Synthesis, resolution and rates of racemisation of 1-(2'-methyl-3'- indenyl)-2-naphthylamine and -2-naphthol

Tetrahedron Letters

Volumn 41, Issue 22, 2000, Pages 4471-4473

  Baker, Robert W ^a   Taylor, James A ^a  

^a UNIVERSITY OF SYDNEY   (Australia)

Author keywords

Axial chirality; Circular dichroism; Indenes; Planar chirality

Indexed keywords

1 NAPHTHOL DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; CIRCULAR DICHROISM; ENANTIOMER; STEREOCHEMISTRY; SYNTHESIS; THERMOSTABILITY;

EID: 0034622065     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)00618-3     Document Type: Article

References (6)

1. Halterman, R. L. Chem. Rev. 1992, 92, 965, and references cited therein.
2. Baker, R. W.; Wallace, B. J. Chem. Commun. 1999, 1405.
3. Baker, R. W.; Wallace, B. J.; Turner, P. J. Chem. Soc., Dalton Trans. 2000, 431.
4. R: 19.2 min for (aR)-7 and 21.6 min for (aS)-7, 18.6 min for (aR)-8 and 25.3 min for (aS)-8.
5. Baker, R. W.; Reek, J. N. H.; Wallace, B. J. Tetrahedron Lett. 1998, 39, 6573.
6. R: 6.0 min for (aR)-7 and 6.6 min for (aS)-7, 11.4 min for (aR)-8 and 12.9 min for (aS)-8.