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The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate

Samo za registrovane korisnike
1965
Autori
Mihailović, Milhailo Lj.
Stojiljković, A.
Andrejević, Vladimir
Članak u časopisu (Objavljena verzija)
Metapodaci
Prikaz svih podataka o dokumentu
Apstrakt
The only amino compounds oxidized so far with lead tetroacetate were primary aromatic amines, which gave mainly the corresponding azo compounds(1), and some tertiary aryldialkyl amines, which in glacial acetic acid in the presence of acetic acid anhydride underwent oxidative dealkylation with the formation of acetylated secondary amines (2).
Ključne reči:
unbranched primary alkyl / arylalkyl amines / lead tetraacetate / oxidation
Izvor:
Tetrahedron Letters, 1965, 6, 8, 461-464
Izdavač:
  • Elsevier

DOI: 10.1016/S0040-4039(00)89979-7

ISSN: 0040-4039; 1873-3581

Scopus: 2-s2.0-50549200778
[ Google Scholar ]
12
URI
https://cer.ihtm.bg.ac.rs/handle/123456789/4655
Kolekcije
  • Radovi istraživača / Researchers' publications
Institucija/grupa
IHTM
TY  - JOUR
AU  - Mihailović, Milhailo Lj.
AU  - Stojiljković, A.
AU  - Andrejević, Vladimir
PY  - 1965
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4655
AB  - The only amino compounds oxidized so far with lead tetroacetate were primary aromatic amines, which gave mainly the corresponding azo compounds(1), and some tertiary aryldialkyl amines, which in glacial acetic acid in the presence of acetic acid anhydride underwent oxidative dealkylation with the formation of acetylated secondary amines (2).
PB  - Elsevier
T2  - Tetrahedron Letters
T1  - The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate
VL  - 6
IS  - 8
SP  - 461
EP  - 464
DO  - 10.1016/S0040-4039(00)89979-7
ER  - 
@article{
author = "Mihailović, Milhailo Lj. and Stojiljković, A. and Andrejević, Vladimir",
year = "1965",
abstract = "The only amino compounds oxidized so far with lead tetroacetate were primary aromatic amines, which gave mainly the corresponding azo compounds(1), and some tertiary aryldialkyl amines, which in glacial acetic acid in the presence of acetic acid anhydride underwent oxidative dealkylation with the formation of acetylated secondary amines (2).",
publisher = "Elsevier",
journal = "Tetrahedron Letters",
title = "The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate",
volume = "6",
number = "8",
pages = "461-464",
doi = "10.1016/S0040-4039(00)89979-7"
}
Mihailović, M. Lj., Stojiljković, A.,& Andrejević, V.. (1965). The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate. in Tetrahedron Letters
Elsevier., 6(8), 461-464.
https://doi.org/10.1016/S0040-4039(00)89979-7
Mihailović ML, Stojiljković A, Andrejević V. The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate. in Tetrahedron Letters. 1965;6(8):461-464.
doi:10.1016/S0040-4039(00)89979-7 .
Mihailović, Milhailo Lj., Stojiljković, A., Andrejević, Vladimir, "The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate" in Tetrahedron Letters, 6, no. 8 (1965):461-464,
https://doi.org/10.1016/S0040-4039(00)89979-7 . .

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