3-Ethynylthiophene may be used in the synthesis of the following:
1-(2-bromobenzyl)-4-(thiophen-3-yl)-1H-1,2,3-triazole which is obtained by heating with 2-iodophenylethylazide in the presence of copper acetate monohydrate catalyst in N-methyl-2-pyrrolidone[1]
N-benzyl-1-phenyl-5-(thiophen-3-yl)-4-pentyn-2-amine via a multi-step reaction process[2]
[(C4H3S-3)C≡CAg]n, a polymeric compound obtained via reaction with silver nitrate in the presence of triethylamine in acetonitrile[3]
4,5-bis(thiophen-3-ylethynyl)phthalonitrile via Sonogashira cross-coupling reaction with 4,5-dichlorophthalonitrile[4]
"An easy synthetic approach to 1, 2, 3-triazole-fused heterocycles"
Fiandanese V, et al.
Tetrahedron, 66(46), 8846-8853 (2010)
"Silver (I)- Thiophene p Interaction in the Assembly of Coordination Networks with the Supramolecular Synthons R- C? C? Ag n (R= 2-or 3-thienyl; n= 4)"
Zhao L, et al.
Organometallics, 26(18), 4439- 4448 (2007)
"Synthesis and photophysical properties of novel unsymmetrical metal-free and metallophthalocyanines"
Ozcesmeci I, et al.
Journal of Organometallic Chemistry, 750, 125-131 (2014)
"Synthesis, analysis of spectroscopic and nonlinear optical properties of the novel compound:(S)-N-benzyl-1-phenyl-5-(thiophen-3-yl)-4-pentyn-2-amine"
Karabacak M, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 97, 556-567 (2012)
Chitosan is an abundant and renewable polysaccharide, which exhibits attractive bioactivities and natural properties. Improvement such as chemical modification of chitosan is often performed for its potential of providing high bioactivity and good water solubility. A new class of chitosan
The terminal alkyne functionality has a wide range of applications including most recently the synthesis of spiropyran substituted 2,3-dicyanopyrazines and (±)-asteriscanolide, as well as conversion to enamines using resin-bound 2° amines.