Recyclization of methyl-4-hydroxy-2-(o-hydroxyphenylamino)-5-oxo-2,5-dihydropyrrole-2-carboxylate into the amide of (2-oxo-3,4-dihydro-2H-1,4-benzoxazin-3-ylidene)pyruvic acid
β Scribed by A. N. Maslivets; L. I. Smirnova; Yu. S. Andreichikov
- Publisher
- Springer US
- Year
- 1991
- Tongue
- English
- Weight
- 70 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0009-3122
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β¦ Synopsis
XIII are separated into the individual isomers by PTLC [preparative thin-layer chromatography] on silica gel plates. The structures of the compounds prepared were shown by means of PMR and confirmed by mass spectra obtained in a Finnigan MAT90 instrument with ionizing electrons of 70-eV energy and a source temperature of 200~ Despite the presence of labile substituents and the high temperature of vaporization of the samples, the latter were characterized by the maximum intensity of the molecular ion peaks.
Thus, we propose a simple and accessible method of introducing one or two functional groups into tetraarylporphyrin molecules that allows them to be used for further chemical transformations.
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π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
A general synthesis of new alkyl 4-alkyl-2-hydroxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate peptidomimetic building blocks from the corresponding alkyl 3-oxo-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylates through carbanion oxidation is described.