## Abstract magnified image The Chemistry and application of the title aldehyde and some simple derivatives thereof are reviewed.
Studies in chromone derivatives: cycloaddition reactions of 4-oxo 4h-1-benzopyran-3-carboxaldehyde imines with benzonitrile oxide and nitrilimine of 4-oxo-4h-1-benzopyran-3-carboxaldehyde with alkenes
β Scribed by Arpan Kumar Baruah; Dipak Prajapati; Jagir Singh Sandhu
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 474 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
The chromone fmfn s 1 and benzonitrile oxide reacted regioapaciffcally to yield 6 1 -172,4 oxadiarolinyl chromonea 2_in good yields. Also the preparation of a novel dipole & derived from f-formylchromons and its cycloaddition reactions with a variety of alkenes which gave pyrazolinyl chromones zia described. I242 A. K. B.UWAH et al. sit. salactivity follouad by th. dipole 14 and oyclaaddition ocaurring only l aroaa the azomethina Punction leaving chromona double bond intact.
π SIMILAR VOLUMES
Studies on Chromone Derivatives: Microwave Assisted 1,3-Dipolar Cycloaddition Reactions of 4-Oxo-1-benzopyran-3-carboxaldehyde Imine Oxides. -The title reaction using microwaves (2450 MHz) gives higher yields and needs shorter reaction times compared to the thermal cycloaddition (45-60%, 12-48 h).
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## Abstract magnified image The title aldehyde **1** reacts smoothly with the enamine moiety of **2**βaminochromone **2** to produce hitherto unreported 3β(2βhydroxybenzoyl)β5__H__β1βbenzopyrano[2,3β__b__]pyridinβ5βone (azaxanthone) **5**. This reaction has been extended for the synthesis of bisaz