The oxyiodination of 5,8-dimethoxy-1,4-dihydro-1,4-ethanonaphthalene
โ Scribed by Smith, William B.
- Book ID
- 126922131
- Publisher
- American Chemical Society
- Year
- 1985
- Tongue
- English
- Weight
- 567 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0022-3263
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๐ SIMILAR VOLUMES
We have previously reported photoisomerisation reactions of tetrafluorobenzobarrelene both in the presence, and in the absence of triplet sensitisers. 1 The photoisomerisations of barrelene,2 substituted barrelenes, 3 and benzobarrelene 4 and derivatives5 have also been studied.
Synthesis of 4,8โDimethoxyโ1,5โnaphthalenediol and Its Oxidation to 4,8โDimethoxyโ1,5โnaphthoquinone Formation of the new 1,5โnaphthoquinone 3 was achieved by methylation of 1,4,5,8โnaphthalenetetrol (1a) and oxidation of the dimethyl ether 1c obtained thereof. In the presence of water, 3 yields th