ChemInform Abstract: Reductive Cyclization of Halo‐Ketones to Form 3‐Hydroxy‐2‐oxindoles via Palladium Catalyzed Hydrogenation: A Hydrogen‐Mediated Grignard Addition. Issue 48 (December 2015)

Record Type:: Journal Article
Title:: ChemInform Abstract: Reductive Cyclization of Halo‐Ketones to Form 3‐Hydroxy‐2‐oxindoles via Palladium Catalyzed Hydrogenation: A Hydrogen‐Mediated Grignard Addition. Issue 48 (December 2015)
Main Title:: ChemInform Abstract: Reductive Cyclization of Halo‐Ketones to Form 3‐Hydroxy‐2‐oxindoles via Palladium Catalyzed Hydrogenation: A Hydrogen‐Mediated Grignard Addition.
Authors:: Shin, Inji
Ramgren, Stephen D.
Krische, Michael J.
Abstract:: Abstract: The reductive cyclization of halodiketones (I) and (III) provides the corresponding oxindole derivatives in moderate to excellent yields.
Is Part Of:: ChemInform. Volume 46:Issue 48(2015)
Journal:: ChemInform
Issue:: Volume 46:Issue 48(2015)
Issue Display:: Volume 46, Issue 48 (2015)
Year:: 2015
Volume:: 46
Issue:: 48
Issue Sort Value:: 2015-0046-0048-0000
Page Start:: no
Page End:: no
Publication Date:: 2015-12
Subjects:: indole derivatives, isoindole derivatives -- ring closure reactions, annulation reactions -- benzofuran derivatives
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.201548128 ↗
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:: 2615.xml