Asymmetric 1, 3-dipolar cycloadditions of a chiral non-racemic azomethine imineo

Tetrahedron Letters

Volumn 40, Issue 19, 1999, Pages 3727-3730

  Roussi, Fanny ^a   Bonin, Martine ^a   Chiaroni, Angèle ^b   Micouin, Laurent ^a   Riche, Claude ^b   Husson, Henri Philippe ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AZOMETHINE AMINE; BENZALDEHYDE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; COMPLEX FORMATION; MOLECULAR INTERACTION; SYNTHESIS;

EID: 0033532220     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00610-3     Document Type: Article

References (21)

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19. +).
20. [8]. Surprisingly, an exo selectivity, based on NMR considerations, has been recently described for very similar adducts in racemic series : see ref. 6a.
21. -3. In the packing of the molecules, only normal Van der Waals contacts are observed. Lists of the fractional atomic coordinates, thermal parameters, distances, bond and torsion angles have been deposited at the Cambridge Crystallographic Data Centre, U.K., as Supplementary Material (CIF file).