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• W2550124937 abstract "In this work the synthesis of new asymmetric diamine ligands from camphoric acid is described. The new diamines can be directly prepared in a regioselective arylation of the less hindered primary amine group of (+)-cis-1,2,2-trimethylcyclopentane-1,3-diamine via a Buchwald–Hartwig amination in high yields. The resulting diamines incorporate a secondary and primary amine group and were successfully applied as ligands in a copper-catalyzed Henry reaction. Copyright © 2014 John Wiley & Sons, Ltd." @default.
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• W2550124937 date "2014-05-29" @default.
• W2550124937 modified "2023-10-07" @default.
• W2550124937 title "Highly regioselective synthesis of chiral diamines via a Buchwald-Hartwig amination from camphoric acid and their application in the Henry reaction" @default.
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• W2550124937 doi "https://doi.org/10.1002/aoc.3162" @default.
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