ChemInform Abstract: Highly Selective and Modular Synthesis of 3‐Aryl‐4‐(arylethynyl)‐2H‐chromen‐2‐ones from 2‐Iodoaryl 2‐Arylacetates Through a Carbonylative Sonogashira Coupling‐Intramolecular Aldol Cascade Reaction. Issue 52 (6th December 2016)

Record Type:
Journal Article
Title:
ChemInform Abstract: Highly Selective and Modular Synthesis of 3‐Aryl‐4‐(arylethynyl)‐2H‐chromen‐2‐ones from 2‐Iodoaryl 2‐Arylacetates Through a Carbonylative Sonogashira Coupling‐Intramolecular Aldol Cascade Reaction. Issue 52 (6th December 2016)
Main Title:
ChemInform Abstract: Highly Selective and Modular Synthesis of 3‐Aryl‐4‐(arylethynyl)‐2H‐chromen‐2‐ones from 2‐Iodoaryl 2‐Arylacetates Through a Carbonylative Sonogashira Coupling‐Intramolecular Aldol Cascade Reaction.
Authors:
Chandrasekhar, Attoor
Ramkumar, Venkatachalam
Sankararaman, Sethuraman
Abstract:
Abstract: A modular method for the synthesis of the title chromenones is developed based on a carbonylative Sonogashira coupling‐intramolecular aldol cascade reaction starting from iodoaryl arylacetates.
Is Part Of:
ChemInform. Volume 47:Issue 52(2016)
Journal:
ChemInform
Issue:
Volume 47:Issue 52(2016)
Issue Display:
Volume 47, Issue 52 (2016)
Year:
2016
Volume:
47
Issue:
52
Issue Sort Value:
2016-0047-0052-0000
Page Start:
no
Page End:
no
Publication Date:
2016-12-06
Subjects:
benzopyran derivatives -- catalysis, phase‐transfer catalysis -- ring closure reactions, annulation reactions -- carbonylation
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.201652286 ↗
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:
507.xml