ChemInform Abstract: Synthesis of 9H‐Pyrrolo[1, 2‐a]indole and 3H‐Pyrrolizine Derivatives via a Phosphine‐Catalyzed Umpolung Addition/Intramolecular Wittig Reaction. Issue 40 (September 2016)

Record Type:: Journal Article
Title:: ChemInform Abstract: Synthesis of 9H‐Pyrrolo[1, 2‐a]indole and 3H‐Pyrrolizine Derivatives via a Phosphine‐Catalyzed Umpolung Addition/Intramolecular Wittig Reaction. Issue 40 (September 2016)
Main Title:: ChemInform Abstract: Synthesis of 9H‐Pyrrolo[1, 2‐a]indole and 3H‐Pyrrolizine Derivatives via a Phosphine‐Catalyzed Umpolung Addition/Intramolecular Wittig Reaction.
Authors:: Saleh, Nidal
Voituriez, Arnaud
Abstract:: Abstract: Optimized reaction conditions are developed for the title process allowing cyclization reactions of heteroaryl aldehydes (I) or (IV) with acetylene dicarboxylate (II) to form the title products in high yields.
Is Part Of:: ChemInform. Volume 47:Issue 40(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 40(2016)
Issue Display:: Volume 47, Issue 40 (2016)
Year:: 2016
Volume:: 47
Issue:: 40
Issue Sort Value:: 2016-0047-0040-0000
Page Start:: no
Page End:: no
Publication Date:: 2016-09
Subjects:: fused pyrrole derivatives -- ring closure reactions, annulation reactions
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.201640131 ↗
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:: 2380.xml