ChemInform Abstract: An Efficient Transformation of Furano‐Hydroxychalcones to Furanoflavones via Base Mediated Intramolecular Tandem O‐Arylation and C—O Bond Cleavage: A New Approach for the Synthesis of Furanoflavones. Issue 9 (February 2016)

Record Type:: Journal Article
Title:: ChemInform Abstract: An Efficient Transformation of Furano‐Hydroxychalcones to Furanoflavones via Base Mediated Intramolecular Tandem O‐Arylation and C—O Bond Cleavage: A New Approach for the Synthesis of Furanoflavones. Issue 9 (February 2016)
Main Title:: ChemInform Abstract: An Efficient Transformation of Furano‐Hydroxychalcones to Furanoflavones via Base Mediated Intramolecular Tandem O‐Arylation and C—O Bond Cleavage: A New Approach for the Synthesis of Furanoflavones.
Authors:: Sharma, Rajni
Vishwakarma, Ram A.
Bharate, Sandip B.
Abstract:: Abstract: A new approach for the synthesis of the natural furanoflavones lanceolatin B (IIa) and pongaglabrone (IIb) from corresponding furano‐hydroxychalcones (I) under mild, metal‐free conditions is given.
Is Part Of:: ChemInform. Volume 47:Issue 9(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 9(2016)
Issue Display:: Volume 47, Issue 9 (2016)
Year:: 2016
Volume:: 47
Issue:: 9
Issue Sort Value:: 2016-0047-0009-0000
Page Start:: no
Page End:: no
Publication Date:: 2016-02
Subjects:: other bioactive products -- ring closure reactions, annulation reactions -- benzopyran derivatives
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.201609216 ↗
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:: 535.xml