๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Determination of enantiomeric purity of axially chiral biaryls

โœ Scribed by Kuninobu Kabuto; Fujiko Yasuhara; Shozo Yamaguchi


Publisher
Elsevier Science
Year
1980
Tongue
French
Weight
125 KB
Volume
21
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis


Sumnary: Enantlomenc purities of axially choral biaryls with hydroxyl, amino, and carboxyl groups can be easily determlned by pmr spectra using MTPA derivatives and shift reagent. Recently, Behnam et al. have reported' that the methyl proton signals in racemlc biaryls such as dimethyl 6,6'-dlmethoxy-2,2'-dlphenate were separated Into two peaks in the presence of


๐Ÿ“œ SIMILAR VOLUMES


Determination of absolute configuration
โœ Kuninobu Kabuto; Fujiko Yasuhara; Shozo Yamaguchi ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 273 KB

Sutmnary: Absolute configurations of axially chiral biaryls with hydroxyl, amino, and carboxyl groups can be easily determined by pmr spectra using MTPA derivatives and shift reagents. Recently chiral biaryls have been successfully utilized in the field of asynetric synthesis\*. For example, virtual

Determination of enantiomeric purity of
โœ J. Bus; C.M. Lok; A. Groenewegen ๐Ÿ“‚ Article ๐Ÿ“… 1976 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 518 KB

Tris(3-heptafluorobutyryl-d-camphorato)europium(Ill), Eu(hfbc) 3 was used to determine the optical purities of enantiomeric mixtures of tri-, di-and monoglycerides with various fatty acid chain lengths by proton magnetic resonance (PMR). Synthesized model enantiomers were used to assign PMR signals.

Determination of enantiomeric purity of
โœ Ernest L. Eliel; Kwang-Youn Ko ๐Ÿ“‚ Article ๐Ÿ“… 1983 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 242 KB

The enantiomeric purity of primary-secondary glycols, RCHOHCH2OH, is conveniently determined by conversion to a pair of epimeric 1,3-dioxolanes through condensation with bensaldehyde, followed by nmr spectroscopy in presence of a chiral shift reagent with observation of the bensylic protons.

O-nitromandelic acid: A chiral solvating
โœ Mohammed A. Haiza; Amitav Sanyal; John K. Snyder ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 98 KB ๐Ÿ‘ 2 views

O-Nitromandelic acid, easily prepared from either enantiomer of mandelic acid, has been used as a chiral solvating agent for the determination of enantiomeric purity of several diamine derivatives and other compounds using 1 H NMR spectroscopy.