Aminoacetals. Syntheses of N,N-Disubstituted 4-Amino-2- butynal- and 4-Aminobutanal- acetals
D. Keglević
; Tracer Laboratory, Institute »Ruder Boskovic«, Zagreb, Croatia, Yugoslavia
B. Leonhard
; Tracer Laboratory, Institute »Ruder Boskovic«, Zagreb, Croatia, Yugoslavia
APA 6th Edition Keglević, D. i Leonhard, B. (1963). Aminoacetals. Syntheses of N,N-Disubstituted 4-Amino-2- butynal- and 4-Aminobutanal- acetals. Croatica Chemica Acta, 35 (3), 175-181. Preuzeto s https://hrcak.srce.hr/208335
MLA 8th Edition Keglević, D. i B. Leonhard. "Aminoacetals. Syntheses of N,N-Disubstituted 4-Amino-2- butynal- and 4-Aminobutanal- acetals." Croatica Chemica Acta, vol. 35, br. 3, 1963, str. 175-181. https://hrcak.srce.hr/208335. Citirano 07.03.2021.
Chicago 17th Edition Keglević, D. i B. Leonhard. "Aminoacetals. Syntheses of N,N-Disubstituted 4-Amino-2- butynal- and 4-Aminobutanal- acetals." Croatica Chemica Acta 35, br. 3 (1963): 175-181. https://hrcak.srce.hr/208335
Harvard Keglević, D., i Leonhard, B. (1963). 'Aminoacetals. Syntheses of N,N-Disubstituted 4-Amino-2- butynal- and 4-Aminobutanal- acetals', Croatica Chemica Acta, 35(3), str. 175-181. Preuzeto s: https://hrcak.srce.hr/208335 (Datum pristupa: 07.03.2021.)
Vancouver Keglević D, Leonhard B. Aminoacetals. Syntheses of N,N-Disubstituted 4-Amino-2- butynal- and 4-Aminobutanal- acetals. Croatica Chemica Acta [Internet]. 1963 [pristupljeno 07.03.2021.];35(3):175-181. Dostupno na: https://hrcak.srce.hr/208335
IEEE D. Keglević i B. Leonhard, "Aminoacetals. Syntheses of N,N-Disubstituted 4-Amino-2- butynal- and 4-Aminobutanal- acetals", Croatica Chemica Acta, vol.35, br. 3, str. 175-181, 1963. [Online]. Dostupno na: https://hrcak.srce.hr/208335. [Citirano: 07.03.2021.]
Sažetak The synthesis of N,N-disubstituted 4-aminobutanal acetals
(XV - XXII) was effected by the hydrogenation of the corresponding
acetylenic analogues. N,N-Disubstituted 4-amino-2-
-butynal acetals (IV-XII) were prepared by the Mannich condensation
of propargylaldehyde acetal, formaldehyde and the corresponding
secondary amine. As an alternative route to N,N-
disubstituted acetylenic aminoacetals, Bodroux-Tschitschibabin
acetal synthesis was also applied in the preparation of 4-dibenzylamino-
2-butynal ac et al (VII).