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Rubber Chemistry and Technology, 1966
Abstract Three technically feasible routes have now been established for preparation of linear perfluoroalkylene triazine polymers. The most advanced route is based on addition polymerization of long chain fluorocarbon dinitriles and diamidines, followed by acylation and cyclodehydration to triazine polymer.
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Abstract Three technically feasible routes have now been established for preparation of linear perfluoroalkylene triazine polymers. The most advanced route is based on addition polymerization of long chain fluorocarbon dinitriles and diamidines, followed by acylation and cyclodehydration to triazine polymer.
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2001
[290-38-0] C3H3N3 (MW 81.09) InChI = 1S/C3H3N3/c1-2-5-6-3-4-1/h1-3H InChIKey = FYADHXFMURLYQI-UHFFFAOYSA-N (electron-deficient heteroaromatic azadiene capable of participation in inverse electron demand Diels–Alder reactions with electron-rich dienophiles1) Alternate Names: as-triazine; α-triazine; isotriazine ...
Dale L. Boger, Minsheng Zhang
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[290-38-0] C3H3N3 (MW 81.09) InChI = 1S/C3H3N3/c1-2-5-6-3-4-1/h1-3H InChIKey = FYADHXFMURLYQI-UHFFFAOYSA-N (electron-deficient heteroaromatic azadiene capable of participation in inverse electron demand Diels–Alder reactions with electron-rich dienophiles1) Alternate Names: as-triazine; α-triazine; isotriazine ...
Dale L. Boger, Minsheng Zhang
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1976
Publisher Summary This chapter provides a comprehensive review of developments in 1,2,3-triazine chemistry from 1960 to the beginning of 1974. There are relatively few methods available for the preparation of condensed 1,2,3-triazines. The most commonly employed procedure is diazotization of a suitably ortho-substituted aniline or aminosubstituted ...
Ryszard J. Kobylecki, Alexander Mckillop
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Publisher Summary This chapter provides a comprehensive review of developments in 1,2,3-triazine chemistry from 1960 to the beginning of 1974. There are relatively few methods available for the preparation of condensed 1,2,3-triazines. The most commonly employed procedure is diazotization of a suitably ortho-substituted aniline or aminosubstituted ...
Ryszard J. Kobylecki, Alexander Mckillop
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Triazines. XXII. Fluoro-s-triazines
Journal of the American Chemical Society, 1959Ehrenfried Kober, Christoph Grundmann
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Triazine-based condensing reagents
Biopolymers, 2000The synthesis, properties, and application of condensing reagents derived from 1,3,5-triazines are described. The mechanism of activation of carboxylic function, structure of reactive intermediates, and mechanism of acylation of nucleophiles are presented.
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