Chiral 8-amino substituted 2-phenyl-5,6,7,8-tetrahydro-6,6-dimethylmethanoquinolines as chiral ligands for enantioselective catalysis: palladium catalysed allylic substitution and addition of diethylzinc to benzaldehyde

doi:10.1016/S0957-4166(97)00275-9

Paper

Chiral 8-amino substituted 2-phenyl-5,6,7,8-tetrahydro-6,6-dimethylmethanoquinolines as chiral ligands for enantioselective catalysis: palladium catalysed allylic substitution and addition of diethylzinc to benzaldehyde

Published Aug 14, 1997 · G. Chelucci, G. Pinna, A. Saba

Tetrahedron-asymmetry

UNKNOWN SJR score

25

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Chiral 8-amino substituted 2-phenyl-5,6,7,8-tetrahydro-6,6-dimethylmethanoquinolines show enantioselectivity up to 68% in palladium catalyzed allylic substitution and diethylzinc

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Chiral 8-amino substituted 2-phenyl-5,6,7,8-tetrahydro-6,6-dimethylmethanoquinolines as chiral ligands for enantioselective catalysis: palladium catalysed allylic substitution and addition of diethylzinc to benzaldehyde

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