ChemInform Abstract: Selective Synthesis of 6′‐Arylidene‐1‐aryl‐3‐aryl‐spiro[pyrrolizidine‐2, 2′‐cyclohexanone] by Cycloaddition of Azomethine Ylides to Dibenzylidene Cyclohexanone. Issue 36 (September 2015)

Record Type:: Journal Article
Title:: ChemInform Abstract: Selective Synthesis of 6′‐Arylidene‐1‐aryl‐3‐aryl‐spiro[pyrrolizidine‐2, 2′‐cyclohexanone] by Cycloaddition of Azomethine Ylides to Dibenzylidene Cyclohexanone. Issue 36 (September 2015)
Main Title:: ChemInform Abstract: Selective Synthesis of 6′‐Arylidene‐1‐aryl‐3‐aryl‐spiro[pyrrolizidine‐2, 2′‐cyclohexanone] by Cycloaddition of Azomethine Ylides to Dibenzylidene Cyclohexanone.
Authors:: Gayen, Biswajit
Banerji, Avijit
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Azomethine ylides, generated in situ from L‐proline and aryl aldehydes, undergo cycloaddition reaction to form spiro compounds of type (IV).</p> </abstract>
Is Part Of:: ChemInform. Volume 46:Issue 36(2015)
Journal:: ChemInform
Issue:: Volume 46:Issue 36(2015)
Issue Display:: Volume 46, Issue 36 (2015)
Year:: 2015
Volume:: 46
Issue:: 36
Issue Sort Value:: 2015-0046-0036-0000
Page Start:: no
Page End:: no
Publication Date:: 2015-09
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.201536132 ↗
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:: 4280.xml