Stereo- and regioselectivity of intramolecular 1,2-arene-alkene photocycloaddition in 2-alkenyl-4-chromanones
โ Scribed by Govind P. Kalena; Padmanava Pradhan; Asoke Banerji
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 720 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
โฆ Synopsis
Intramolecular 1,2-arone-alkene photocycloaddition of 2-alkenyl-4-chromanoues gave complex multicyclic oxatctracyclotetradecanediones which on internal photo-and microwave induced thermal rearrangements provided a diverse array of compounds with [3.3.0]bieyclooetane carbon frame work. The stereoand regioehemical aspects as well as desymmetrization of alkenyl chromanones due to intramolecolar 1,2-aronealkene photocycloaddition have also been discussed.
๐ SIMILAR VOLUMES
On irradiation, 2-methyl-2-ethenyl naphtha-4-chromanone 1 undergoes an unusual intramolecular arene-alkene photocyclisation, followed by rearrangements to give a [5.3.1.0 6,1 ]benzotricycloundecene, 5.
## 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 of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v