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Volumn 14, Issue 15, 2008, Pages 4600-4617

Symmetrically tetrasubstituted [2.2]paracyclophanes: Their systematization and regioselective synthesis of several types of bis-bifunctional derivatives by double electrophilic substitution

Author keywords

Asymmetric catalysis; Cyclophanes; Electrophilic substitution; Regioselectivity; Resolution

Indexed keywords

ASYMMETRIC CATALYSIS; CYCLOPHANES; ELECTROPHILIC SUBSTITUTION; REGIOSELECTIVITY; RESOLUTION;

EID: 53849126861     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200701683     Document Type: Article
Times cited : (69)

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    • The symmetry properties of several [2.2]paracyclophanes mono-, diand tetrasubstituted in aromatic rings and ethano bridges were illustrated by Cram with co-authors, using as examples the respective bromides which were obtaind in their group at the time: D. J. Cram, R. B. Hornby, E. A. Truesdale, H. J. Reich, M. H. Delton, J. M. Cram, Tetrahedron 1974, 30, 1757-1768.
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    • p] for description of the interior of the paracyclophanyl fragment in the respective chiral and achiral di- and tetrasubstituted derivatives.
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