Asymmetric Syntheses V: Asymmetric Alkylation of D-Camphor Imine of 1-Aminomethyl Naphthalene
- 1 April 1989
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 19 (7-8) , 1297-1302
- https://doi.org/10.1080/00397918908054537
Abstract
Alkylation of the D-camphor imine of 1-amino-methyl naphthalene with a variety of alkylating agents gave diastereoselectivities ranging from 20–64%. The de ratio in the alkylation could be determined by the chemical shift difference of 1H-NMR signals of the C-8 methyl groups or by 13C-NMR signals in the C-7 of compound (6).Keywords
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