## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Synthesis and reactivity of some 3,4-dibromo-2H-[1]benzopyrans: The generation and reactions of 3,4-didehydro-2H-[1]benzopyran
β Scribed by Christopher D. Gabbutt; John D. Hepworth; B.Mark Heron; Md.Moshfiqur Rahman; Simon J. Coles; Michael B. Hursthouse
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 785 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
Reaction of 3,2,
6,
benzopyran with either organolithium reagents or magnesium generates the novel strained alkyne, 3,4-didehydro-2H-[1]benzopyran. Cycloaddition with furans gives access to the dibenzo[b,d]pyran system.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## 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