ChemInform Abstract: Highly Enantioselective Monofluoromethylation of C2‐Arylindoles Using FBSM under Chiral Phase‐Transfer Catalysis. Issue 48 (26th November 2013)

Record Type:: Journal Article
Title:: ChemInform Abstract: Highly Enantioselective Monofluoromethylation of C2‐Arylindoles Using FBSM under Chiral Phase‐Transfer Catalysis. Issue 48 (26th November 2013)
Main Title:: ChemInform Abstract: Highly Enantioselective Monofluoromethylation of C2‐Arylindoles Using FBSM under Chiral Phase‐Transfer Catalysis.
Authors:: Matsuzaki, Kohei
Furukawa, Tatsuya
Tokunaga, Etsuko
Matsumoto, Takashi
Shiro, Motoo
Shibata, Norio
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The enantioselective addition of 1‐fluoro‐1, 1‐bis(phenylsulfonyl)methane (II) to vinylogous imines generated in situ from 2‐aryl‐3‐(1‐arylsulfonylmethyl)indoles is achieved using chiral ammonium salts derived from cinchona alkaloids as phase‐transfer catalysts.</p> </abstract>
Is Part Of:: ChemInform. Volume 44:Issue 48(2013)
Journal:: ChemInform
Issue:: Volume 44:Issue 48(2013)
Issue Display:: Volume 44, Issue 48 (2013)
Year:: 2013
Volume:: 44
Issue:: 48
Issue Sort Value:: 2013-0044-0048-0000
Page Start:: no
Page End:: no
Publication Date:: 2013-11-26
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.201348135 ↗
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:: 3377.xml