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Pregled bibliografske jedinice broj: 41752

Mercuration of thiophene-2-carboxylic acid, 2-thienylethanoic acid and 3-(2-thienil)alanine : preparation and spectral characterization


Popović, Zora; Soldin, Željka; Plavec, Janez; Vikić-Topić, Dražen
Mercuration of thiophene-2-carboxylic acid, 2-thienylethanoic acid and 3-(2-thienil)alanine : preparation and spectral characterization // Applied organometallic chemistry, 14 (2000), -; 598-603 (međunarodna recenzija, članak, znanstveni)


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Naslov
Mercuration of thiophene-2-carboxylic acid, 2-thienylethanoic acid and 3-(2-thienil)alanine : preparation and spectral characterization

Autori
Popović, Zora ; Soldin, Željka ; Plavec, Janez ; Vikić-Topić, Dražen

Izvornik
Applied organometallic chemistry (0268-2605) 14 (2000); 598-603

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
direct mercuration; 2-thienyl derivatives; IR; NMR

Sažetak
Thiophene-2-carboxylic acid, 2-thienyl etanoic acid and 3-(2-thienyl)-alanine were mercurated with mercury(II) chloride in aqueous media in the presence of sodium acetate trihydrate. Monomercurated and dimercurated products were obtained depending on the reaction conditions. When mercury(II) acetate was used as the mercuration agent the mixture of mono- and dimercurated products was obtained.The chemical formula and the structure of isolated compounds were deduced from elemental chemical analysis and IR spectra. In the case of soluble products the site and degree of mercuration were determined on the basis of 1^H and 13^C NMR spectra. In monomercurated thiophene-2-carboxylic acid, 2-thienyletanoic acid and 3-(2-thienyl)-alanine the H-5 signal is absent, which together with large downfield shift of the corresponding 13^C signal (ca. 24 and 21 ppm) confirmed that mercuration took place at the C-5. Two- and three-bond 199^Hg-13^C satellite couplings at the C-4 and C-3 as well as four-bond 199^Hg-1^H coupling at the H-4 were also revealed.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
00980802
119408

Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb

Profili:

Avatar Url Dražen Vikić-Topić (autor)

Avatar Url Željka Soldin (autor)

Avatar Url Zora Popović (autor)


Citiraj ovu publikaciju:

Popović, Zora; Soldin, Željka; Plavec, Janez; Vikić-Topić, Dražen
Mercuration of thiophene-2-carboxylic acid, 2-thienylethanoic acid and 3-(2-thienil)alanine : preparation and spectral characterization // Applied organometallic chemistry, 14 (2000), -; 598-603 (međunarodna recenzija, članak, znanstveni)
Popović, Z., Soldin, Ž., Plavec, J. & Vikić-Topić, D. (2000) Mercuration of thiophene-2-carboxylic acid, 2-thienylethanoic acid and 3-(2-thienil)alanine : preparation and spectral characterization. Applied organometallic chemistry, 14 (-), 598-603.
@article{article, author = {Popovi\'{c}, Zora and Soldin, \v{Z}eljka and Plavec, Janez and Viki\'{c}-Topi\'{c}, Dra\v{z}en}, year = {2000}, pages = {598-603}, keywords = {direct mercuration, 2-thienyl derivatives, IR, NMR}, journal = {Applied organometallic chemistry}, volume = {14}, number = {-}, issn = {0268-2605}, title = {Mercuration of thiophene-2-carboxylic acid, 2-thienylethanoic acid and 3-(2-thienil)alanine : preparation and spectral characterization}, keyword = {direct mercuration, 2-thienyl derivatives, IR, NMR} }
@article{article, author = {Popovi\'{c}, Zora and Soldin, \v{Z}eljka and Plavec, Janez and Viki\'{c}-Topi\'{c}, Dra\v{z}en}, year = {2000}, pages = {598-603}, keywords = {direct mercuration, 2-thienyl derivatives, IR, NMR}, journal = {Applied organometallic chemistry}, volume = {14}, number = {-}, issn = {0268-2605}, title = {Mercuration of thiophene-2-carboxylic acid, 2-thienylethanoic acid and 3-(2-thienil)alanine : preparation and spectral characterization}, keyword = {direct mercuration, 2-thienyl derivatives, IR, NMR} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


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