Results 241 to 250 of about 16,084 (302)
Some of the next articles are maybe not open access.
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
openaire +1 more source
[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
openaire +1 more source
ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
C. W. Lindsley, M. E. Layton
openaire +1 more source
AbstractFor Abstract see ChemInform Abstract in Full Text.
C. W. Lindsley, M. E. Layton
openaire +1 more source
Acta Crystallographica Section C Crystal Structure Communications, 1994
In 4,6-diamino-1-ethyl-2-(2-hydroxyphenyl)-1,2-dihydro-3H + ,5H + -1,3,5-triazinium sulfate monohydrate, C 11 H 17 N 5 O 2+ .SO 4 2- .H 2 O, the sulfate group and the triazine ring are bridged via N-H...O hydrogen bonds. The O atom of the water molecule forms O-H...O hydrogen bonds with the sulfate moieties of two neighbouring units and O...H-N ...
G. D. Nigam +3 more
openaire +1 more source
In 4,6-diamino-1-ethyl-2-(2-hydroxyphenyl)-1,2-dihydro-3H + ,5H + -1,3,5-triazinium sulfate monohydrate, C 11 H 17 N 5 O 2+ .SO 4 2- .H 2 O, the sulfate group and the triazine ring are bridged via N-H...O hydrogen bonds. The O atom of the water molecule forms O-H...O hydrogen bonds with the sulfate moieties of two neighbouring units and O...H-N ...
G. D. Nigam +3 more
openaire +1 more source
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.
openaire +1 more source
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.
openaire +1 more source
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
openaire +1 more source
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
openaire +1 more source
Triazines: Syntheses and Inverse Electron-demand Diels–Alder Reactions
Chemical Reviews, 2021Fa-Guang Zhang +2 more
exaly
Triazines. XXII. Fluoro-s-triazines
Journal of the American Chemical Society, 1959Ehrenfried Kober, Christoph Grundmann
openaire +1 more source