Synthesis of 3-benzoyl-3,4-dihydro-2H- and 3,4-dihydro-2,2-disubstituted-benzopyrans via alkynyl grignard reagents
β Scribed by Emmanuel A. Adegoke; T. A. Emokpae; H. Ephraim-Bassey; C. A. Oyelola
- Book ID
- 112128771
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1987
- Tongue
- English
- Weight
- 288 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0022-152X
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Highly enantioselective reduction of 3,4-dihydro-2,2-dimethyl-2H-l-benzopyran-4-ones 3 s-e by BH3 was achieved in the presence of catalytic amounts of Corey's oxazaborolidine 4 to afford the corresponding 3,4-dihydro-2,2dimetbyl-2H-l-~nzopyran-4-ols 2a-e in quantitative yields. These benzopyran-4-ol
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A simple method for the preparation of 4,4-disubstituted-3,4-dihydro-1H-2,1,3-benzothiadiazine 2,2dioxides is described. Treatment of N-sulfonyl ketimines 2 and 3 with different carbon nucleophiles afforded the corresponding of 4,4-disubstituted-3,4-dihydro-1H-2,1,3-benzothiadiazine 2,2-dioxides 1 i