a b Alexandru T. Baaban,-Teodor S i l v i u Balaban,' Cornelia Uncuta,a b Mircea D. Gheorghiu,-and F i l i p Chiraleu - a Polytechnic I n s t i t u t e , Organic Chemistry Department, S p l a i u l Independentei 31 3, 76206 Bucharest, Roumania a Center for Organic Chemistry -ICECHIM. Bucharest, Rou
Formation of 6,6-dimethyl-2,4-cyclohexadienylidene-1-imines from primary amines and 2,6-diisopropylpyrylium salts
โ Scribed by Cornelia Uncuta; Mircea D Gheorgiu; Alexandru T Balaban
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 145 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
2,6-Diisopropyz .-substituted pyryliwn salts 5 react with primary wnines RNH, yielding pyridinium salts, g, and 6,6-dimethyl-2,4-eyclohesadi&yZidene-l-iminium salts, z, in relative cmwunts depending on the group R (160/O for R = Me, 4317 for R = Et, 20/80 for R = iPr, and O/G for R = tBul urovinq that steric factors are as important as aromatic delocaZization in AkROkC reactions Lf pyrylium salts.
๐ SIMILAR VOLUMES
In this article, the chemical modification of poly(2,6-dimethyl-l,4-phenylene oxide) (PPO) was carried out by incorporating a n amine group into the PPO backbone. A maximum monosubstitution degree of 65 mol % was reached. The effects of reaction conditions on the functional group content in PPO is d