Synthesis and absolute configuration of a bi[10]paracyclophane with two chiral planes and one chiral axis

Tetrahedron Asymmetry

Volumn 10, Issue 1, 1999, Pages 21-24

  Tochtermann, Werner ^a   Kuckling, Dirk ^a   Meints, Christine ^a   Kraus, Jürgen ^b   Bringmann, Gerhard ^b  

^a UNIVERSITY OF KIEL   (Germany)

^b UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PARACYCLOPHANE DERIVATIVE;

ARTICLE; CIRCULAR DICHROISM; ENANTIOMER; PRIORITY JOURNAL; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0033556675     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(98)00500-X     Document Type: Article

References (14)

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8. Tochtermann, W.; Haase, M. Chem. Ber. 1984, 117, 2293-2299.
9. Review: von Angerer, S.; Tochtermann, W. In Methods Org. Chem. (Houben-Weyl); 4th edn, Vol. E 9d, 1998; pp. 1-64.
10. Peters, K.; Peters, E.-M.; Karl, B.; Tochtermann, W. Z. Kristallogr., NCS, 1997, 212, 369-370.
11. Peters, K.; Peters, E.-M.; Vanselow, B.; Tochtermann, W. Z. Kristallogr., NCS, 1998, 213, 93-94, 95-96.
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13. Review: Bringmann, G.; Busemann, S. In Natural Product Analysis; Schreier, P.; Herderich, M.; Humpf, H. U.; Schwab, W., Eds; Vieweg: Braunschweig, 1998; pp. 195-212.
14. meso-Tartaric acid likewise prefers chiral conformations, which, however, equilibrate rapidly at ambient temperature because of low energy rotation barriers: Ascenso, J.; Gil, V. M. S. Can. J. Chem. 1980, 58, 1376-1379 and literature cited therein.