ChemInform Abstract: A Sequential Pd/Norbornene‐Catalyzed Process Generates o‐Biaryl Carbaldehydes or Ketones via a Redox Reaction or 6H‐Dibenzopyrans by C—O Ring Closure. Issue 14 (20th March 2013)

Record Type:: Journal Article
Title:: ChemInform Abstract: A Sequential Pd/Norbornene‐Catalyzed Process Generates o‐Biaryl Carbaldehydes or Ketones via a Redox Reaction or 6H‐Dibenzopyrans by C—O Ring Closure. Issue 14 (20th March 2013)
Main Title:: ChemInform Abstract: A Sequential Pd/Norbornene‐Catalyzed Process Generates o‐Biaryl Carbaldehydes or Ketones via a Redox Reaction or 6H‐Dibenzopyrans by C—O Ring Closure.
Authors:: Motti, Elena
Della Ca, Nicola
Xu, Di
Piersimoni, Anna
Bedogni, Elena
Zhou, Zhi‐Ming
Catellani, Marta
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>An excess of norbornene has to be used, the molar ratio of norbornene to Pd varies between 5:1 to 20:1.</p> </abstract>
Is Part Of:: ChemInform. Volume 44:Issue 14(2013)
Journal:: ChemInform
Issue:: Volume 44:Issue 14(2013)
Issue Display:: Volume 44, Issue 14 (2013)
Year:: 2013
Volume:: 44
Issue:: 14
Issue Sort Value:: 2013-0044-0014-0000
Page Start:: no
Page End:: no
Publication Date:: 2013-03-20
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.201314095 ↗
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:: 3964.xml