyclopropanes via a Michael Initiated Ring Closure Reaction.
Authors:: Ferrary, Thibault
David, Emilie
Milanole, Gaelle
Besset, Tatiana
Jubault, Philippe
Pannecoucke, Xavier
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>A tandem Michael addition/ring closure sequence is developed to yield fluorinated cyclopropanes from a reaction of ammonium salts (I) derived from bromofluoroacetate and DABCO with electron deficient alkenes.</p> </abstract>
Is Part Of:: ChemInform. Volume 45:Issue 11(2014)
Journal:: ChemInform
Issue:: Volume 45:Issue 11(2014)
Issue Display:: Volume 45, Issue 11 (2014)
Year:: 2014
Volume:: 45
Issue:: 11
Issue Sort Value:: 2014-0045-0011-0000
Page Start:: no
Page End:: no
Publication Date:: 2014-03-18
Subjects:: 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.201411056 ↗
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:: 4241.xml