ChemInform Abstract: Dehydrogenative N‐Heterocyclization of 2‐(2‐Aminoaryl)ethyl Alcohols to Indole Derivatives Catalyzed by (μ‐Oxo)tetraruthenium Cluster/1, 2‐Bis(diphenylphosphino)benzene. Issue 17 (4th April 2013)

Record Type:: Journal Article
Title:: ChemInform Abstract: Dehydrogenative N‐Heterocyclization of 2‐(2‐Aminoaryl)ethyl Alcohols to Indole Derivatives Catalyzed by (μ‐Oxo)tetraruthenium Cluster/1, 2‐Bis(diphenylphosphino)benzene. Issue 17 (4th April 2013)
Main Title:: ChemInform Abstract: Dehydrogenative N‐Heterocyclization of 2‐(2‐Aminoaryl)ethyl Alcohols to Indole Derivatives Catalyzed by (μ‐Oxo)tetraruthenium Cluster/1, 2‐Bis(diphenylphosphino)benzene.
Authors:: Kondo, Teruyuki
Kanda, Takashi
Takagi, Daisuke
Wada, Kenji
Kimura, Yu
Toshimitsu, Akio
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The novel title catalyst system enables a simple, selective, and practical synthesis of indoles from aminoalcohols.</p> </abstract>
Is Part Of:: ChemInform. Volume 44:Issue 17(2013)
Journal:: ChemInform
Issue:: Volume 44:Issue 17(2013)
Issue Display:: Volume 44, Issue 17 (2013)
Year:: 2013
Volume:: 44
Issue:: 17
Issue Sort Value:: 2013-0044-0017-0000
Page Start:: no
Page End:: no
Publication Date:: 2013-04-04
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.201317103 ↗
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:: 3719.xml