126965-23-9Relevant academic research and scientific papers
2,2-DIMETHYL-5-(5-R-FURFURYLIDENE)-1,3-DIOXANE-4,6-DIONES. 3. SELECTIVE HYDROGENATION OF THE EXOCYCLIC DOUBLE BOND AND THREE-DIMENSIONAL STRUCTURES OF THE REACTION PRODUCTS
Krapivin, G. D.,Zavodnik, V. E.,Val'ter, N. I.,Bel'skii, V. K.,Kul'nevich, V. G.
, p. 1005 - 1011 (1989)
The reaction of 2,2-dimethyl-5-(5-R-furfurylidene)-1,3-dioxane-4,6-diones with sodium borohydride in alcohol leads exclusively to products of hydrogenation of the exocyclic double bond.The three-dimensional structure of one of them - 2,2-dimethyl-5-(5-met
SYNTHESIS AND PROPERTIES OF 5-PHENYLETHYNYLFURAN-2-ALDEHYDE
Zavodnov, V. S.,Kul'nevich, V. G.,Zinov'ev, V. D.
, p. 386 - 389 (2007/10/02)
Phenylethynylation of 5-halofurfurals gives 5-phenylethynylfuran-2-aldehyde which can be converted into the corresponding acid and several of its derivatives with retention of the triple bond.
