Structure of optically active polymers from esters of methacrylic and itaconic acids
β Scribed by Ye.I. Klabunovskii; B.V. Lopatin; L.G. Vorontsova; Yu.I. Petrov; M.I. Shvartsman
- Book ID
- 118356893
- Publisher
- Elsevier Science
- Year
- 1964
- Weight
- 269 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0032-3950
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## Abstract For Abstract see ChemInform Abstract in Full Text.
Acyloxy)alkyl esters are commonly employed as prodrugs of carboxylic acid containing compounds. Several optically active (acyloxy)alkyl esters are prepared from a coupling and rearrangement reaction between optically active O-acyl-a-hydroxy acids and 3-chloroperoxybenzoic acid mediated by diisopropy
## Abstract The synthesis of a novel optically active methacrylic monomer containing in the side chain the (__S__)β3βhydroxyβ__N__βphenyl pyrrolidine ring linked to a 4βcyanophenylazocarbazole moiety [(__S__)β**MCAPP**β**C**] and of the analogous achiral monomer (**MCAPEβC**) is described. Both the
## Abstract The photochromic and photoresponsive properties of a series of optically active azoaromatic polymers, containing in the side chain the rigid (__S__)β and/or (__R__)βhydroxysuccinimide residue, have been investigated in solution and in the solid state as thin films by observing the __tra