Pregled bibliografske jedinice broj: 254722
Chiroptical properties and enantioselectivity in hydrogenation with rhodium(I) complexes of chiral bis-diphenylphosphines derived from D-glucose and D-galactose
Chiroptical properties and enantioselectivity in hydrogenation with rhodium(I) complexes of chiral bis-diphenylphosphines derived from D-glucose and D-galactose // Journal of Organometallic Chemistry, 370 (1989), 1-3; 295-304 doi:10.1016/0022-328X(89)87293-6 (međunarodna recenzija, članak, znanstveni)
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Naslov
Chiroptical properties and enantioselectivity in hydrogenation with rhodium(I) complexes of chiral bis-diphenylphosphines derived from D-glucose and D-galactose
Autori
Šunjić, Vitomir ; Habuš, Ivan ; Snatzke, Gunter
Izvornik
Journal of Organometallic Chemistry (0022-328X) 370
(1989), 1-3;
295-304
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Z-α -acetylaminocinnamic acid ; α -acetylaminoacrylic acid ; bidentate ligands (3 ; 6)
Sažetak
(2R, 3S)-2-Diphenylphosphinomethyl-3-diphenylphosphinotetrahydropyran (3) has been prepared in 64% yield from the dimesylate 5, derived from D-galactose. The surprisingly different reactivities of dimesylates 2 and 5 towards diphenylphosphide anion are considered and the conformational properties of 1-6 discussed in terms of their CD spectra. The rhodium(I) complexes 9 and 10 exhibit low to relatively high enantioselectivities in hydrogenation of Z-α -acetylaminocinnamic acid and α -acetylaminoacrylic acid. The chiroptical and conformational properties of the bidentate ligands (3, 6), and their rhodium(I) complexes (9, 10) are correlated with the observed enantioselectivities.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb
Citiraj ovu publikaciju:
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