Cover Picture: Inherently Chiral Molecular Clips: Synthesis, Chiroptical Properties, and Application to Chiral Discrimination (Chem. Eur. J. 9/2007) | Zendy

Fukuhara Gaku | Zendy; Madenci Süreyya | Zendy; Polkowska Jolanta | Zendy; Bastkowski Frank | Zendy; Klärner FrankGerrit | Zendy; Origane Yumi | Zendy; Kaneda Masayuki | Zendy; Mori Tadashi | Zendy; Wada Takehiko | Zendy; Inoue Yoshihisa | Zendy

Premium

Cover Picture: Inherently Chiral Molecular Clips: Synthesis, Chiroptical Properties, and Application to Chiral Discrimination (Chem. Eur. J. 9/2007)

Author(s) -

Fukuhara Gaku,

Madenci Süreyya,

Polkowska Jolanta,

Bastkowski Frank,

Klärner FrankGerrit,

Origane Yumi,

Kaneda Masayuki,

Mori Tadashi,

Wada Takehiko,

Inoue Yoshihisa

Publication year - 2007

Publication title -

chemistry – a european journal

Language(s) - English

Resource type - Reports

SCImago Journal Rank - 1.687

H-Index - 242

eISSN - 1521-3765

pISSN - 0947-6539

DOI - 10.1002/chem.200790027

Subject(s) - diastereomer , cover (algebra) , conformational isomerism , chemistry , clips , computational chemistry , combinatorial chemistry , stereochemistry , computer science , molecule , organic chemistry , artificial intelligence , mechanical engineering , engineering

Chiral molecular clips were separated by HPLC, and their CD spectra are shown on the cover. These clips, the pseudoenantiomers anti ‐ 1 and anti ‐ 2 , and diastereomer syn ‐ 3 , were used for assignment of the absolute configurations of anti ‐ 1 and anti ‐ 2 . The space‐filling structures of anti ‐ 1 and anti ‐ 2 , also shown, were calculated by conducting a Monte‐Carlo conformer search using the force field MMFF94 implemented in SPARTAN '04. For more details, see the Full Paper by Y. Inoue, F.‐G. Klärner et al. on page 2473 ff.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research