4, 4′-Di-tert-butylbiphenyl-catalysed reductive opening of azetidines with lithium: A direct preparation of 3, N-dilithioalkylamines
J Almena, F Foubelo, M Yus
Index: Almena, Juan; Foubelo, Francisco; Yus, Miguel Tetrahedron, 1994 , vol. 50, # 19 p. 5775 - 5782
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Citation Number: 50
Abstract
The reaction of N-phenylazetidine 1a with an excess of lithium powder and a catalytic amount of 4, 4′-di-tert-butylbiphenyl (5 mol%) in THF at− 15° C leads to the corresponding dianion 2a, which by treatment with different electrophiles (H2O, D2O, ButCHO, PhCHO,(CH 2) 5C O, PhCH NPh, CO2) yields, after hydrolysis with water, the expected functionalysed amines 3aa-ah. The same method applied to N-isopropyl-2-phenylazetidine 1 c affords ...
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