Photochemistry of 2-cyanofuran
โ Scribed by C.J. Samuel; N. Rowlands
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 291 KB
- Volume
- 78
- Category
- Article
- ISSN
- 1010-6030
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
We found that on boiling in high-boiling solvents, 2-amino-5-aryl-4,5-dihydro-2-aminofurans rearrange with the formation of amides of cyanocyclopropanecarboxylic acids.
The photochemistry of medium ring-cycloalkanones typified by cyclododecan-
Direct irradiation of B,y-unsaturated ketones with accessible allylic yhydrogens has been reported to yield intramolecular y-hydrogen abstraction,' intramolecular cycloaddition'e and 1,3-acyl shift and a-cleavage processes la,b,f . As part of a study of the effect of stereochemistry on the relative
Regioselective Synthesis of 2-Amino-3-cyanofuran Derivatives and Its Guanidine Cyclization Reaction. -The title cyclization reaction leads to the unexpected pyrrolo pyrimidines (V) and (VIII) rather than the expected furopyrimidines.