Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

3.4- Furan dicarboxylic acid ester derivative

The ultraviolet absorption spectra of compounds II from D-glucose and XI from D-fructose show an absorption band at 250 m/j, in accordance with their furan character.9 The product of periodate oxidation (V) and the dimethyl ester of the derived dicarboxylic acid (III) absorb at 285 and 262 m/i, respectively. The anhydrides of the condensates, XXXIV, do not exhibit selective absorption in the ultraviolet region, but the product of their oxidation (XXXVI) with periodic acid shows8 a band at about 270 m/i. [Pg.110]

A simple procedure to prepare 5-aryl- and 5-pyridyl-2-furaldehydes from inexpensive, commercially available 2-furaldehyde diethyl acetal was reported. The reaction proceeded in a four-step, one-pot procedure and the yield of coupling step was usually between 58-91% <02OL375>. A facile route to 3,4-furandicarboxylic acids was developed. DDQ-oxidation of 2,5-dihydrofuran derivatives, which were produced from dimethyl maleic anhydride, furnished the desired esters of furan-3,4-dicarboxylic acid <02S1010>. The furan-fused tetracyclic core of halenaquinol and halenaquinone possessing antibiotic, cardiotonic, and protein tyrosine kinase inhibitory activities was synthesized. Intramolecular cycloaddition of an o-quinodimethane with furan gave the adduct as a single isomer via an enrfo-transition state, which was converted to trisubstituted furan by oxidation-elimination reactions <02T6097>. [Pg.180]

In 1975, Kellyprepared and characterized a number of polyesters based on 2,5-disubstituted furans in various states of reduction. In this study, 2,5-disubstituted-furan, -dihydrofuran, and -tetrahydrofuran monomers were polymerized using solution, melt-transesterification, ring-opening, and interfacial techniques. These monomers included diacids, diols, diacid chlorides, diesters, dicarboxylic acid anhydrides, as well as monomers based on 5-hydroxymethyl-2-furoic and tetrahydrofuroic acids and esters, and bycyclic lactones containing the tetrahydrofuran ring. A thorough review of previous work done in the area of poljnner synthesis, based on 2,5-disubstituted furan derivatives is reported. It is reported that when... [Pg.54]


See other pages where 3.4- Furan dicarboxylic acid ester derivative is mentioned: [Pg.691]    [Pg.691]    [Pg.53]    [Pg.322]    [Pg.369]    [Pg.633]    [Pg.686]    [Pg.633]    [Pg.633]    [Pg.743]    [Pg.302]    [Pg.341]    [Pg.608]    [Pg.608]   
See also in sourсe #XX -- [ Pg.51 ]




SEARCH



2.5- dicarboxylic acid, derivatives

Dicarboxylate esters

Dicarboxylic acid ester

Dicarboxylic derivs

Dicarboxylic esters

Ester derivation

Ester derivatives

Furan derivatives

Furane derivatives

Furans esters

© 2024 chempedia.info