Regioselective 1,4-conjugate aza-Michael addition of dienones with benzotriazole
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AbstractThe regioselective 1,4-conjugate aza-Michael addition of dienones with benzotriazole catalyzed by potassium acetate is described. A series of 3-(benzotriazol-1-yl)-1,5-diarylpent-4-en-1-ones were efficiently synthesized under mild conditions. This protocol has advantages of transition-metal free catalyst, high yield and high regioselectivity.
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2017 ◽
Vol 359
(23)
◽
pp. 4197-4207
◽
2021 ◽
pp. 1-13
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