The reaction of furan derivatives with azo-bis-isobutyronitrile
β Scribed by A. Gandini; J. Rieumont
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- French
- Weight
- 210 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The interaction of free radicals with furan has been studied previously, but only with alkaxy (11, bcnzoyl (2) and aromatic radicals (3-5). The addition reactions to give 2,5_dihydrofurans predominate, but in the case of the phenyl radicals (3-5) substitution at C-2 has been reported.
The mechanism of autoinhibition displayed by vinyl monomers containing the furan ring, such as vinyl 2-furoate (6-8), vinyl 2-fury1 acetate (8), vinyl 2-furylpropionate
π SIMILAR VOLUMES
A mixture of formaldehyde and aminoazobenzene condensed readily under physiological conditions to form covalently bound products with purines or pyrimidines and their corresponding nucleosides and nucleotides bearing amino groups. In the case of cytosine derivatives it was established that Mannich t
Attempts have been made on trifluoroacelJc acid catalysed Diels-Alder reaction of furan, 2,5-dimethylfuran and 2,5-diphenylfuran with ,8-ferroccnyl-a-enones. No Diels-Alder products were isolated or detected but products from the FriedeI-Crafls fl-alkylation of furan ring were prepared in some cases