Journal
ORGANIC LETTERS
Volume 20, Issue 22, Pages 7034-7038Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b02967
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A stereoselective domino inverse electron demand Diels-Alder/amine group transfer reaction catalyzed by a bidentate Lewis acid provides 1-amino-1,2-dihydronaphthalenes, a core structure in many bioactive compounds. A concerted mechanism is proposed based on experimental studies as well as DFT computations demonstrating a new general reactivity scheme. The broad scope of the reaction was evaluated by variation of all three starting compounds, phthalazines, aldehydes, and amines. Scalability was demonstrated by a gram scale reaction without diminished yield.
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