Tetrahedron Letters
CC-connective synthesis of α-dialkylamino-ketones from aldehydes and sec.-amines
D Enders, H Lotter
Index: Enders, Dieter; Lotter, Hermann Tetrahedron Letters, 1982 , vol. 23, # 6 p. 639 - 642
Full Text: HTML
Citation Number: 21
Abstract
Abstract A simple and efficient 3-step synthesis of α-dialkylamino-ketones 3 starting from aldehydes and sec.-amines is described. The unsymmetrically aminoketones are obtained as pure regioisomers via reaction of metalated α-aminonitriles 1 with aldehydes, followed by thermal HCN-elimination/tautomerization.
Related Articles:
The reductive coupling of tertiary amides to give enediamines using PhMe 2 SiLi
[Fleming, Ian; Ghosh, Usha; Mack, Stephen R.; Clark, Barry P. Chemical Communications, 1998 , # 6 p. 711 - 712]